The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1

被引:367
作者
Delacroix, Sinny
Wagner, Jill M.
Kobayashi, Masahiko
Yamamoto, Ken-ichi
Karnitz, Larry M. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Radiat Oncol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Div Oncol Res, Rochester, MN 55905 USA
[4] Kanazawa Univ, Dept Mol Pathol, Kanazawa, Ishikawa 9200934, Japan
[5] Kanazawa Univ, Inst Canc Res, Kanazawa, Ishikawa 9200934, Japan
关键词
checkpoint; replication; Rad9; ATR; TopBP1; Chk1;
D O I
10.1101/gad.1547007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DNA replication stress triggers the activation of Checkpoint Kinase 1 (Chk1) in a pathway that requires the independent chromatin loading of the ATRIP-ATR (ATR-interacting protein/ATM [ataxia-telangiectasia mutated]-Rad3-related kinase) complex and the Rad9- Hus1-Rad1 (9-1-1) clamp. We show that Rad9' s role in Chk1 activation is to bind TopBP1, which stimulates ATR-mediated Chk1 phosphorylation via TopBP1' s activation domain ( AD), a domain that binds and activates ATR. Notably, fusion of the AD to proliferating cell nuclear antigen ( PCNA) or histone H2B bypasses the requirement for the 9-1-1 clamp, indicating that the 9-1-1 clamp's primary role in activating Chk1 is to localize the AD to a stalled replication fork.
引用
收藏
页码:1472 / 1477
页数:6
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