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		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384573</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384573"/>
		<updated>2012-08-02T09:09:44Z</updated>

		<summary type="html">&lt;p&gt;Mralser: /* W303-K6001 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology. The Sigma278b genome is closely related to S288c, and shares some other genomic regions with W303 [http://dx.doi.org/10.1098/rsob.120093].&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table style=&amp;quot;text-align: left; width: 526px; height: 174px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
cellpadding=&amp;quot;2&amp;quot; cellspacing=&amp;quot;2&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;allele&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;locus&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;mutation [http://dx.doi.org/10.1098/rsob.120093 (1)] &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;ade2-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YOR128C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu64STOP&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;trp1-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YDR007W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu83STOP&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;can1-100 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YEL063C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, lys47&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;leu2-3,112 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YCL018W &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, gly83&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;his3-11,15 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YOR202W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; 2x frameshifts, ala70 and glu106&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' The W303 genome is to 85.4% derived from S288c, part of the other regions are similar to non-S288c regions of Sigma1278b.  In total, some 800 CDS differ between W303 and S288c, but in most cases only one or two residues differ [http://dx.doi.org/10.1098/rsob.120093]. These include a ''bud4'' mutation that causes haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute] and by Ralser et al &amp;lt;i&amp;gt;Open Biol 2: 120093.&lt;br /&gt;
[http://dx.doi.org/10.1098/rsob.120093 1] &amp;lt;/i&amp;gt; (DDBJ/EMBL/GenBank ALAV00000000).  &lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was created in Kim Nasmyth's lab ''Piatti at al'' (PMID: 7641697) and ''Bobola et al'' (PMID: 8625408). K6001 has become a popular model in yeast aging research, as it allows a replicative aging assay based on microcolonies (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566), Ralser et al [http://dx.doi.org/10.1098/rsob.120093].&lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
Sources: ATCC: 28383&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;br /&gt;
&lt;br /&gt;
=Y55=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a /''MAT''alpha   ''HO''/''HO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Y55 is a prototrophic, homothallic diploid strain that was originally isolated by Dennis Winge. Many auxotrophic mutant derivatives have been created by John McCusker by using ethidium bromide treatment to eliminate non-auxotrophs. Y55 background strains have been used to study the timing of meiotic recombination ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000148282 Borts et al. 1984]); to isolate almost all the subunits of the proteasome ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294104 McCusker and Haber 1988a], [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294103 1988b]); to get mutations in PMA1 and related genes ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=2963211 McCusker 1986]); and to do meiotic mapping and interference experiments ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=15454526 Malkova et al. 2004]).&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
	<entry>
		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384572</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384572"/>
		<updated>2012-08-02T09:08:43Z</updated>

		<summary type="html">&lt;p&gt;Mralser: /* W303-K6001 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology. The Sigma278b genome is closely related to S288c, and shares some other genomic regions with W303 [http://dx.doi.org/10.1098/rsob.120093].&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table style=&amp;quot;text-align: left; width: 526px; height: 174px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
cellpadding=&amp;quot;2&amp;quot; cellspacing=&amp;quot;2&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;allele&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;locus&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;mutation [http://dx.doi.org/10.1098/rsob.120093 (1)] &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;ade2-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YOR128C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu64STOP&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;trp1-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YDR007W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu83STOP&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;can1-100 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YEL063C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, lys47&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;leu2-3,112 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YCL018W &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, gly83&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;his3-11,15 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YOR202W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; 2x frameshifts, ala70 and glu106&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' The W303 genome is to 85.4% derived from S288c, part of the other regions are similar to non-S288c regions of Sigma1278b.  In total, some 800 CDS differ between W303 and S288c, but in most cases only one or two residues differ [http://dx.doi.org/10.1098/rsob.120093]. These include a ''bud4'' mutation that causes haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute] and by Ralser et al &amp;lt;i&amp;gt;Open Biol 2: 120093.&lt;br /&gt;
[http://dx.doi.org/10.1098/rsob.120093 1] &amp;lt;/i&amp;gt; (DDBJ/EMBL/GenBank ALAV00000000).  &lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was created in Kim Nasmyth's lab ''Piatti at al'' (PMID: 7641697) and ''Bobola et al'' (PMID: 8625408). K6001 has become a popular model in yeast aging research, as it allows a replicative aging assay based on microcolonies (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566) and Ralser et al.&lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
Sources: ATCC: 28383&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;br /&gt;
&lt;br /&gt;
=Y55=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a /''MAT''alpha   ''HO''/''HO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Y55 is a prototrophic, homothallic diploid strain that was originally isolated by Dennis Winge. Many auxotrophic mutant derivatives have been created by John McCusker by using ethidium bromide treatment to eliminate non-auxotrophs. Y55 background strains have been used to study the timing of meiotic recombination ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000148282 Borts et al. 1984]); to isolate almost all the subunits of the proteasome ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294104 McCusker and Haber 1988a], [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294103 1988b]); to get mutations in PMA1 and related genes ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=2963211 McCusker 1986]); and to do meiotic mapping and interference experiments ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=15454526 Malkova et al. 2004]).&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
	<entry>
		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384571</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384571"/>
		<updated>2012-08-02T09:04:24Z</updated>

		<summary type="html">&lt;p&gt;Mralser: /* Sigma 1278B */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology. The Sigma278b genome is closely related to S288c, and shares some other genomic regions with W303 [http://dx.doi.org/10.1098/rsob.120093].&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table style=&amp;quot;text-align: left; width: 526px; height: 174px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
cellpadding=&amp;quot;2&amp;quot; cellspacing=&amp;quot;2&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;allele&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;locus&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;mutation [http://dx.doi.org/10.1098/rsob.120093 (1)] &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;ade2-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YOR128C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu64STOP&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;trp1-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YDR007W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu83STOP&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;can1-100 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YEL063C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, lys47&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;leu2-3,112 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YCL018W &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, gly83&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;his3-11,15 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YOR202W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; 2x frameshifts, ala70 and glu106&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' The W303 genome is to 85.4% derived from S288c, part of the other regions are similar to non-S288c regions of Sigma1278b.  In total, some 800 CDS differ between W303 and S288c, but in most cases only one or two residues differ [http://dx.doi.org/10.1098/rsob.120093]. These include a ''bud4'' mutation that causes haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute] and by Ralser et al &amp;lt;i&amp;gt;Open Biol 2: 120093.&lt;br /&gt;
[http://dx.doi.org/10.1098/rsob.120093 1] &amp;lt;/i&amp;gt; (DDBJ/EMBL/GenBank ALAV00000000).  &lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was developed by ''Bobola et al'' in Kim Nasmyth's lab (PMID: 8625408), and has become a common model in yeast aging research (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566)&lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
Sources: ATCC: 28383&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;br /&gt;
&lt;br /&gt;
=Y55=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a /''MAT''alpha   ''HO''/''HO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Y55 is a prototrophic, homothallic diploid strain that was originally isolated by Dennis Winge. Many auxotrophic mutant derivatives have been created by John McCusker by using ethidium bromide treatment to eliminate non-auxotrophs. Y55 background strains have been used to study the timing of meiotic recombination ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000148282 Borts et al. 1984]); to isolate almost all the subunits of the proteasome ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294104 McCusker and Haber 1988a], [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294103 1988b]); to get mutations in PMA1 and related genes ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=2963211 McCusker 1986]); and to do meiotic mapping and interference experiments ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=15454526 Malkova et al. 2004]).&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
	<entry>
		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384570</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384570"/>
		<updated>2012-08-02T09:01:15Z</updated>

		<summary type="html">&lt;p&gt;Mralser: /* W303 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology.&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
&amp;lt;table style=&amp;quot;text-align: left; width: 526px; height: 174px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
cellpadding=&amp;quot;2&amp;quot; cellspacing=&amp;quot;2&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;allele&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;locus&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-weight: bold;&amp;quot;&amp;gt;mutation [http://dx.doi.org/10.1098/rsob.120093 (1)] &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;ade2-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YOR128C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu64STOP&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;trp1-1&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YDR007W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;nonsense, glu83STOP&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;can1-100 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; YEL063C&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, lys47&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;leu2-3,112 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YCL018W &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;frameshift, gly83&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;tr&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top; font-style: italic;&amp;quot;&amp;gt;his3-11,15 &amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt;YOR202W&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;td style=&amp;quot;vertical-align: top;&amp;quot;&amp;gt; 2x frameshifts, ala70 and glu106&amp;lt;/td&amp;gt;&lt;br /&gt;
&amp;lt;/tr&amp;gt;&lt;br /&gt;
&amp;lt;/table&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' The W303 genome is to 85.4% derived from S288c, part of the other regions are similar to non-S288c regions of Sigma1278b.  In total, some 800 CDS differ between W303 and S288c, but in most cases only one or two residues differ [http://dx.doi.org/10.1098/rsob.120093]. These include a ''bud4'' mutation that causes haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute] and by Ralser et al &amp;lt;i&amp;gt;Open Biol 2: 120093.&lt;br /&gt;
[http://dx.doi.org/10.1098/rsob.120093 1] &amp;lt;/i&amp;gt; (DDBJ/EMBL/GenBank ALAV00000000).  &lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was developed by ''Bobola et al'' in Kim Nasmyth's lab (PMID: 8625408), and has become a common model in yeast aging research (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566)&lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
Sources: ATCC: 28383&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;br /&gt;
&lt;br /&gt;
=Y55=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a /''MAT''alpha   ''HO''/''HO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Y55 is a prototrophic, homothallic diploid strain that was originally isolated by Dennis Winge. Many auxotrophic mutant derivatives have been created by John McCusker by using ethidium bromide treatment to eliminate non-auxotrophs. Y55 background strains have been used to study the timing of meiotic recombination ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000148282 Borts et al. 1984]); to isolate almost all the subunits of the proteasome ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294104 McCusker and Haber 1988a], [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294103 1988b]); to get mutations in PMA1 and related genes ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=2963211 McCusker 1986]); and to do meiotic mapping and interference experiments ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=15454526 Malkova et al. 2004]).&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
	<entry>
		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384569</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=384569"/>
		<updated>2012-08-02T08:43:14Z</updated>

		<summary type="html">&lt;p&gt;Mralser: /* W303 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology.&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''In total, some 800 CDS differ between W303 and S288c, but in most cases only one or two aa are exchanged [http://dx.doi.org/10.1098/rsob.120093]. These include a ''bud4'' mutation that causes haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute] and by Ralser et al &amp;lt;i&amp;gt;Open Biol 2: 120093.&lt;br /&gt;
[http://dx.doi.org/10.1098/rsob.120093 1] &amp;lt;/i&amp;gt; (DDBJ/EMBL/GenBank ALAV00000000). The W303 genome is to 85.4% derived from S288c, other regions are partly overlapping with non-S288c regions of Sigma1278b. &lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was developed by ''Bobola et al'' in Kim Nasmyth's lab (PMID: 8625408), and has become a common model in yeast aging research (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566)&lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
Sources: ATCC: 28383&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;br /&gt;
&lt;br /&gt;
=Y55=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a /''MAT''alpha   ''HO''/''HO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Y55 is a prototrophic, homothallic diploid strain that was originally isolated by Dennis Winge. Many auxotrophic mutant derivatives have been created by John McCusker by using ethidium bromide treatment to eliminate non-auxotrophs. Y55 background strains have been used to study the timing of meiotic recombination ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000148282 Borts et al. 1984]); to isolate almost all the subunits of the proteasome ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294104 McCusker and Haber 1988a], [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=3294103 1988b]); to get mutations in PMA1 and related genes ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=2963211 McCusker 1986]); and to do meiotic mapping and interference experiments ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=15454526 Malkova et al. 2004]).&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
	<entry>
		<id>https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=275094</id>
		<title>Commonly used strains</title>
		<link rel="alternate" type="text/html" href="https://wiki.yeastgenome.org/index.php?title=Commonly_used_strains&amp;diff=275094"/>
		<updated>2011-01-13T11:45:15Z</updated>

		<summary type="html">&lt;p&gt;Mralser: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;This page describes some of the most commonly used yeast lab strains. Much of the information is taken from [http://dbb.urmc.rochester.edu/labs/sherman_f/StartedYeast.html F. Sherman (2002)] Getting started with yeast, Methods Enzymol. 350, 3-41. Other useful papers for strain background information include:&lt;br /&gt;
&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43 - thoroughly describes the genealogy of strain S288C&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714 - compares various characteristics of commonly used lab strains&lt;br /&gt;
* [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080159 Winzeler et al.] (2003) Genetics 163:79-89 - uses SFP (single-feature polymorphisms) analysis to study genetic identity between common lab strains&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=S288C=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''SUC2 gal2 mal mel flo1 flo8-1 hap1 ho bio1 bio6''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the systematic sequencing project, the sequence stored in SGD. S288C does not form pseudohyphae. In addition, since it has a mutated copy of [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000004246 ''HAP1''], it is not a good strain for mitochondrial studies. It has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. S288C strains are ''gal''2- and they do not use galactose anaerobically.&lt;br /&gt;
&lt;br /&gt;
The S288C genome was recently resequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] (1986) Genetics 113:35-43.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204508&amp;amp;Template=yeastGeneticStock ATCC:204508]&lt;br /&gt;
&lt;br /&gt;
==BY4743==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''his3''&amp;amp;#x394;''1/his3''&amp;amp;#x394;''1 leu2''&amp;amp;#x394;''0/leu2''&amp;amp;#x394;''0 LYS2/lys2''&amp;amp;#x394;''0 met15''&amp;amp;#x394;''0/MET15 ura3''&amp;amp;#x394;''0/ura3''&amp;amp;#x394;''0''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Strain used in the [http://www-sequence.stanford.edu/group/yeast_deletion_project/project_desc.html systematic deletion project], generated from a cross between BY4741 and BY4742, which are derived from S288C. As S288c, these strains have an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. See Brachmann et al. reference for details.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041186 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1050|Open Biosystems:YSC1050]&lt;br /&gt;
&lt;br /&gt;
==FY4==&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=9483801 Brachmann et al.] (1998) Yeast 14:115-32.&lt;br /&gt;
&lt;br /&gt;
==FY1679==&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 trp1''&amp;amp;#x394;''63/TRP1 leu2''&amp;amp;#x394;''1/LEU2 his3''&amp;amp;#x394;''200/HIS3 GAL2/GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''  Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000047446 Winston et al.] (1995) Yeast 11:53-55.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/fy1679.html EUROSCARF:10000D]&lt;br /&gt;
&lt;br /&gt;
==AB972==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1;'' X2180-1B trp1&amp;lt;sub&amp;gt;0&amp;lt;/sub&amp;gt; [rho &amp;lt;sup&amp;gt;0&amp;lt;/sup&amp;gt;]''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD. AB972 is an ethidium bromide-induced rho- derivative of the strain X2180-1B-''trp1''.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000057090 Olson MV et al.] (1986) Proc. Natl. Acad. Sci. USA 83:7826-7830.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204511&amp;amp;Template=yeastGeneticStock ATCC:204511]&lt;br /&gt;
&lt;br /&gt;
==A364A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' ade1 ade2 ura1 his7 lys2 tyr1 gal1 SUC mal cup BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079649 Hartwell] (1967) J. Bacteriol. 93:1662-1670.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=208526&amp;amp;Template=yeastGeneticStock ATCC:208526]&lt;br /&gt;
&lt;br /&gt;
==XJ24-24a==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ho HMa HM&amp;amp;#x3B1; ade6 arg4-17 trp1-1 tyr7-1 MAL2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Derived from, but not isogenic to, S288C&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000055409 Strathern et al.] (1979) Cell 18:309-319&lt;br /&gt;
&lt;br /&gt;
==DC5==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' leu2-3,112 his3-11,15 can1-11''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Isogenic to S288C; used in the systematic sequencing project, the sequence stored in SGD.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054242 Broach et al.] (1979) Gene 8:121-133&lt;br /&gt;
&lt;br /&gt;
==X2180-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a'' SUC2 mal mel gal2 CUP1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''S288c spontaneously diploidized to give rise to X2180. The haploid segregants X2180-1a and X2180-1b were obtained from sporulated X2180&lt;br /&gt;
&lt;br /&gt;
'''References:'''  [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000050744 Mortimer and Johnston] &lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204504&amp;amp;Template=yeastGeneticStock ATCC:204504]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=YNN216=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt;/lys2-801&amp;lt;sup&amp;gt;amber&amp;lt;/sup&amp;gt; ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;/ade2-101&amp;lt;sup&amp;gt;ochre&amp;lt;/sup&amp;gt;''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Congenic to S288C (see Sikorski and Hieter). Used to derive YSS and CY strains (see Sobel and Wolin).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&lt;br /&gt;
==YPH499==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Contains nonrevertible (deletion) auxotrophic mutations that can be used for selection of vectors. Note that ''trp1-''&amp;amp;#x394;''63'', unlike ''trp1-''&amp;amp;#x394;''1'', does not delete adjacent ''GAL3'' UAS sequence and retains homology to ''TRP1'' selectable marker. ''gal2-'', does not use galactose anaerobically. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204679&amp;amp;Template=yeastGeneticStock ATCC:204679]&lt;br /&gt;
&lt;br /&gt;
==YPH500==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''ura3-52 lys2-801_amber ade2-101_ochre trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:'''''MAT''&amp;amp;#x3B1; strain isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] except at mating type locus. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204680&amp;amp;Template=yeastGeneticStock ATCC:204680]&lt;br /&gt;
&lt;br /&gt;
==YPH501==&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''ura3-52/ura3-52 lys2-801_amber/lys2-801_amber ade2-101_ochre/ade2-101_ochre trp1-''&amp;amp;#x394;''63/trp1-''&amp;amp;#x394;''63 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 leu2-''&amp;amp;#x394;''1/leu2-''&amp;amp;#x394;''1''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' a/&amp;amp;#x3B1; diploid isogenic to [http://staff.yeastgenome.org/index.php/straintable#yph499 YPH499] and [http://staff.yeastgenome.org/index.php/straintable#yph500 YPH500]. Derived from the diploid strain YNN216 (Johnston and Davis 1984; original source: M. Carlson, Columbia University), which is congenic with S288C.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski RS and Hieter P] (1989) Genetics 122:19-27.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042217 Sobel and Wolin] (1999) Mol. Biol. Cell 10:3849-3862.&amp;lt;br /&amp;gt;[http://db.yeastgenome.org/cgi-bin/reference/reference.pl?pubmed=6092912 Johnston M and Davis RW] (1984) Mol Cell Biol 4(8):1440-8.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204681&amp;amp;Template=yeastGeneticStock ATCC:204681]&lt;br /&gt;
&lt;br /&gt;
=Sigma 1278B=&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Used in pseudohyphal growth studies. [[History_of_Sigma|Detailed notes]] about the sigma strains have been kindly provided by Cora Styles.&lt;br /&gt;
&lt;br /&gt;
[http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1000823 Granek and Magwene], PLoS Genet. 2010 Jan 22;6(1):e1000823, established that certain lineages of the Sigma1278B background contain&lt;br /&gt;
a nonsense mutation in RIM15, a G-to-T transversion at position 1216 that converts a Gly codon to an opal stop codon. This rim15 mutation interacts epistatically with mutations in certain other genes to affect colony morphology.&lt;br /&gt;
&lt;br /&gt;
Annotation of the Sigma1278b genome and information about the systematic deletion collection can be found [http://mcdb.colorado.edu/labs1/dowelllab/pubs/DowellRyan/ here].&lt;br /&gt;
&lt;br /&gt;
=SK1=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' HO gal2 cup&amp;lt;sup&amp;gt;S&amp;lt;/sup&amp;gt; can1&amp;lt;sup&amp;gt;R&amp;lt;/sup&amp;gt; BIO''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Commonly used for studying sporulation or meiosis. Canavanine-resistant derivative.&lt;br /&gt;
&lt;br /&gt;
The SK1 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079650 Kane SM and Roth J.] (1974) Bacteriol. 118: 8-14&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=204722&amp;amp;Template=yeastGeneticStock ATCC:204722]&lt;br /&gt;
&lt;br /&gt;
=CEN.PK (aka CEN.PK2)=&lt;br /&gt;
'''Genotype:''' ''MAT''a/&amp;amp;#x3B1;'' ura3-52/ura3-52 trp1-289/trp1-289 leu2-3_112/leu2-3_112 his3 ''&amp;amp;#x394;''1/his3 ''&amp;amp;#x394;''1 MAL2-8C/MAL2-8C SUC2/SUC2''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' CEN.PK  possesses a mutation in CYR1 (A5627T corresponding to a K1876M substitution near the end of the catalytic domain in adenylate cyclase which eliminates glucose- and acidification-induced cAMP signalling and delays glucose-induced loss of stress resistance ([http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000052724 Vanhalewyn et al., 1999]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043601 Dumortier et al., 2000]).&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000079648 van Dijken et al.] (2000) Enzyme Microb Technol 26:706-714&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://web.uni-frankfurt.de/fb15/mikro/euroscarf/data/cen.html EUROSCARF:30000D]&lt;br /&gt;
&lt;br /&gt;
=W303=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''} [''phi&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;'']&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303 also contains a ''bud4'' mutation that causes&lt;br /&gt;
haploids to bud with a mixture of axial and bipolar budding&lt;br /&gt;
patterns. In addition, the original W303 strain contains the&lt;br /&gt;
''rad5-535'' allele. As S288c, W303 has an allelic variant of [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=MIP1 ''MIP1''] which increases petite frequency. &lt;br /&gt;
&lt;br /&gt;
The W303 genome was sequenced at the [http://www.sanger.ac.uk/Teams/Team118/sgrp/ Sanger Institute].&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''bud4'' info: [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000120449 Voth  et al.] (2005) Eukaryotic Cell, 4:1018-28.&amp;lt;br /&amp;gt;''rad5-535'' info: Fan et al. (1996) Genetics 142:749&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1A==&lt;br /&gt;
'''Genotype:''' ''MAT''a {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' W303-1A possesses a ''ybp1-1'' mutation (I7L, F328V, K343E, N571D) which abolishes Ybp1p function, increasing sensitivity to oxidative stress.&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&amp;lt;br /&amp;gt;''ybp1-1'' info: [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000073844 Veal et al.] (2003) J. Biol. Chem. 278:30896-904.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-1B==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; {''leu2-3,112 trp1-1 can1-100 ura3-1 ade2-1 his3-11,15''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' W303 constructed by Rodney Rothstein (''see [[CommunityW303.html|detailed notes]] from RR and Stephan Bartsch'').&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.openbiosystems.com/Query/?i=0&amp;amp;q=YSC1058|Open Biosystems:YSC1058]&lt;br /&gt;
&lt;br /&gt;
==W303-K6001==&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a; {''ade2-1, trp1-1, can1-100, leu2-3,112, his3-11,15, GAL, psi+, ho::HO::CDC6 (at HO), cdc6::hisG, ura3::URA3 GAL-ubiR-CDC6 (at URA3)''}&lt;br /&gt;
&lt;br /&gt;
'''References:''' K6001 was developed by ''Bobola et al'' in Kim Nasmyth's lab (PMID: 8625408), and has become a common model in yeast aging research (PMID: 15489200). Its genome has been sequenced by Timmermann et al (PMID: 20729566) &lt;br /&gt;
&lt;br /&gt;
=D273-10B=&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''mal''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' Normal cytochrome content and respiration; low frequency of rho-. This strain and its auxotrophic derivatives were used in numerious laboratories for mitochondrial and related studies and for mutant screens. Good respirer that's relatively resistant to glucose repression.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000080158 Sherman, F.] (1963) Genetics 48:375-385.&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=24657&amp;amp;Template=fungiYeast ATCC:24657]&lt;br /&gt;
&lt;br /&gt;
=FL100=&lt;br /&gt;
'''Genotype:''' ''MAT''a&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000065623 Lacroute, F.] (1968) J. Bacteriol. 95:824-832.&lt;br /&gt;
&lt;br /&gt;
=SEY6210/SEY6211=&lt;br /&gt;
'''Genotype:''' ''MAT''a/''MAT''&amp;amp;#x3B1; ''leu2-3,112/leu2-3,112 ura3-52/ura3-52 his3-''&amp;amp;#x394;''200/his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901/trp1-''&amp;amp;#x394;''901 ade2/ADE2 suc2-''&amp;amp;#x394;''9/suc2-''&amp;amp;#x394;''9 GAL/GAL LYS2/lys2-801''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210/SEY6211, also known as SEY6210.5, was constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers, good growth properties and good sporulation.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=201392&amp;amp;Template=fungiYeast ATCC:201392]&lt;br /&gt;
&lt;br /&gt;
==SEY6210==&lt;br /&gt;
'''Genotype:''' ''MAT''&amp;amp;#x3B1; ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 suc2-''&amp;amp;#x394;''9 lys2-801; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6210 is a MATalpha haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96099&amp;amp;Template=fungiYeast ATCC:96099]&lt;br /&gt;
&lt;br /&gt;
==SEY6211==&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2-3,112 ura3-52 his3-''&amp;amp;#x394;''200 trp1-''&amp;amp;#x394;''901 ade2-101 suc2-''&amp;amp;#x394;''9; GAL''&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' SEY6211 is a MATa haploid constructed by Scott Emr and has been used in studies of autophagy, protein sorting etc. It is the product of crossing with strains from 5 different labs (Gerry Fink, Ron Davis, David Botstein, Fred Sherman, Randy Schekman). It has several selectable markers and good growth properties.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000045321 Robinson et al.] (1988) Mol Cell Biol 8(11):4936-48&lt;br /&gt;
&lt;br /&gt;
'''Sources:''' [http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=96100&amp;amp;Template=fungiYeast ATCC:96100]&lt;br /&gt;
&lt;br /&gt;
=JK9-3d=&lt;br /&gt;
&lt;br /&gt;
There are a, alpha and a/alpha diploids of JK9-3d with the following genotypes:&lt;br /&gt;
&lt;br /&gt;
'''Genotypes:''' JK9-3da  ''MAT''a ''leu2-3,112 ura3-52 rme1 trp1 his4''&lt;br /&gt;
&lt;br /&gt;
JK9-3d&amp;amp;#x3B1; has the same genotype as JK9-3da with the exception of the MAT locus&lt;br /&gt;
&lt;br /&gt;
JK9-3da/&amp;amp;#x3B1; is homozygous for all markers except mating type&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' JK9-3d was constructed by Jeanette Kunz while in Mike Hall's lab. She made the original strain while Joe Heitman isolated isogenic strains of opposite mating type and&lt;br /&gt;
derived the a/alpha isogenic diploid by mating type switching.  It has in its background S288c, a strain from the Oshima lab, and a strain from the Herskowitz lab. It was chosen because of its robust growth and sporulation, as well as good growth on galactose (GAL+) (so that genes under control of the galactose promoter could be induced). It may also have a SUP mutation that allows translation through premature STOP codons and therefore produces functional alleles with many point mutations.&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054286 Heitman et al.] (1991a) Science 253(5022):905-9 and [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000054822 Heitman et al.] (1991b) Proc Natl Acad Sci U S A 88(5):1948-52&lt;br /&gt;
&lt;br /&gt;
=RM11-1a=&lt;br /&gt;
&lt;br /&gt;
'''Genotype:''' ''MAT''a ''leu2''&amp;amp;#x394;'' ura3''&amp;amp;#x394;'' ho::Kan&lt;br /&gt;
&lt;br /&gt;
'''Notes:''' RM11-1a is a haploid derivative of Bb32(3), a natural isolate collected by Robert Mortimer from a California vineyard, as in [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000041556 Mortimer et al., 1994]. It has high spore viability (80–90%) and has been extensively characterized phenotypically under a wide range of conditions. It has a significantly longer life span than typical lab yeast strains and accumulates age-associated abnormalities at a lower rate. It displays approximately 0.5–1% sequence divergence relative to S288c. More information is available at the [http://www.broad.mit.edu/annotation/genome/saccharomyces_cerevisiae.3/Home.html Broad Institute website].&lt;br /&gt;
&lt;br /&gt;
'''References:''' [http://db.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069875 Brem et al.] (2002) Science 296(5568):752-5&lt;/div&gt;</summary>
		<author><name>Mralser</name></author>
		
	</entry>
</feed>