Difference between revisions of "YDR369C"
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| + | Specifically higher expression in carbon limited chemostat cultures versus carbon excess. | ||
| + | <ref>Boer VM, et al. (2003) The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur. | ||
| + | J Biol Chem 278(5):3265-74</ref> | ||
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Revision as of 13:02, 21 February 2007
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| Systematic name | YDR369C |
| Gene name | XRS2 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr IV:1217572..1215008 |
Description of YDR369C: Protein required for DNA repair; component of the Mre11 complex, which is involved in double strand breaks, meiotic recombination, telomere maintenance, and checkpoint signaling[1][2][3]
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Community Commentary
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Interactions
Two Hybrid
Two Hybrid interaction with Rec107
[4] [5]
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References
See Help:References on how to add references
- ↑ Usui T, et al. (1998) Complex formation and functional versatility of Mre11 of budding yeast in recombination. Cell 95(5):705-16 SGD PMID 9845372
- ↑ Bressan DA, et al. (1999) The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae. Mol Cell Biol 19(11):7681-7 SGD PMID 10523656
- ↑ Ivanov EL, et al. (1992) XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination. Genetics 132(3):651-64 SGD PMID 1468624
- ↑ Arora C, et al. (2004) Antiviral protein Ski8 is a direct partner of Spo11 in meiotic DNA break formation, independent of its cytoplasmic role in RNA metabolism. Mol Cell 13(4):549-59 SGD PMID 14992724
- ↑ submitted by Scott Keeney on 2004-05-02
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