Cut5 is required for the binding of Atr and DNA polymerase α to genotoxin-damaged chromatin

被引:52
作者
Parrilla-Castellar, E
Karnitz, LM
机构
[1] Mayo Clin & Mayo Fdn, Div Dev Oncol Res, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Mayo Grad Sch, Tumor Biol Program, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Mayo Grad Sch, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Div Radiat Oncol, Rochester, MN 55905 USA
关键词
D O I
10.1074/jbc.C300418200
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
DNA damage triggers the assembly of checkpoint signaling proteins on chromatin that activate the Chk1 signaling pathway and block S-phase progression. Here we show that genotoxin-induced Chk1 activation requires Cut5 (Mus101/TopBP1) in a process that is independent of the role of Cut5 in DNA replication. Analysis of the role of Cut5 in checkpoint activation revealed that it associated with chromatin following DNA damage in a process that required RPA. Additionally, Cut5 was required for the recruitment of Atr, DNA polymerase alpha, and Rad1 but not RPA to chromatin following DNA damage. Taken together, these results demonstrate that Cut5 plays an integral role in the recruitment and assembly of the Chk1 signaling cascade components following DNA damage.
引用
收藏
页码:45507 / 45511
页数:5
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