14-3-3 proteins as signaling integration points for cell cycle control and apoptosis

被引:246
作者
Gardino, Alexandra K. [1 ,2 ]
Yaffe, Michael B. [1 ,2 ]
机构
[1] MIT, Dept Biol, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
关键词
14-3-3; DNA damage; Cell cycle checkpoint; Apoptosis; Signal transduction; Mitosis; DNA-DAMAGE RESPONSE; POLO-LIKE KINASE-1; S-PHASE; BETA-TRCP; NUCLEAR EXPORT; PHOSPHORYLATION SITES; DEPENDENT DEGRADATION; CDC25; PHOSPHATASES; CHECKPOINT CONTROL; SURVIVAL SIGNALS;
D O I
10.1016/j.semcdb.2011.09.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
14-3-3 proteins play critical roles in the regulation of cell fate through phospho-dependent binding to a large number of intracellular proteins that are targeted by various classes of protein kinases. 14-3-3 proteins play particularly important roles in coordinating progression of cells through the cell cycle, regulating their response to DNA damage, and influencing life-death decisions following internal injury or external cytokine-mediated cues. This review focuses on 14-3-3-dependent pathways that control cell cycle arrest and recovery, and the influence of 14-3-3 on the apoptotic machinery at multiple levels of regulation. Recognition of 14-3-3 proteins as signaling integrators that connect protein kinase signaling pathways to resulting cellular phenotypes, and their exquisite control through feedforward and feedback loops, identifies new drug targets for human disease, and highlights the emerging importance of using systems-based approaches to understand signal transduction events at the network biology level. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:688 / 695
页数:8
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