• Title of article

    Smac, a Mitochondrial Protein that Promotes Cytochrome c–Dependent Caspase Activation by Eliminating IAP Inhibition

  • Author/Authors

    Chunying Du، نويسنده , , Min Fang، نويسنده , , Yucheng Li and Bin Teng، نويسنده , , M. Lily Li، نويسنده , , Xiaodong Wang، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2000
  • Pages
    10
  • From page
    33
  • To page
    42
  • 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 i nhibitor of a poptosis p roteins, 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 cellsʹ sensitivity to apoptotic stimuli. Smac is the second mitochondrial protein, along with cytochrome c, that promotes apoptosis by activating caspases.
  • Journal title
    CELL
  • Serial Year
    2000
  • Journal title
    CELL
  • Record number

    1017024