4.8 Review

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

期刊

ONCOGENE
卷 28, 期 33, 页码 2925-2939

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2009.170

关键词

cell cycle; cyclin; Cdk; DNA damage; meiosis; knockout mouse

资金

  1. A*STAR of Singapore (PK)
  2. NIH
  3. National Cancer Institute
  4. Center for Cancer Research

向作者/读者索取更多资源

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

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据