Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms

被引:596
作者
Satyanarayana, A. [2 ]
Kaldis, P. [1 ]
机构
[1] IMCB, Lab Cell Div & Canc, Singapore 138673, Singapore
[2] NCI, Mouse Canc Genet Program, Ctr Canc Res, Frederick, MD 21702 USA
关键词
cell cycle; cyclin; Cdk; DNA damage; meiosis; knockout mouse; RNA-POLYMERASE-II; DEPENDENT KINASES; PROTEIN-KINASE; ACTIVATING KINASE; S-PHASE; RETINOBLASTOMA PROTEIN; EMBRYONIC LETHALITY; IN-VIVO; SUBCELLULAR-LOCALIZATION; CENTROSOME DUPLICATION;
D O I
10.1038/onc.2009.170
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
After a decade of extensive work on gene knockout mouse models of cell-cycle regulators, the classical model of cell-cycle regulation was seriously challenged. Several unexpected compensatory mechanisms were uncovered among cyclins and Cdks in these studies. The most astonishing observation is that Cdk2 is dispensable for the regulation of the mitotic cell cycle with both Cdk4 and Cdk1 covering for Cdk2's functions. Similar to yeast, it was recently discovered that Cdk1 alone can drive the mammalian cell cycle, indicating that the regulation of the mammalian cell cycle is highly conserved. Nevertheless, cell-cycle-independent functions of Cdks and cyclins such as in DNA damage repair are still under investigation. Here we review the compensatory mechanisms among major cyclins and Cdks in mammalian cell-cycle regulation. Oncogene (2009) 28, 2925-2939; doi:10.1038/onc.2009.170; published online 29 June 2009
引用
收藏
页码:2925 / 2939
页数:15
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