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SIRT6 is a DNA double-strand break sensor.

ABSTRACT: DNA double-strand breaks (DSB) are the most deleterious type of DNA damage. In this work, we show that SIRT6 directly recognizes DNA damage through a tunnel-like structure that has high affinity for DSB. SIRT6 relocates to sites of damage independently of signaling and known sensors. It activates downstream signaling for DSB repair by triggering ATM recruitment, H2AX phosphorylation and the recruitment of proteins of the homologous recombination and non-homologous end joining pathways. Our findings indicate that SIRT6 plays a previously uncharacterized role as a DNA damage sensor, a critical factor in initiating the DNA damage response (DDR). Moreover, other Sirtuins share some DSB-binding capacity and DDR activation. SIRT6 activates the DDR before the repair pathway is chosen, and prevents genomic instability. Our findings place SIRT6 as a sensor of DSB, and pave the road to dissecting the contributions of distinct DSB sensors in downstream signaling.

SUBMITTER: Onn L

PROVIDER: S-EPMC7051178 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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SIRT6 is a DNA double-strand break sensor.

Onn Lior L Portillo Miguel M Ilic Stefan S Cleitman Gal G Stein Daniel D Kaluski Shai S Shirat Ido I Slobodnik Zeev Z Einav Monica M Erdel Fabian F Akabayov Barak B Toiber Debra D

eLife 20200129

DNA double-strand breaks (DSB) are the most deleterious type of DNA damage. In this work, we show that SIRT6 directly recognizes DNA damage through a tunnel-like structure that has high affinity for DSB. SIRT6 relocates to sites of damage independently of signaling and known sensors. It activates downstream signaling for DSB repair by triggering ATM recruitment, H2AX phosphorylation and the recruitment of proteins of the homologous recombination and non-homologous end joining pathways. Our findi ...[more]

PMID: 31995034

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