Chk1-dependent regulation of Cdc25B functions to coordinate mitotic events

被引:43
作者
Loeffler, Harald
Rebacz, Blanka
Ho, Anthony D.
Lukas, Jiri
Bartek, Jiri
Kraemer, Alwin
机构
[1] Univ Heidelberg, German Canc Res Ctr, DKFZ, Clin Cooperat Unit Mol Hematol Oncol, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Internal Med 5, D-69120 Heidelberg, Germany
[3] Danish Canc Soc, Inst Canc Biol, Copenhagen, Denmark
[4] Danish Canc Soc, Ctr Genotox Stress Res, Copenhagen, Denmark
关键词
G(2)/M transition; mitosis; cell cycle checkpoints; DNA damage response; Chk1; Cdc25A; Cdc25B;
D O I
10.4161/cc.5.21.3435
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The coordination of mitotic spindle formation and chromatin condensation is an essential prerequisite for successful mitosis. Both events are thought to be initiated by cyclin B/Cdk1, whose initial activation occurs in late prophase at the centrosomes. Recently, we have shown that Chk1 localizes to interphase centrosomes and thereby negatively regulates entry into mitosis by preventing premature activation of cyclin B/Cdk1. Here, we demonstrate that inhibition of Chk1 kinase induces mitotic entry with regular spindle assembly but aberrant and mislocalized chromatin. This effect, which we have termed the 'paraspindle' phenotype, was reverted by downregulation of Cdc25B phosphatase using siRNA, which restored normal mitosis with regular chromatin. Analogous to Chk1 inhibition, the 'paraspindle' phenotype was induced by overexpression of Cdc25B but not Cdc25A. Our results suggest that Chk1 functions to coordinate mitotic events through regulation of Cdc25B.
引用
收藏
页码:2543 / 2547
页数:5
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