CREB is cleaved by caspases during neural cell apoptosis

被引:41
作者
François, F [1 ]
Godinho, MJ [1 ]
Grimes, ML [1 ]
机构
[1] Massey Univ, Inst Mol Biosci, Palmerston North, New Zealand
关键词
caspase; apoptosis; signal transduction; cAMP response element binding protein; neuroblastoma; in vitro reconstitution;
D O I
10.1016/S0014-5793(00)02316-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Programmed cell death, or apoptosis, is a tightly regulated process mediated by selective cleavage of proteins by caspases, resulting in ordered destruction of the cell. In addition to structural proteins, proteins that mediate anti-apoptotic signal transduction are also substrates; their destruction eliminates potential futile attempts to escape execution. We asked whether cAMP response element binding protein (CREB), a transcription factor that mediates nerve growth factor (NGF) survival signals, is a target for caspases during apoptosis. CREB was specifically cleaved by caspases in neuroblastoma extracts, and in cells induced to undergo apoptosis by staurosporine. The destruction of CREB eliminates a key factor that could reverse apoptosis. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:281 / 284
页数:4
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