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A serine protease, HtrA2, is released from the mitochondria and interacts with XIAP, inducing cell death



A serine protease, HtrA2, is released from the mitochondria and interacts with XIAP, inducing cell death



Molecular Cell 8(3): 613-621



X chromosome-linked inhibitor of apoptosis (XIAP) is an endogenous inhibitor of caspase-3, -7, and -9. Smac/DIABLO, an inhibitor of XIAP, is released from mitochondria upon receiving apoptotic stimuli and binds to the BIR2 and BIR3 domains of XIAP, thereby inhibiting its caspase-inhibitory activity. Here we report that a serine protease called HtrA2/Omi is released from mitochondria and inhibits the function of XIAP by direct binding in a similar way to Smac. Moreover, when overexpressed extramitochondrially, HtrA2 induces atypical cell death, which is neither accompanied by a significant increase in caspase activity nor inhibited by caspase inhibitors, including XIAP. A catalytically inactive mutant of HtrA2, however, does not induce cell death. In short, HtrA2 is a Smac-like inhibitor of IAP activity with a serine protease-dependent cell death-inducing activity.

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Accession: 010097263

Download citation: RISBibTeXText

PMID: 11583623

DOI: 10.1016/s1097-2765(01)00341-0


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