Difference between revisions of "YJR021C"

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Specifically higher expression in carbon limited chemostat cultures versus carbon excess.
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<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.
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J Biol Chem 278(5):3265-74</ref>
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Revision as of 12:02, 21 February 2007

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Systematic name YJR021C
Gene name REC107
Aliases MER2
Feature type ORF, Verified
Coordinates Chr X:469572..468548


Description of YJR021C: Protein involved in early stages of meiotic recombination; involved in altering chromatin structure at DNA double-stranded break sites and in coordination between the initiation of recombination and the first division of meiosis[1][2][3]




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Interactions

Two Hybrid

Two Hybrid interaction with Mei4, Xrs2
[4] [5]


Two Hybrid interaction with Rec114
Meiosis-specific two hybrid interaction [4] [5]


Two Hybrid interaction with Rec114
Meiosis-specific two hybrid interaction [4] [5]


Two Hybrid interaction with Rec114
Meiosis-specific two hybrid interaction [4] [5]




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References

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  1. Malone RE, et al. (2004) The signal from the initiation of meiotic recombination to the first division of meiosis. Eukaryot Cell 3(3):598-609 SGD PMID 15189982
  2. Malone RE, et al. (1991) Isolation of mutants defective in early steps of meiotic recombination in the yeast Saccharomyces cerevisiae. Genetics 128(1):79-88 SGD PMID 2060778
  3. Ohta K, et al. (1998) Mutations in the MRE11, RAD50, XRS2, and MRE2 genes alter chromatin configuration at meiotic DNA double-stranded break sites in premeiotic and meiotic cells. Proc Natl Acad Sci U S A 95(2):646-51 SGD PMID 9435246
  4. 4.0 4.1 4.2 4.3 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
  5. 5.0 5.1 5.2 5.3 submitted by Scott Keeney on 2004-05-02

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