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This version published online on April 24, 2007
Molecular Endocrinology, doi:10.1210/me.2007-0079
Molecular Endocrinology Vol. 0, No. 2007 200700791-
doi:10.1210/me.2007-0079
Copyright © 2007 by the Endocrine Society.
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*Cancer
*Degenerative Nerve Diseases

Submitted on February 12, 2007
Accepted on April 18, 2007

SIRTUIN FUNCTIONS IN HEALTH AND DISEASE

Hiroyasu Yamamoto, Kristina Schoonjans, and Johan Auwerx*

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CNRS / INSERM / ULP, 67404 Illkirch, France; Institut Clinique de la Souris, 67404 Illkirch, France

* To whom correspondence should be addressed. E-mail: auwerx{at}igbmc.u-strasbg.fr.

Sirtuins or Sir2-related enzymes have originally been defined as a family NAD+-dependent enzymes that deacetylate lysine residue on various proteins. Certain sirtuins have in addition an ADP-ribosyltransferase activity. The sirtuins are remarkably conserved throughout evolution from archaebacteria to eukaryotes. The mammalian sirtuins, SIRT1-7, are implicated in a variety of cellular functions ranging from gene silencing, over the control of the cell cycle and apoptosis, to energy homeostasis. On a whole body level, the wide range of cellular activities of the sirtuins suggest that they could constitute therapeutic targets to combat metabolic, neurodegenerative, and proliferative diseases. Here, we review some of the recent data related to the sirtuins and discuss their mode of action, their biological role in cellular and organismal models, and their possible association to age-related human diseases.


Key words: Sir2 • SIRT1-7 • Aging • Caloric restriction • Mitochondria • Metabolic diseases • Neurodegenerative diseases

NURSA Molecule Pages Link:

Nuclear Receptors:   PPARγ  |  HNF4α  |  AR
Coregulators:   PGC-1  |  Sirt1



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