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RETRACTED: Human SIRT6 Promotes DNA End Resection Through CtIP Deacetylation

2010; American Association for the Advancement of Science; Volume: 329; Issue: 5997 Linguagem: Inglês

10.1126/science.1192049

1095-9203

Abderrahmane Kaidi, Brian T. Weinert, Chunaram Choudhary, Stephen P. Jackson,

PARP inhibition in cancer therapy

SIRT6 belongs to the sirtuin family of protein lysine deacetylases, which regulate aging and genome stability. We found that human SIRT6 has a role in promoting DNA end resection, a crucial step in DNA double-strand break (DSB) repair by homologous recombination. SIRT6 depletion impaired the accumulation of replication protein A and single-stranded DNA at DNA damage sites, reduced rates of homologous recombination, and sensitized cells to DSB-inducing agents. We identified the DSB resection protein CtIP [C-terminal binding protein (CtBP) interacting protein] as a SIRT6 interaction partner and showed that SIRT6-dependent CtIP deacetylation promotes resection. A nonacetylatable CtIP mutant alleviated the effect of SIRT6 depletion on resection, thus identifying CtIP as a key substrate by which SIRT6 facilitates DSB processing and homologous recombination. These findings further clarify how SIRT6 promotes genome stability.