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Publication : Mdm2 targets the p53 transcription cofactor JMY for degradation.

First Author  Coutts AS Year  2007
Journal  EMBO Rep Volume  8
Issue  1 Pages  84-90
PubMed ID  17170761 Mgi Jnum  J:148063
Mgi Id  MGI:3843429 Doi  10.1038/sj.embor.7400855
Citation  Coutts AS, et al. (2007) Mdm2 targets the p53 transcription cofactor JMY for degradation. EMBO Rep 8(1):84-90
abstractText  We define here a new mechanism through which Mdm2 (mouse double minute 2) regulates p53 activity, by targeting the p53 transcription cofactor JMY. DNA damage causes an increase in JMY protein, and, in a similar manner, small molecule inhibitors of Mdm2 activity induce JMY in unperturbed cells. At a mechanistic level, Mdm2 regulation of JMY requires the Mdm2 RING (really interesting new gene) finger, which promotes the ubiquitin-dependent degradation of JMY. However, regulation of JMY occurs independently of the p53-binding domain in Mdm2 and p53 activity. These results define a new functional relationship between the p53 cofactor JMY and Mdm2, and indicate that transcription cofactors that facilitate p53 activity are important targets for Mdm2 in suppressing the p53 response.
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