Chromatin and beyond: the multitasking roles for SIRT6

被引:294
作者
Kugel, Site [1 ]
Mostoslavsky, Raul [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Ctr Canc, Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
HISTONE DEACETYLASE SIRT6; SILENCING PROTEIN SIR2; STRAND BREAK REPAIR; DNA END RESECTION; LIFE-SPAN; SACCHAROMYCES-CEREVISIAE; HEPATIC GLUCONEOGENESIS; CALORIE RESTRICTION; GENOMIC INSTABILITY; SIR2-LIKE PROTEINS;
D O I
10.1016/j.tibs.2013.12.002
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
In recent years there has been a large expansion in our understanding of SIRT6 biology including its structure, regulation, biochemical activity, and biological roles. SIRT6 functions as an ADP-ribosylase and NAD(+)-dependent deacylase of both acetyl groups and long-chain fatty-acyl groups. Through these functions SIRT6 impacts upon cellular homeostasis by regulating DNA repair, telomere maintenance, and glucose and lipid metabolism, thus affecting diseases such diabetes, obesity, heart disease, and cancer. Such roles may contribute to the overall longevity and health of the organism. Until recently, the known functions of SIRT6 were largely restricted to the chromatin. In this article we seek to describe and expand this knowledge with recent advances in understanding the mechanisms of SIRT6 action and their implications for human biology and disease.
引用
收藏
页码:72 / 81
页数:10
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