Evidence that DNA damage detection machinery participates in DNA repair

被引:69
作者
Helt, CE
Wang, WS
Keng, PC
Bambara, RA [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Biophys & Biochem, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Radiat Oncol, Rochester, NY 14642 USA
关键词
DNA damage; cell cycle checkpoints; DNA replication; DNA repair;
D O I
10.4161/cc.4.4.1598
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The toroidal Rad9-Rad1-Hus1 checkpoint complex (9-1-1) is structurally similar to the proliferating cell nuclear antigen ( PCNA), which serves as a sliding clamp platform for DNA replication and repair. 9-1-1 has been characterized as a sensor of DNA damage that functions in concert with the checkpoint control proteins ATM and ATR. However, recent data suggest that the 9-1-1 complex and its individual Rad9 component serve different and multiple functions in cells by sensing DNA damage, stimulating apoptosis, and regulating gene transcription. Recently it was reported that 9-1-1 interacts with and/or stimulates components of the base excision repair (BER) pathway including the S. pombe MutY homolog (MYH), human polymerase beta (Pol beta), and flap endonuclease 1 ( FEN1). Furthermore, preliminary results indicate a stimulation of DNA ligase I. In this review, the likely direct participation of 9-1-1 in DNA repair is discussed.
引用
收藏
页码:529 / 532
页数:4
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