Suppression of apoptosis signal-regulating kinase 1-induced cell death by 14-3-3 proteins

被引:297
作者
Zhang, LX
Chen, J
Fu, HA [1 ]
机构
[1] Emory Univ, Dept Pharmacol, Atlanta, GA 30322 USA
[2] Emory Univ, Grad Program Biochem Cell & Dev Biol, Atlanta, GA 30322 USA
关键词
D O I
10.1073/pnas.96.15.8511
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Apoptosis signal-regulating kinase 1 (ASK1) is a pivotal component of a signaling pathway induced by many death stimuli, including tumor necrosis factor alpha, Fas, and the anticancer drugs cisplatin and paclitaxel, Here we report that ASK1 proapoptotic activity is antagonized by association with 14-3-3 proteins. We found that ASK1 specifically bound 14-3-3 proteins via a site involving Ser-967 of ASK1. Interestingly, overexpression of 14-3-3 in HeLa cells blocked ASK1-induced apoptosis whereas disruption of the ASK1/14-3-3 interaction dramatically accelerated ASK1-induced cell death. Targeting of ASK1 by a 14-3-3-mediated survival pathway may provide a novel mechanism for the suppression of apoptosis.
引用
收藏
页码:8511 / 8515
页数:5
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