Ontology highlight
ABSTRACT:
SUBMITTER: Li L
PROVIDER: S-EPMC4961794 | biostudies-literature | 2016 Jul
REPOSITORIES: biostudies-literature
Li Lei L Shi Lan L Yang Shangda S Yan Ruorong R Zhang Di D Yang Jianguo J He Lin L Li Wanjin W Yi Xia X Sun Luyang L Liang Jing J Cheng Zhongyi Z Shi Lei L Shang Yongfeng Y Yu Wenhua W
Nature communications 20160720
Although SIRT7 is a member of sirtuin family proteins that are described as NAD(+)-dependent class III histone deacetylases, the intrinsic enzymatic activity of this sirtuin protein remains to be investigated and the cellular function of SIRT7 remains to be explored. Here we report that SIRT7 is an NAD(+)-dependent histone desuccinylase. We show that SIRT7 is recruited to DNA double-strand breaks (DSBs) in a PARP1-dependent manner and catalyses desuccinylation of H3K122 therein, thereby promotin ...[more]