Peer-Reviewed Journal Details
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Srinivasula SM;Gupta S;Datta P;Zhang Z;Hegde R;Cheong N;Fernandes-Alnemri T;Alnemri ES;
2003
August
Journal Of Biological Chemistry
Inhibitor of apoptosis proteins are substrates for the mitochondrial serine protease Omi/HtrA2.
Published
Optional Fields
278
34
The mature serine protease Omi/HtrA2 is released from the mitochondria into the cytosol during apoptosis. Suppression of Omi/HtrA2 by RNA interference in human cell lines reduces cell death in response to TRAIL and etoposide. In contrast, ectopic expression of mature wildtype Omi/HtrA2, but not an active site mutant, induces potent caspase activation and apoptosis. In vitro assays demonstrated that Omi/HtrA2 could degrade inhibitor of apoptosis proteins (IAPs). Consistent with this observation, increased expression of Omi/HtrA2 in cells increases degradation of XIAP, while suppression of Omi/HtrA2 by RNA interference has an opposite effect. Combined, our data demonstrate that IAPs are substrates for Omi/HtrA2, and their degradation could be a mechanism by which the mitochondrially released Omi/HtrA2 activates caspases during apoptosis.
0021-9258
10.1074/jbc.C300240200
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