Difference between revisions of "YHR086W"
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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 | YHR086W |
| Gene name | NAM8 |
| Aliases | MRE2, MUD15 |
| Feature type | ORF, Verified |
| Coordinates | Chr VIII:278155..279726 |
Description of YHR086W: RNA binding protein, component of the U1 snRNP protein; mutants are defective in meiotic recombination and in formation of viable spores, involved in the formation of DSBs through meiosis-specific splicing of MER2 pre-mRNA[1][2][3]
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References
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- ↑ Ogawa H, et al. (1995) Functions of the yeast meiotic recombination genes, MRE11 and MRE2. Adv Biophys 31():67-76 SGD PMID 7625279
- ↑ Puig O, et al. (1999) Interaction of the U1 snRNP with nonconserved intronic sequences affects 5' splice site selection. Genes Dev 13(5):569-80 SGD PMID 10072385
- ↑ Nakagawa T and Ogawa H (1997) Involvement of the MRE2 gene of yeast in formation of meiosis-specific double-strand breaks and crossover recombination through RNA splicing. Genes Cells 2(1):65-79 SGD PMID 9112441
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