Wang Wensheng, Brandt Patrick, Rossi Marie L, Lindsey-Boltz Laura, Podust Vladimir, Fanning Ellen, Sancar Aziz, Bambara Robert A
Department of Biochemistry and Biophysics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16762-7. doi: 10.1073/pnas.0407686101. Epub 2004 Nov 19.
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. FEN1 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 beta. This suggests that 9-1-1 is a damage-specific activator of FEN1.
环形损伤检查点复合物Rad9-Rad1-Hus1(9-1-1)已被确定为DNA损伤的传感器。瓣状核酸内切酶1(FEN1)是一种结构特异性核酸酶,既参与从冈崎片段中去除引发RNA,也参与DNA修复途径。FEN1的活性受到增殖细胞核抗原(PCNA)的刺激,PCNA是一种环形滑动夹,作为DNA复制和修复复合物的平台。我们发现9-1-1也能结合并刺激FEN1。在模拟修复中间体的各种瓣状、切口和缺口底物上都观察到了刺激作用。阻止9-1-1进入双链会阻止部分刺激作用。与PCNA刺激一样,9-1-1刺激不能绕过FEN1进入底物的追踪机制;然而,9-1-1在刺激DNA聚合酶β时不能替代PCNA。这表明9-1-1是FEN1的损伤特异性激活剂。