| Literature DB >> 18591963 |
Bicheng Zhang1, Jun Huang, Hong-Liang Li, Ting Liu, Yan-Yi Wang, Paul Waterman, Ai-Ping Mao, Liang-Guo Xu, Zhonghe Zhai, Depei Liu, Philippa Marrack, Hong-Bing Shu.
Abstract
Here, we report the identification of GIDE, a mitochondrially located E3 ubiquitin ligase. GIDE contains a C-terminal RING finger domain, which is mostly conserved with those of the IAP family members and is required for GIDE's E3 ligase activity. Overexpression of GIDE induces apoptosis via a pathway involving activation of caspases, since caspase inhibitors, XIAP and an inactive mutant of caspase-9 block GIDE-induced apoptosis. GIDE also activates JNK, and blockage of JNK activation inhibits GIDE-induced release of cytochrome c and Smac as well as apoptosis, suggesting that JNK activation precedes release of cytochrome c and Smac and is required for GIDE-induced apoptosis. These pro-apoptotic properties of GIDE require its E3 ligase activity. When somewhat over- or underexpressed, GIDE slows or accelerates cell growth, respectively. These pro-apoptotic or growth inhibition effects of GIDE may account for its absence in tumor cells.Entities:
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Year: 2008 PMID: 18591963 PMCID: PMC3156110 DOI: 10.1038/cr.2008.75
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617