Mitotic crisis The unmasking of a novel role for RPA

被引:24
作者
Anantha, Rachel William
Borowiec, James A. [1 ]
机构
[1] NYU, Sch Med, Dept Biochem, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
RPA; Plk1; centrosome; mitotic DNA damage; spindle assembly checkpoint; phosphorylation; DNA-DAMAGE CHECKPOINT; TOUSLED-LIKE KINASE; CHROMATIN ASSEMBLY FACTORS; POLO-LIKE KINASE-1; CHROMOSOME SEGREGATION; CELL-CYCLE; PROTEIN-KINASES; PLK1; SUBSTRATE; PHOSPHORYLATION; REPLICATION;
D O I
10.4161/cc.8.3.7496
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Mitotic DNA damage is a constant threat to genomic integrity, yet understanding of the cellular responses to this stress remain incomplete. Recent work by Anantha et al. (2008; PNAS 105: 12903-8) has found surprising evidence that RPA, the primary eukaryotic single-stranded DNA-binding protein, can stimulate the ability of cells to exit mitosis into a 2N G(1) phase. Along with providing additional discussion of this study, we review evidence suggesting that DNA replication and repair factors can modulate mitotic transit by acting through Polo-like kinase-1 (Plk1) and the centrosome. 'A crisis unmasks everyone.'-Mason Cooley, U. S. aphorist.
引用
收藏
页码:357 / 361
页数:5
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