Difference between revisions of "YJR094C"

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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates'''
 
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates'''
|nowrap| Chr X:605647..604565
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|nowrap| Chr X:605643..604561
 
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID'''          || S000003854
 
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID'''          || S000003854
 
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'''Description of YJR094C:''' Master regulator of meiosis that is active only during meiotic events, activates transcription of early meiotic genes through interaction with Ume6p, degraded by the 26S proteasome following phosphorylation by Ime2p<ref name='S000073063'>Kassir Y, et al. (2003) Transcriptional regulation of meiosis in budding yeast. Int Rev Cytol 224():111-71 {{SGDpaper|S000073063}} PMID 12722950</ref><ref name='S000069718'>Guttmann-Raviv N, et al. (2002) Ime2, a meiosis-specific kinase in yeast, is required for destabilization of its transcriptional activator, Ime1. Mol Cell Biol 22(7):2047-56
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'''Description of YJR094C:''' Master regulator of meiosis that is active only during meiotic events, activates transcription of early meiotic genes through interaction with Ume6p, degraded by the 26S proteasome following phosphorylation by Ime2p<ref name='S000073063'>Kassir Y, et al. (2003) Transcriptional regulation of meiosis in budding yeast. Int Rev Cytol 224:111-71 {{SGDpaper|S000073063}} PMID 12722950</ref><ref name='S000069718'>Guttmann-Raviv N, et al. (2002) Ime2, a meiosis-specific kinase in yeast, is required for destabilization of its transcriptional activator, Ime1. Mol Cell Biol 22(7):2047-56
 
  {{SGDpaper|S000069718}} PMID 11884593</ref>
 
  {{SGDpaper|S000069718}} PMID 11884593</ref>
 
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Revision as of 07:21, 26 February 2009

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Systematic name YJR094C
Gene name IME1
Aliases
Feature type ORF, Verified
Coordinates Chr X:605643..604561
Primary SGDID S000003854


Description of YJR094C: Master regulator of meiosis that is active only during meiotic events, activates transcription of early meiotic genes through interaction with Ume6p, degraded by the 26S proteasome following phosphorylation by Ime2p[1][2]




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DNA and RNA Details

Other DNA and RNA Details

Other Topic: expression

Specifically higher expression in carbon limited chemostat cultures versus carbon excess. [3] [4]





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References

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  1. Kassir Y, et al. (2003) Transcriptional regulation of meiosis in budding yeast. Int Rev Cytol 224:111-71 SGD PMID 12722950
  2. Guttmann-Raviv N, et al. (2002) Ime2, a meiosis-specific kinase in yeast, is required for destabilization of its transcriptional activator, Ime1. Mol Cell Biol 22(7):2047-56 SGD PMID 11884593
  3. 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 SGD PMID 12414795
  4. submitted by Viktor Boer on 2003-07-25

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