半胱氨酸蛋白酶
DNA损伤
战斗或逃跑反应
细胞生物学
化学
细胞凋亡
细胞应激反应
癌症研究
生物
生物化学
DNA
程序性细胞死亡
基因
作者
Antoine Tinel,Jürg Tschopp
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-04-13
卷期号:304 (5672): 843-846
被引量:655
标识
DOI:10.1126/science.1095432
摘要
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.
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