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.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Apoptosis* / drug effects
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Caspase Inhibitors
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Cell Line
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Cell Proliferation / drug effects
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Enzyme Activation / drug effects
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Gene Expression Profiling
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Humans
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Inhibitor of Apoptosis Proteins / metabolism
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JNK Mitogen-Activated Protein Kinases
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MAP Kinase Kinase Kinases / metabolism
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Mice
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Mitochondria / drug effects
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Mitochondria / enzymology*
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Molecular Sequence Data
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NIH 3T3 Cells
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Protease Inhibitors / pharmacology
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Protein Transport / drug effects
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Transcription Factors / chemistry
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Transcription Factors / genetics
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Transcription Factors / metabolism*
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Transfection
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Ubiquitin-Protein Ligases / chemistry
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Ubiquitin-Protein Ligases / genetics
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Ubiquitin-Protein Ligases / metabolism*
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Ubiquitination / drug effects
Substances
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Caspase Inhibitors
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Inhibitor of Apoptosis Proteins
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Protease Inhibitors
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Transcription Factors
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MUL1 protein, human
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Ubiquitin-Protein Ligases
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JNK Mitogen-Activated Protein Kinases
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MAP Kinase Kinase Kinases
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MAP kinase kinase kinase 7