Abstract

Dietary restriction extends life span in diverse species including Caenorhabditis elegans. However, the downstream cellular targets regulated by dietary restriction are largely unknown. Autophagy, an evolutionary conserved lysosomal degradation pathway, is induced under starvation conditions and regulates life span in insulin signaling C. elegans mutants. We now report that two essential autophagy genes (bec-1 and Ce-atg7) are required for the longevity phenotype of the C. elegans dietary restriction mutant (eat-2(ad1113) animals. Thus, we propose that autophagy mediates the effect, not only of insulin signaling, but also of dietary restriction on the regulation of C. elegans life span. Since autophagy and longevity control are highly conserved from C. elegans to mammals, a similar role for autophagy in dietary restriction-mediated life span extension may also exist in mammals.

Keywords

BiologyCaenorhabditis elegansAutophagyLongevityPhenotypeCell biologyMutantGeneticsStarvationTOR signalingModel organismCaenorhabditisLife spanGeneSignal transductionEvolutionary biologyEndocrinologyApoptosis

MeSH Terms

AnimalsAutophagyCaenorhabditis elegansCaenorhabditis elegans ProteinsCaloric RestrictionFood DeprivationGenesHelminthLongevityPlasmidsRNA InterferenceVesicular Transport Proteins

Affiliated Institutions

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Publication Info

Year
2007
Type
article
Volume
3
Issue
6
Pages
597-599
Citations
334
Access
Closed

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334
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3
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288
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Cite This

Kailiang Jia, Beth Levine (2007). Autophagy is Required for Dietary Restriction-Mediated Life Span Extension in<i>C. elegans</i>. Autophagy , 3 (6) , 597-599. https://doi.org/10.4161/auto.4989

Identifiers

DOI
10.4161/auto.4989
PMID
17912023

Data Quality

Data completeness: 86%