Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Trends Biochem Sci. 2011 Jan;36(1):39-46. doi: 10.1016/j.tibs.2010.07.009. Epub 2010 Aug 21.
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.
酿酒酵母 Sir2 是一种依赖 NAD(+)的组蛋白去乙酰化酶,它将染色质沉默与基因组稳定性、细胞代谢和寿命调节联系起来。在小鼠中,Sir2 家族成员 SIRT6 的缺乏会导致基因组不稳定、代谢缺陷和与衰老相关的退行性病变。直到最近,SIRT6 还是一种孤儿酶,其催化活性和底物尚不清楚。然而,新的机制见解来自于发现 SIRT6 是一种高度底物特异性的组蛋白去乙酰化酶,它在几种生理环境中促进适当的染色质功能,包括端粒和基因组稳定、基因表达和 DNA 修复。通过维持哺乳动物基因组的完整性和表达,SIRT6 因此在几个方面发挥作用,与 Sir2 的功能平行。在本文中,我们综述了对 SIRT6 作用机制的理解的最新进展及其对人类生物学和疾病的影响。