Difference between revisions of "YGL213C"
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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. | ||
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Revision as of 13:02, 21 February 2007
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Systematic name | YGL213C |
Gene name | SKI8 |
Aliases | REC103 |
Feature type | ORF, Verified |
Coordinates | Chr VII:91251..90058 |
Description of YGL213C: Protein involved in exosome mediated 3' to 5' mRNA degradation and translation inhibition of non-poly(A) mRNAs as well as double-strand break formation during meiotic recombination; required for repressing propagation of dsRNA viruses[1][2][3][4]
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Contents
Community Commentary
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Interactions
Two Hybrid
Two Hybrid interaction with spo11
[1] [5]
Protein Details
Protein Localization
cytoplasmic localization during vegetative growth, relocalizes to nucleus and onto chromosomes during meiosis [1] [5]
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References
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- ↑ 1.0 1.1 1.2 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
- ↑ Anderson JS and Parker RP (1998) The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex. EMBO J 17(5):1497-506 SGD PMID 9482746
- ↑ Masison DC, et al. (1995) Decoying the cap- mRNA degradation system by a double-stranded RNA virus and poly(A)- mRNA surveillance by a yeast antiviral system. Mol Cell Biol 15(5):2763-71 SGD PMID 7739557
- ↑ Brown JT, et al. (2000) The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo. RNA 6(3):449-57 SGD PMID 10744028
- ↑ 5.0 5.1 submitted by Scott Keeney on 2004-05-02
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