Mitochondrial sirtuins

被引:197
作者
Huang, Jing-Yi [1 ]
Hirschey, Matthew D. [1 ]
Shimazu, Tadahiro [1 ]
Ho, Linh [1 ]
Verdin, Eric [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2010年 / 1804卷 / 08期
关键词
Mitochondria; Sirtuin; SIRT3; SIRT4; SIRT5; O-Acetyl-ADP-ribose; Acetylation; ACETYL-ADP-RIBOSE; INSULIN DEGRADING ENZYME; COLONY-ENHANCING FACTOR; RAT-LIVER MITOCHONDRIA; COA SYNTHETASE 2; YEAST SIR2 GENE; GLUTAMATE-DEHYDROGENASE; CALORIE RESTRICTION; LYSINE ACETYLATION; DEPENDENT DEACETYLASE;
D O I
10.1016/j.bbapap.2009.12.021
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
Sirtuins have emerged as important proteins in aging, stress resistance and metabolic regulation. Three sirtuins, SIRT3, 4 and 5, are located within the mitochondrial matrix. SIRT3 and SIRT5 are NAD(+)-dependent deacetylases that remove acetyl groups from acetyllysine-modified proteins and yield 2'-O-acetyl-ADP-ribose and nicotinamide. SIRT4 can transfer the ADP-ribose group from NAD(+) onto acceptor proteins. Recent findings reveal that a large fraction of mitochondrial proteins are acetylated and that mitochondrial protein acetylation is modulated by nutritional status. This and the identification of targets for SIRT3, 4 and 5 support the model that mitochondrial sirtuins are metabolic sensors that modulate the activity of metabolic enzymes via protein deacetylation or mono-ADP-ribosylation. Here, we review and discuss recent progress in the study of mitochondrial sirtuins and their targets. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1645 / 1651
页数:7
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