Difference between revisions of "YIR005W"
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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 | YIR005W |
| Gene name | IST3 |
| Aliases | SNU17 |
| Feature type | ORF, Verified |
| Coordinates | Chr IX:364886..365332 |
Description of YIR005W: Component of the U2 snRNP, required for the first catalytic step of splicing and for spliceosomal assembly; interacts with Rds3p and is required for Mer1p-activated splicing[1][2][3]
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Contents
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References
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- ↑ Spingola M, et al. (2004) Mer1p is a modular splicing factor whose function depends on the conserved U2 snRNP protein Snu17p. Nucleic Acids Res 32(3):1242-50 SGD PMID 14973223
- ↑ Wang Q and Rymond BC (2003) Rds3p is required for stable U2 snRNP recruitment to the splicing apparatus. Mol Cell Biol 23(20):7339-49 SGD PMID 14517302
- ↑ Gottschalk A, et al. (2001) A novel yeast U2 snRNP protein, Snu17p, is required for the first catalytic step of splicing and for progression of spliceosome assembly. Mol Cell Biol 21(9):3037-46 SGD PMID 11287609
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