Dicer interacts with SIRT7 and regulates H3K18 deacetylation in response to DNA damaging agents

Pei-Ying Zhang(Wenzhou Medical University), Guiling Li(Wenzhou Medical University), Zhujun Deng(Wenzhou Medical University), Liyuan Liu(Wenzhou Medical University), Li Chen(Wenzhou Medical University), Junzhou Tang(Army Medical University), Yu-Qun Wang(Wenzhou Medical University), Su-Ting Cao(Wenzhou Medical University), Yu‐Xiao Fang(Wenzhou Medical University), Fuping Wen(Wenzhou Medical University), Yunsheng Xu(Wenzhou Medical University), Xiaoming Chen(Wenzhou Medical University), Keqing Shi(Wenzhou Medical University), Wenfeng Li(Wenzhou Medical University), Congying Xie(Wenzhou Medical University), Kai‐Fu Tang(Wenzhou Medical University)
Nucleic Acids Research
December 23, 2015
Cited by 68Open Access
Full Text

Abstract

Dicer participates in heterochromatin formation in fission yeast and plants. However, whether it has a similar role in mammals remains controversial. Here we showed that the human Dicer protein interacts with SIRT7, an NAD(+)-dependent H3K18Ac (acetylated lysine 18 of histone H3) deacetylase, and holds a proportion of SIRT7 in the cytoplasm. Dicer knockdown led to an increase of chromatin-associated SIRT7 and simultaneously a decrease of cytoplasmic SIRT7, while its overexpression induced SIRT7 reduction in the chromatin-associated fraction and increment in the cytoplasm. Furthermore, DNA damaging agents promoted Dicer expression, leading to decreased level of chromatin-associated SIRT7 and increased level of H3K18Ac, which can be alleviated by Dicer knockdown. Taken together with that H3K18Ac was exclusively associated with the chromatin, our findings suggest that Dicer induction by DNA damaging treatments prevents H3K18Ac deacetylation, probably by trapping more SIRT7 in the cytoplasm.


Related Papers

No related papers found

Powered by citation graph analysis