The human Rad9-Rad1-Hus1 checkpoint complex stimulates flap endonuclease 1

被引:84
作者
Wang, WS
Brandt, P
Rossi, ML
Lindsey-Boltz, L
Podust, V
Fanning, E
Sancar, A
Bambara, RA [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Biochem & Biophys, Rochester, NY 14642 USA
[2] Vanderbilt Univ, Dept Biol Sci, Nashville, TN 37235 USA
[3] Univ N Carolina, Sch Med, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
关键词
DNA damage response; DNA replication;
D O I
10.1073/pnas.0407686101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The toroidal damage checkpoint complex Rad9-Rad1-Hus1 (9-1-1) has been characterized as a sensor of DNA damage. Flap endonuclease 1 (FEN1) is a structure-specific nuclease involved both in removing initiator RNA from Okazaki fragments and in DNA repair pathways. FEW activity is stimulated by proliferating cell nuclear antigen (PCNA), a toroidal sliding clamp that acts as a platform for DNA replication and repair complexes. We show that 9-1-1 also binds and stimulates FEN1. Stimulation is observed on a variety of flap, nick, and gapped substrates simulating repair intermediates. Blocking 9-1-1 entry to the double strands prevents a portion of the stimulation. Like PCNA stimulation, 9-1-1 stimulation cannot circumvent the tracking mechanism by which FEN1 enters the substrate; however, 9-1-1 does not substitute for PCNA in the stimulation of DNA polymerase delta. This suggests that 9-1-1 is a damage-specific activator of FEN1.
引用
收藏
页码:16762 / 16767
页数:6
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