A cytosolic NAD-dependent deacetylase, Hst2p, can modulate nucleolar and telomeric silencing in yeast

被引:130
作者
Perrod, S [1 ]
Cockell, MM [1 ]
Laroche, T [1 ]
Renauld, H [1 ]
Ducrest, AL [1 ]
Bonnard, C [1 ]
Gasser, SM [1 ]
机构
[1] Swiss Inst Expt Canc Res, CH-1066 Epalinges, Switzerland
关键词
homologues of Sir2p; nucleolus; SIR2; telomeric silencing; yeast;
D O I
10.1093/emboj/20.1.197
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 budding yeast, the silent information regulator Sir2p is a nuclear NAD-dependent deacetylase that is essential for both telomeric and rDNA silencing. All eukaryotic species examined to date have multiple homologues of Sir two (HSTs), which share a highly conserved globular core domain. Here we report that yeast Hst2p and a mammalian Hst2p homologue, hSirT2p, are cytoplasmic in yeast and human cells, in contrast to yHst1p and ySir2p which are exclusively nuclear. Although yHst2p cannot restore silencing in a sir2 deletion, overexpression of yHst2p influences nuclear silencing events in a SIR2 strain, derepressing subtelomeric silencing while increasing repression in the rDNA. In contrast, a form of ySir2p carrying a point mutation in the conserved core domain disrupts both telomeric position effect (TPE) and rDNA repression at low expression levels, This argues that nonnuclear yHst2p can compete for a substrate or ligand specifically required for telomeric, and not rDNA repression.
引用
收藏
页码:197 / 209
页数:13
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