Chromatin regulation and genome maintenance by mammalian SIRT6

被引:120
|
作者
Tennen, Ruth I. [1 ,2 ]
Chua, Katrin F. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Canc Biol Program, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Palo Alto, CA 94304 USA
基金
美国国家科学基金会;
关键词
SILENCING PROTEIN SIR2; LIFE-SPAN EXTENSION; NF-KAPPA-B; SACCHAROMYCES-CEREVISIAE; HISTONE H3; CALORIE RESTRICTION; ADP-RIBOSYLTRANSFERASE; DEACETYLASE ACTIVITY; SIR2-LIKE PROTEINS; RIBOSOMAL DNA;
D O I
10.1016/j.tibs.2010.07.009
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
Saccharomyces cerevisiae Sir2 is an NAD(+)-dependent histone deacetylase that links chromatin silencing to genomic stability, cellular metabolism and lifespan regulation. In mice, deficiency for the Sir2 family member SIRT6 leads to genomic instability, metabolic defects and degenerative pathologies associated with aging. Until recently, SIRT6 was an orphan enzyme whose catalytic activity and substrates were unclear. However, new mechanistic insights have come from the discovery that SIRT6 is a highly substrate-specific histone deacetylase that promotes proper chromatin function in several physiologic contexts, including telomere and genome stabilization, gene expression and DNA repair. By maintaining both the integrity and the expression of the mammalian genome, SIRT6 thus serves several roles that parallel Sir2 function. In this article, we review recent advances in understanding the mechanisms of SIRT6 action and their implications for human biology and disease.
引用
收藏
页码:39 / 46
页数:8
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