GIDE is a mitochondrial E3 ubiquitin ligase that induces apoptosis and slows growth

  • Cell Res. 2008 Sep;18(9):900-10. doi: 10.1038/cr.2008.75.
Bicheng Zhang  1 ,  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
Affiliations
  • 1. HHMI, National Jewish Medical and Research Center, Denver, CO 80206, USA.
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.