There is growing evidence that the metabolic network is an integral regulator of cellular physiology. Dynamic changes in metabolite concentrations, metabolic flux, or network topology act as reporters of biological or environmental signals, and are required for the cell to trigger an appropriate biological reaction. Changes in the metabolic network are recognized by specific sensory macromolecules and translated into a transcriptional or translational response. The protein family of sirtuins, discovered more than 30 years ago as regulators of silent chromatin, seems to fulfill the role of a metabolic sensor during aging and conditions of caloric restriction. The archetypal sirtuin, yeast silent information regulator2 (SIR2), is an NAD+ dependent protein deacetylase that interacts with metabolic enzymes glyceraldehyde-3-phosphate dehydrogenase and alcohol dehydrogenase, as well as enzymes involved in NAD(H) synthesis, that provide or deprive NAD+ in its close proximity. This influences sirtuin activity, and facilitates a dynamic response of the metabolic network to changes in metabolism with effects on physiology and aging. The molecular network downstream Sir2, however, is complex. In just two orders, Sir2’s metabolism related interactions span half of the yeast proteome, and are connected with virtually every physiological process. Thus, although it is fundamental to analyze single molecular mechanisms, it is at the same time crucial to consider this genome-scale complexity when correlating single molecular events with complex phenotypes such as aging, cell growth, or stress resistance.
Keywords: sirtuins, metabolic network, glycolysis, caloric restriction, pentose phosphate pathway, aging, redox state, nicotinamide
Citation: Ralser M, Michel S and Breitenbach M (2012) Sirtuins as regulators of the yeast metabolic network. Front. Pharmacol. 3:32. doi: 10.3389/fphar.2012.00032
Received: 15 December 2011; Paper pending published: 13 January 2012;
Accepted: 17 February 2012; Published online: 08 March 2012.
Edited by:Aleksey G. Kazantsev, Harvard Medical School and Massachusetts General Hospital, USA
Reviewed by:Anthony A. Sauve, Weill Cornell Medical College, USA
Copyright: © 2012 Ralser, Michel and Breitenbach. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: Markus Ralser, Department of Biochemistry, Cambridge Systems Biology Centre, University of Cambridge, 80 Tennis Court Road, CB2 1GA Cambridge, UK. e-mail: firstname.lastname@example.org