Difference between revisions of "YLR426W"

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(Add data on a YLR426 knock-out strain's growth in complete media)
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J Biol Chem 278(5):3265-74</ref>
 
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===[[UW-Stout/Salt_Concentration_SP21|Salt Concentration (NaCl)]]===
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[[Image:NaCl-BY4735vYLR426W-Graph.JPG]]
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0mM NaCl conc. BY4735 strain's doubling time: 169 minutes
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0mM NaCl conc. YLR426W strain's doubling time: 481 minutes
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750mM NaCl conc. BY4735 strain's doubling time: 294 minutes
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750mM NaCl conc. YLR426W strain's doubling time: 909 minutes
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The graph above shows the growth rate for the previously listed strains and the relative level of NaCl concentration. Comparing the YLR426W doubling times between 0mM and 750mM NaCl, there is a tremendous effect on the growth rate. This effect negatively influences the knockout strain's (YLR426W) growth rate.
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Revision as of 09:39, 27 April 2021

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Systematic name YLR426W
Gene name TDA5
Aliases
Feature type ORF, Uncharacterized
Coordinates Chr XII:987062..988113
Primary SGDID S000004418


Description of YLR426W: Putative protein of unknown function; detected in highly purified mitochondria in high-throughput studies; proposed to be involved in resistance to mechlorethamine and streptozotocin; null mutant sensitive to expression of top1-T722A allele[1][2][3][4]




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Community Commentary

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This gene is part of the UW-Stout Orphan Gene Project. Learn more here.

Growth Curve

YLR426W-water.png

In a BY4735 background, knocking out YLR426W seems to have a substantial effect on the strain's growth in complete media. In this assay, the BY4735 strain's doubling time was 162 minutes, while the YLR426W knock-out strain's doubling time was 660 minutes. (These doubling times are the means of three experiments.)




Salt Concentration (NaCl)

NaCl-BY4735vYLR426W-Graph.JPG


0mM NaCl conc. BY4735 strain's doubling time: 169 minutes

0mM NaCl conc. YLR426W strain's doubling time: 481 minutes

750mM NaCl conc. BY4735 strain's doubling time: 294 minutes

750mM NaCl conc. YLR426W strain's doubling time: 909 minutes


The graph above shows the growth rate for the previously listed strains and the relative level of NaCl concentration. Comparing the YLR426W doubling times between 0mM and 750mM NaCl, there is a tremendous effect on the growth rate. This effect negatively influences the knockout strain's (YLR426W) growth rate.




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References

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  1. Lee W, et al. (2005) Genome-wide requirements for resistance to functionally distinct DNA-damaging agents. PLoS Genet 1(2):e24 SGD PMID 16121259
  2. Reid RJ, et al. (2011) Selective ploidy ablation, a high-throughput plasmid transfer protocol, identifies new genes affecting topoisomerase I-induced DNA damage. Genome Res 21(3):477-86 SGD PMID 21173034
  3. Reinders J, et al. (2006) Toward the complete yeast mitochondrial proteome: multidimensional separation techniques for mitochondrial proteomics. J Proteome Res 5(7):1543-54 SGD PMID 16823961
  4. Sickmann A, et al. (2003) The proteome of Saccharomyces cerevisiae mitochondria. Proc Natl Acad Sci U S A 100(23):13207-12 SGD PMID 14576278

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