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PMID: 20060508 Published · ppublish English Journal Article Review

Mitochondrial sirtuins.

Biochimica et biophysica acta ·Vol. 1804 ·No. 8 ·2010-08-00 ·Pages 1645-51

Huang JY, Hirschey MD, Shimazu T, Ho L, Verdin E

Abstract

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.

MeSH Terms
Acetylation Animals Group III Histone Deacetylases/metabolism Humans Mice Mitochondria/metabolism Mitochondrial Proteins/metabolism Models, Biological NAD/metabolism O-Acetyl-ADP-Ribose/metabolism Sirtuin 3/metabolism Sirtuins/metabolism
Chemicals
Mitochondrial Proteins O-Acetyl-ADP-Ribose NAD Group III Histone Deacetylases Sirtuin 3 Sirtuins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Huang Jing-Yi
Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA, USA.
Hirschey Matthew D
Shimazu Tadahiro
Ho Linh
Verdin Eric
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2010-08-00
Epub
2010-00-07
Pages
1645-51
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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