Difference between revisions of "Commonly used auxotrophic markers"
(Table edited by Maria via TableEdit) |
(Table edited by Maria via TableEdit) |
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TGG-to-TGA nonsense change at codon 244; | TGG-to-TGA nonsense change at codon 244; | ||
− | GGA-to-GAA missense change at codon 185 | + | GGA-to-GAA missense change at codon 185 |
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[http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000060944 Nakayashiki et al. 2001] | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000060944 Nakayashiki et al. 2001] | ||
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[http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000049198 Engebrecht and Roeder 1990] | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000049198 Engebrecht and Roeder 1990] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=can1 can1-100] | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | yes | ||
+ | | | ||
+ | ochre mutation | ||
+ | | | ||
+ | AAA-to-TAA ochre nonsense change at codon 47 | ||
+ | | | ||
+ | Rodney Rothstein, [http://wiki.yeastgenome.org/index.php/CommunityW303.html Personal communication to SGD] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=his3 his3delta200] | ||
+ | | | ||
+ | yes | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | Cold sensitive; high frequency of petite formation, especially during transformation. Note that this deletion damages the PET56 promoter. See [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000074003 Zhang et al. (2003)] for a discussion of this issue. | ||
+ | | | ||
+ | 1 kb deletion (-205 to 835) | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042846 Struhl 1985]; [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000046453 Fasullo and Davis 1988] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=his3 his3delta1] | ||
+ | | | ||
+ | partial | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | |||
+ | | | ||
+ | 187 bp HindIII-HindIII internal deletion (305 to 492) | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000040818 Scherer and Davis 1979] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=his3 his3-11,15] | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | double mutant | ||
+ | | | ||
+ | G deletion at nucleotide 208, | ||
+ | G deletion at nucleotide 319 | ||
+ | | | ||
+ | Rodney Rothstein, [http://wiki.yeastgenome.org/index.php/CommunityW303.html Personal communication to SGD] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=leu2 leu2delta1] | ||
+ | | | ||
+ | partial | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | |||
+ | | | ||
+ | EcoRI-ClaI internal deletion (163 to 649, 0.6 kb) | ||
+ | | | ||
+ | [www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski and Hieter 1989] | ||
+ | |- | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/locus.fpl?locus=leu2 leu2-3,112] | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | no | ||
+ | | | ||
+ | double mutant | ||
+ | | | ||
+ | GTC-to-GTT silent change at codon 56, | ||
+ | GTT-to-GCT missense change at codon 69, | ||
+ | G insertion at nucleotide 249, | ||
+ | G insertion at nucleotide 792, | ||
+ | GTT-to-GTC silent change at codon 299, | ||
+ | GAC-to-AAC missense change at codon 300 | ||
+ | | | ||
+ | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000043265 Hinnen et al. 1978]; | ||
+ | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000042541 Gaber and Culbertson 1982]; | ||
+ | [http://www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000069760 Meira LB et al., 1995]; | ||
+ | [http://wiki.yeastgenome.org/index.php/CommunityW303.html Rodney Rothstein, Personal communication to SGD] | ||
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Revision as of 10:35, 8 March 2012
This table describes some commonly used auxotrophic markers (along with some novel useful markers); it is based on a table in Brachmann et al. (1998) "Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications." Yeast 14:115-132. Please send e-mail to the curators at SGD at sgd-helpdesk@lists.stanford.edu if you have additions or modifications you would like to suggest.
<protect>
Allele | Deleted ORF? | Reverts? | Notes | Molecular Descriptiona | Reference |
---|---|---|---|---|---|
no |
yes |
red colonies |
TGG-to-TGA nonsense change at codon 244; GGA-to-GAA missense change at codon 185 |
||
no |
yes |
ochre mutation |
TTA-to-TTG silent change at codon 9, GAA-to-TAA ochre nonsense change at codon 64, AGA-to-GGA missense change at codon 101, GTT-to-GTC silent change at codon 124, ACG-to-ACA silent change at codon 539 |
Rodney Rothstein, Personal communication to SGD | |
no |
yes |
ochre mutation, red colonies |
G to T transversion at nucleotide 190, changing codon 64 from a Glu to a Stop |
||
no |
no |
red colonies |
frameshift (BglII site filled in at position 592) |
||
no |
yes |
ochre mutation |
AAA-to-TAA ochre nonsense change at codon 47 |
Rodney Rothstein, Personal communication to SGD | |
yes |
no |
Cold sensitive; high frequency of petite formation, especially during transformation. Note that this deletion damages the PET56 promoter. See Zhang et al. (2003) for a discussion of this issue. |
1 kb deletion (-205 to 835) |
||
partial |
no |
187 bp HindIII-HindIII internal deletion (305 to 492) |
|||
no |
no |
double mutant |
G deletion at nucleotide 208, G deletion at nucleotide 319 |
Rodney Rothstein, Personal communication to SGD | |
partial |
no |
EcoRI-ClaI internal deletion (163 to 649, 0.6 kb) |
[www.yeastgenome.org/cgi-bin/reference/reference.pl?dbid=S000044428 Sikorski and Hieter 1989] | ||
no |
no |
double mutant |
GTC-to-GTT silent change at codon 56, GTT-to-GCT missense change at codon 69, G insertion at nucleotide 249, G insertion at nucleotide 792, GTT-to-GTC silent change at codon 299, GAC-to-AAC missense change at codon 300 |
Hinnen et al. 1978; Gaber and Culbertson 1982; Meira LB et al., 1995; Rodney Rothstein, Personal communication to SGD | |
edit table |
</protect>
aThe sequence coordinates are relative to the first ATG of the selectable marker ORF, in which the A residue is defined as +1.
bAll trp- strains are cold sensitive (Singh and Manney 1974).