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      Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition.

      Cell
      Adult, Amino Acid Sequence, Apoptosis, Apoptotic Protease-Activating Factor 1, Base Sequence, Carrier Proteins, Caspase 3, Caspase 9, Caspases, metabolism, Cloning, Molecular, Cytochrome c Group, Cytosol, DNA, Complementary, Enzyme Activation, Enzyme Precursors, HeLa Cells, Humans, Intracellular Signaling Peptides and Proteins, Mitochondria, Mitochondrial Proteins, Molecular Sequence Data, Protein Processing, Post-Translational, Protein Sorting Signals, Proteins, genetics, isolation & purification, Radiation Tolerance, Ultraviolet Rays, X-Linked Inhibitor of Apoptosis Protein

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          Abstract

          We report here the identification of a novel protein, Smac, which promotes caspase activation in the cytochrome c/Apaf-1/caspase-9 pathway. Smac promotes caspase-9 activation by binding to inhibitor of apoptosis proteins, IAPs, and removing their inhibitory activity. Smac is normally a mitochondrial protein but is released into the cytosol when cells undergo apoptosis. Mitochondrial import and cleavage of its signal peptide are required for Smac to gain its apoptotic activity. Overexpression of Smac increases cells' sensitivity to apoptotic stimuli. Smac is the second mitochondrial protein, along with cytochrome c, that promotes apoptosis by activating caspases.

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