(Q27626899)

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J W Wu

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S Kyin

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X Wang

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Y Shi

Mechanisms and genes of cellular suicide

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language of work or name

English

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publication date

24 August 2000

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published in

Nature

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volume

406

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issue

6798

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page(s)

855-62

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cites work

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The Drosophila caspase inhibitor DIAP1 is essential for cell survival and is negatively regulated by HID.

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Induction of apoptosis by Drosophila reaper, hid and grim through inhibition of IAP function

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Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome c-dependent activation of caspase-3

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Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade

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Autoactivation of procaspase-9 by Apaf-1-mediated oligomerization

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Essential role of CED-4 oligomerization in CED-3 activation and apoptosis

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WD-40 repeat region regulates Apaf-1 self-association and procaspase-9 activation

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An APAF-1.cytochrome c multimeric complex is a functional apoptosome that activates procaspase-9

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Cytochrome c and dATP-mediated oligomerization of Apaf-1 is a prerequisite for procaspase-9 activation

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

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Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins

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Cleavage of human inhibitor of apoptosis protein XIAP results in fragments with distinct specificities for caspases

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A single BIR domain of XIAP sufficient for inhibiting caspases

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The 40-kDa subunit of DNA fragmentation factor induces DNA fragmentation and chromatin condensation during apoptosis

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Extent of N-terminal methionine excision from Escherichia coli proteins is governed by the side-chain length of the penultimate amino acid

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