» Articles » PMID: 22408620

Sirtuins As Regulators of the Yeast Metabolic Network

Overview
Journal Front Pharmacol
Date 2012 Mar 13
PMID 22408620
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

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 silentinformationregulator2 (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.

Citing Articles

Novel Approach to Skin Anti-Aging: Boosting Pharmacological Effects of Exogenous Nicotinamide Adenine Dinucleotide (NAD) by Synergistic Inhibition of CD38 Expression.

Kang S, Park J, Cheng Z, Ye S, Jun S, Kang N Cells. 2024; 13(21.

PMID: 39513906 PMC: 11544843. DOI: 10.3390/cells13211799.


An epigenetic change in a moth is generated by temperature and transmitted to many subsequent generations mediated by RNA.

Pavelka J, Polakova S, Pavelkova V, Galeta P PLoS One. 2024; 19(3):e0292179.

PMID: 38451888 PMC: 10919628. DOI: 10.1371/journal.pone.0292179.


Insights into the Conserved Regulatory Mechanisms of Human and Yeast Aging.

Dahiya R, Mohammad T, Alajmi M, Rehman M, Hasan G, Hussain A Biomolecules. 2020; 10(6).

PMID: 32526825 PMC: 7355435. DOI: 10.3390/biom10060882.


Involvement of miR-Let7A in inflammatory response and cell survival/apoptosis regulated by resveratrol in THP-1 macrophage.

Song J, Jun M, Ahn M, Kim O Nutr Res Pract. 2016; 10(4):377-84.

PMID: 27478543 PMC: 4958639. DOI: 10.4162/nrp.2016.10.4.377.


Yeast sirtuins and the regulation of aging.

Wierman M, Smith J FEMS Yeast Res. 2013; 14(1):73-88.

PMID: 24164855 PMC: 4365911. DOI: 10.1111/1567-1364.12115.


References
1.
Smith Jr D, McClure J, Matecic M, Smith J . Calorie restriction extends the chronological lifespan of Saccharomyces cerevisiae independently of the Sirtuins. Aging Cell. 2007; 6(5):649-62. DOI: 10.1111/j.1474-9726.2007.00326.x. View

2.
Postma L, Lehrach H, Ralser M . Surviving in the cold: yeast mutants with extended hibernating lifespan are oxidant sensitive. Aging (Albany NY). 2010; 1(11):957-60. PMC: 2815748. DOI: 10.18632/aging.100104. View

3.
Kustatscher G, Hothorn M, Pugieux C, Scheffzek K, Ladurner A . Splicing regulates NAD metabolite binding to histone macroH2A. Nat Struct Mol Biol. 2005; 12(7):624-5. DOI: 10.1038/nsmb956. View

4.
Fritze C, Verschueren K, Strich R, Easton Esposito R . Direct evidence for SIR2 modulation of chromatin structure in yeast rDNA. EMBO J. 1997; 16(21):6495-509. PMC: 1170255. DOI: 10.1093/emboj/16.21.6495. View

5.
Kennedy B, Austriaco Jr N, Zhang J, Guarente L . Mutation in the silencing gene SIR4 can delay aging in S. cerevisiae. Cell. 1995; 80(3):485-96. DOI: 10.1016/0092-8674(95)90499-9. View