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SIRT6 protein deacetylase interacts with MYH DNA glycosylase, APE1 endonuclease, and Rad9-Rad1-Hus1 checkpoint clamp.

BMC molecular biology | 2015

SIRT6, a member of the NAD(+)-dependent histone/protein deacetylase family, regulates genomic stability, metabolism, and lifespan. MYH glycosylase and APE1 are two base excision repair (BER) enzymes involved in mutation avoidance from oxidative DNA damage. Rad9-Rad1-Hus1 (9-1-1) checkpoint clamp promotes cell cycle checkpoint signaling and DNA repair. BER is coordinated with the checkpoint machinery and requires chromatin remodeling for efficient repair. SIRT6 is involved in DNA double-strand break repair and has been implicated in BER. Here we investigate the direct physical and functional interactions between SIRT6 and BER enzymes.

Pubmed ID: 26063178 RIS Download

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Associated grants

  • Agency: NIH HHS, United States
    Id: S10 OD011969
  • Agency: NIH HHS, United States
    Id: S10-OD011969
  • Agency: NCI NIH HHS, United States
    Id: R01 CA078391
  • Agency: NIA NIH HHS, United States
    Id: R21-AG045545
  • Agency: NCI NIH HHS, United States
    Id: R01-CA78391
  • Agency: NIA NIH HHS, United States
    Id: R21 AG045545

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