The serine protease Omi/HtrA2 regulates apoptosis by binding XIAP through a reaper-like motif.
The inhibitor-of-apoptosis proteins (IAPs) play a critical role in the regulation of apoptosis by binding and inhibiting caspases. Reaper family proteins and Smac/DIABLO use a conserved amino-terminal sequence to bind to IAPs in flies and mammals, respectively, blocking their ability to inhibit caspases and thus promoting apoptosis. Here we have identified the serine protease Omi/HtrA2 as a second mammalian XIAP-binding protein with a Reaper-like motif. This protease autoprocesses to form a protein with amino-terminal homology to Smac/DIABLO and Reaper family proteins. Full-length Omi/HtrA2 is localized to mitochondria but fails to interact with XIAP. Mitochondria also contain processed Omi/HtrA2, which, following apoptotic insult, translocates to the cytosol, where it interacts with XIAP. Overexpression of Omi/HtrA2 sensitizes cells to apoptosis, and its removal by RNA interference reduces cell death. Omi/HtrA2 thus extends the set of mammalian proteins with Reaper-like function that are released from the mitochondria during apoptosis.
Pubmed ID: 11602612 RIS Download
Amino Acid Motifs | Amino Acid Sequence | Apoptosis | Binding Sites | Drosophila Proteins | Humans | Mitochondria | Mitochondrial Proteins | Molecular Sequence Data | Peptides | Proteins | Serine Endopeptidases | X-Linked Inhibitor of Apoptosis Protein