Abstract
Calorie restriction extends life-span in a wide variety of organisms. Although it has been suggested that calorie restriction may work by reducing the levels of reactive oxygen species produced during respiration, the mechanism by which this regimen slows aging is uncertain. Here, we mimicked calorie restriction in yeast by physiological or genetic means and showed a substantial extension in life-span. This extension was not observed in strains mutant for SIR2 (which encodes the silencing protein Sir2p) or NPT1 (a gene in a pathway in the synthesis of NAD, the oxidized form of nicotinamide adenine dinucleotide). These findings suggest that the increased longevity induced by calorie restriction requires the activation of Sir2p by NAD.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Cyclic AMP-Dependent Protein Kinases / metabolism
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DNA, Circular / genetics
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DNA, Circular / metabolism
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DNA, Fungal / genetics
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DNA, Fungal / metabolism
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DNA, Ribosomal / genetics
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DNA, Ribosomal / metabolism
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Energy Intake*
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Enzyme Activation
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Gene Silencing*
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Glucose / metabolism*
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Histone Deacetylases / genetics
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Histone Deacetylases / metabolism*
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Longevity*
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Mutation
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NAD / metabolism*
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Pentosyltransferases / genetics
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Pentosyltransferases / metabolism
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Recombination, Genetic
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism
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Saccharomyces cerevisiae / physiology*
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Silent Information Regulator Proteins, Saccharomyces cerevisiae*
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Sirtuin 2
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Sirtuins
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Trans-Activators / genetics
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Trans-Activators / metabolism*
Substances
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DNA, Circular
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DNA, Fungal
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DNA, Ribosomal
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Silent Information Regulator Proteins, Saccharomyces cerevisiae
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Trans-Activators
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NAD
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Pentosyltransferases
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Cyclic AMP-Dependent Protein Kinases
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SIR2 protein, S cerevisiae
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Sirtuin 2
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Sirtuins
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Histone Deacetylases
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nicotinate phosphoribosyltransferase
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Glucose