SIRT7: a sentinel of genome stability

被引:33
|
作者
Tang, Ming [1 ]
Tang, Huangqi [2 ]
Tu, Bo [3 ]
Zhu, Wei-Guo [2 ]
机构
[1] Tongji Univ Sch Med, Shanghai First Matern & Infant Hosp, Clin & Translat Res Ctr, Shanghai Key Lab Maternal Fetal Med, Shanghai 201204, Peoples R China
[2] Shenzhen Univ Sch Med, Shenzhen Univ Int Canc Ctr, Dept Biochem & Mol Biol, Guangdong Key Lab Genome Instabil & Human Dis Pr, Shenzhen 518055, Peoples R China
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98101 USA
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
SIRT7; genome stability; DNA repair; ageing; cancer; DNA-DAMAGE RESPONSE; RNA-POLYMERASE-I; SIRT7-DEPENDENT DEACETYLATION; REPAIR; STRESS; ACTIVATION; CANCER; ATM; SIRTUINS; AUTOPHOSPHORYLATION;
D O I
10.1098/rsob.210047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SIRT7 is a class III histone deacetylase that belongs to the sirtuin family. The past two decades have seen numerous breakthroughs in terms of understanding SIRT7 biological function. We now know that this enzyme is involved in diverse cellular processes, ranging from gene regulation to genome stability, ageing and tumorigenesis. Genomic instability is one hallmark of cancer and ageing; it occurs as a result of excessive DNA damage. To counteract such instability, cells have evolved a sophisticated regulated DNA damage response mechanism that restores normal gene function. SIRT7 seems to have a critical role in this response, and it is recruited to sites of DNA damage where it recruits downstream repair factors and directs chromatin regulation. In this review, we provide an overview of the role of SIRT7 in DNA repair and maintaining genome stability. We pay particular attention to the implications of SIRT7 function in cancer and ageing.
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页数:8
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