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Regulation of cell cycle checkpoints by polo-like kinases
被引:91
|作者:
Xie, SQ
Xie, B
Lee, MY
Dai, W
[1
]
机构:
[1] New York Med Coll, Dept Med, Mol Carcinogenesis Div, Valhalla, NY 10595 USA
[2] New York Med Coll, Brander Canc Res Inst, Valhalla, NY 10595 USA
[3] New York Med Coll, Dept Biochem, Mol Carcinogenesis Div, Valhalla, NY 10595 USA
来源:
关键词:
polo;
polo-like kinases;
cell cycle;
checkpoint;
cell division;
D O I:
10.1038/sj.onc.1208218
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:
Protein kinases play a pivotal role in execution of cell division. Polo and Polo-like kinases have emerged as major regulators for various cell cycle checkpoints. Early genetic studies have demonstrated that CDC5, a budding yeast counterpart of vertebrate Plks, is essential for successful mitotic progression. Mammalian Plks localize primarily to the centrosome during interphase and the mitotic apparatus during mitosis. Many key cell cycle regulators such as p53, Cdc25C, cyclin B, components of the anaphase-promoting complex, and mitotic motor proteins are directly targeted by Plks. Although the exact mechanism of action of these protein kinases in vivo remains to be elucidated, Plks are important mediators for various cell cycle checkpoints that monitor centrosome duplication, DNA replication, formation of bipolar mitotic spindle, segregation of chromosomes, and mitotic exit, thus protecting cells against genetic instability during cell division.
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页码:277 / 286
页数:10
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