SIRT6 is required for maintenance of telomere position effect in human cells

被引:108
作者
Tennen, Ruth I. [1 ,2 ]
Bua, Dennis J. [3 ]
Wright, Woodring E. [4 ]
Chua, Katrin F. [1 ,2 ,5 ]
机构
[1] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Canc Biol Program, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
[5] VA Palo Alto Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Palo Alto, CA 94304 USA
来源
NATURE COMMUNICATIONS | 2011年 / 2卷
基金
美国国家科学基金会;
关键词
SACCHAROMYCES-CEREVISIAE; HISTONE H3; GENOMIC STABILITY; GENE-EXPRESSION; LIFE-SPAN; CHROMATIN; DEACETYLATION; YEAST; HETEROCHROMATIN; MODIFIERS;
D O I
10.1038/ncomms1443
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Saccharomyces cerevisiae, the repressive chromatin environment at telomeres gives rise to telomere position effect (TPE), the epigenetic silencing of telomere-proximal genes. Chromatin-modifying factors that control TPE in yeast have been extensively studied, and, among these, the lifespan regulator and silencing protein Sir2 has a pivotal role. In contrast, the factors that generate and maintain silent telomeric chromatin in human cells remain largely unknown. Here we show that the Sir2 family member SIRT6 is required for maintenance of TPE in human cells. RNAi-mediated depletion of SIRT6 abrogates silencing of both an integrated telomeric transgene and an endogenous telomere-proximal gene. Moreover, enhanced telomeric silencing in response to telomere elongation is associated with increased repressive chromatin marks, and this heterochromatic milieu is lost in SIRT6-deficient cells. Together, these findings establish a new role for SIRT6 in regulating an ageing-associated epigenetic silencing process and provide new mechanistic insight into chromatin silencing at telomeres.
引用
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页数:7
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