Regulation of cyclin-Cdk activity in mammalian cells

被引:348
作者
Obaya, AJ [1 ]
Sedivy, JM
机构
[1] Univ Oviedo, Fac Med, Inst Oncol, IUOPA,Area Fisiol, Oviedo 33006, Spain
[2] Brown Univ, Div Biol & Med, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
关键词
cell cycle; cyclin; cdk; cdk inhibitor; cdk phosphorylation; Rb phosphorylation; E2F/Rb restriction point; ubiquitin-proteasome pathway; cellular localization;
D O I
10.1007/s00018-002-8410-1
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
Cell cycle progression is driven by the coordinated regulation of the activities of cyclin-dependent kinases (Cdks). Of the several mechanisms known to regulate Cdk activity in response to external signals, regulation of cyclin gene expression, post-translational modification of Cdks by phosphorylation-dephosphorylation cascades, and the interaction of cyclin/Cdk complexes with protein inhibitors have been thoroughly studied. During recent years, much attention has also been given to mechanisms that regulate protein degradation by the ubiquitin/proteasome pathway, as well as to the regulation of subcellular localization of the proteins that comprise the intrinsic cell cycle clock. The purpose of the present review is to summarize the most important aspects of the various mechanisms implicated in cell cycle regulation.
引用
收藏
页码:126 / 142
页数:17
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