| Literature DB >> 17535800 |
Traci R Lyons1, Jackie Thorburn, Philip W Ryan, Andrew Thorburn, Steven M Anderson, C Kenneth Kassenbrock.
Abstract
POSH (Plenty of SH3 domains) binds to activated Rac and promotes apoptosis by acting as a scaffold to assemble a signal transduction pathway leading from Rac to JNK activation. Overexpression of POSH induces apoptosis in a variety of cell types, but apoptosis can be prevented by co-expressing the pro-survival protein kinase Akt. We report here that POSH is a direct substrate for phosphorylation by Akt in vivo and in vitro, and we identify a major site of Akt phosphorylation as serine 304 of POSH, which lies within the Rac-binding domain. We further show that phosphorylation of POSH results in a decreased ability to bind activated Rac, as does phosphomimetic S304D and S304E mutation of POSH. S304D mutant POSH also shows a strongly reduced ability to induce apoptosis. These findings identify a novel mechanism by which Akt promotes cell survival.Entities:
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Year: 2007 PMID: 17535800 DOI: 10.1074/jbc.M704321200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157