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pubmed-article:20452416pubmed:abstractTextDietary restriction (DR) has been used for decades to retard aging in rodents, but its mechanism of action remains an enigma. A principal roadblock has been that DR affects many different processes, making it difficult to distinguish cause and effect. To address this problem, we applied a quantitative genetics approach utilizing the ILSXISS series of mouse recombinant inbred strains. Across 42 strains, mean female lifespan ranged from 380 to 1070days on DR (fed 60% of ad libitum [AL]) and from 490 to 1020days on an AL diet. Longevity under DR and AL is under genetic control, showing 34% and 36% heritability, respectively. There was no correlation between lifespans on DR and AL; thus different genes modulate longevity under the two regimens. DR lifespans are significantly correlated with female fertility after return to an AL diet after various periods of DR (R=0.44, P=0.006). We assessed fuel efficiency (FE, ability to maintain growth and body weight independent of absolute food intake) using a multivariate approach and found it to be correlated with longevity and female fertility, suggesting possible causality. We found several quantitative trait loci responsible for these traits, mapping to chromosomes 7, 9, and 15. We present a metabolic model in which the anti-aging effects of DR are consistent with the ability to efficiently utilize dietary resources.lld:pubmed
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pubmed-article:20452416pubmed:authorpubmed-author:NelsonJames...lld:pubmed
pubmed-article:20452416pubmed:authorpubmed-author:RikkeBrad ABAlld:pubmed
pubmed-article:20452416pubmed:authorpubmed-author:McQueenMatthe...lld:pubmed
pubmed-article:20452416pubmed:copyrightInfoCopyright 2010 Elsevier Inc. All rights reserved.lld:pubmed
pubmed-article:20452416pubmed:issnTypeElectroniclld:pubmed
pubmed-article:20452416pubmed:volume45lld:pubmed
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pubmed-article:20452416pubmed:pagination691-701lld:pubmed
pubmed-article:20452416pubmed:dateRevised2011-9-26lld:pubmed
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pubmed-article:20452416pubmed:articleTitleGenetic dissection of dietary restriction in mice supports the metabolic efficiency model of life extension.lld:pubmed
pubmed-article:20452416pubmed:affiliationInstitute for Behavioral Genetics, University of Colorado at Boulder, Boulder, CO 80309, USA. rikke@colorado.edulld:pubmed
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pubmed-article:20452416pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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