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The PIDDosome, a protein complex implicated in activation of caspase-2 in response to genotoxic stress

机译:PIDDosome,一种蛋白质复合物,与基因毒性胁迫相关,可激活caspase-2

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Apoptosis is triggered by activation of initiator caspases upon complex-mediated clustering of the inactive zymogen, as occurs in the caspase-9 activating apoptosome complex. Likewise, caspase-2, which is involved in stress-induced apoptosis, is recruited into a large protein complex, the molecular composition of which remains elusive. We show that activation of caspase-2 occurs in a complex that contains the death domain - containing protein PIDD, whose expression is induced by p53, and the adaptor protein RAIDD. Increased PIDD expression resulted in spontaneous activation of caspase-2 and sensitization to apoptosis by genotoxic stimuli. Because PIDD functions in p53-mediated apoptosis, the complex assembled by PIDD and caspase-2 is likely to regulate apoptosis induced by genotoxins.
机译:凋亡是由复合物介导的无活性酶原团簇的激活引起的胱天蛋白酶激活引起的,就像激活caspase-9的凋亡小体复合物一样。同样,参与应激诱导的细胞凋亡的caspase-2被募集到大分子蛋白质复合物中,其分子组成仍然难以捉摸。我们显示caspase-2的激活发生在包含死亡域的复合物中-包含蛋白PIDD(其表达由p53诱导)和衔接蛋白RAIDD。 PIDD表达的增加导致caspase-2的自发激活和遗传毒性刺激对凋亡的敏感性。因为PIDD在p53介导的凋亡中起作用,所以PIDD和caspase-2组装的复合物很可能调节由基因毒素诱导的凋亡。

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