SIRT1 and SIRT3 deacetylate homologous substrates: AceCS1,2 and HMGCS1,2

被引:83
|
作者
Hirschey, Matthew D. [1 ]
Shimazu, Tadahiro [1 ]
Capra, John A. [2 ]
Pollard, Katherine S. [2 ,3 ,4 ]
Verdin, Eric [1 ,5 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Gladstone Inst Cardiovasc Dis, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Div Biostat, San Francisco, CA 94107 USA
[4] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94107 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
来源
AGING-US | 2011年 / 3卷 / 06期
关键词
sirtuins; evolution; deacetylases; aging; ELEMENT-BINDING PROTEINS; ACETYL-COA SYNTHETASE; CALORIE RESTRICTION; LYSINE ACETYLATION; LIFE-SPAN; GENE; LONGEVITY; EVOLUTION; OXIDATION; PATHWAY;
D O I
10.18632/aging.100339
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
SIRT1 and SIRT3 are NAD+-dependent protein deacetylases that are evolutionarily conserved across mammals. These proteins are located in the cytoplasm/nucleus and mitochondria, respectively. Previous reports demonstrated that human SIRT1 deacetylates Acetyl-CoA Synthase 1 (AceCS1) in the cytoplasm, whereas SIRT3 deacetylates the homologous Acetyl-CoA Synthase 2 (AceCS2) in the mitochondria. We recently showed that 3-hydroxy-3-methylglutaryl CoA synthase 2 (HMGCS2) is deacetylated by SIRT3 in mitochondria, and we demonstrate here that SIRT1 deacetylates the homologous 3-hydroxy-3-methylglutaryl CoA synthase 1 (HMGCS1) in the cytoplasm. This novel pattern of substrate homology between cytoplasmic SIRT1 and mitochondrial SIRT3 suggests that considering evolutionary relationships between the sirtuins and their substrates may help to identify and understand the functions and interactions of this gene family. In this perspective, we take a first step by characterizing the evolutionary history of the sirtuins and these substrate families.
引用
收藏
页码:635 / 642
页数:8
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