4.8 Article

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

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0407686101

Keywords

DNA damage response; DNA replication

Funding

  1. NIGMS NIH HHS [GM322833, R01 GM024441, GM024441, R01 GM052948, GM52948] Funding Source: Medline

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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.

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