Document Detail


Autophagy and leucine promote chronological longevity and respiration proficiency during calorie restriction in yeast.
MedLine Citation:
PMID:  23337777     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We have previously shown that autophagy is required for chronological longevity in the budding yeast Saccharomyces cerevisiae. Here we examine the requirements for autophagy during extension of chronological life span (CLS) by calorie restriction (CR). We find that autophagy is upregulated by two CR interventions that extend CLS: water wash CR and low glucose CR. Autophagy is required for full extension of CLS during water wash CR under all growth conditions tested. In contrast, autophagy was not uniformly required for full extension of CLS during low glucose CR, depending on the atg allele and strain genetic background. Leucine status influenced CLS during CR. Eliminating the leucine requirement in yeast strains or adding supplemental leucine to growth media extended CLS during CR. In addition, we observed that both water wash and low glucose CR promote mitochondrial respiration proficiency during aging of autophagy-deficient yeast. In general, the extension of CLS by water wash or low glucose CR was inversely related to respiration deficiency in autophagy-deficient cells. Also, autophagy is required for full extension of CLS under non-CR conditions in buffered media, suggesting that extension of CLS during CR is not solely due to reduced medium acidity. Thus, our findings show that autophagy is: (1) induced by CR, (2) required for full extension of CLS by CR in most cases (depending on atg allele, strain, and leucine availability) and, (3) promotes mitochondrial respiration proficiency during aging under CR conditions.
Authors:
John P Aris; Ashley L Alvers; Roy A Ferraiuolo; Laura K Fishwick; Amanda Hanvivatpong; Doreen Hu; Christine Kirlew; Michael T Leonard; Kyle J Losin; Michelle Marraffini; Arnold Y Seo; Veronica Swanberg; Jennifer L Westcott; Michael S Wood; Christiaan Leeuwenburgh; William A Dunn
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2013-01-18
Journal Detail:
Title:  Experimental gerontology     Volume:  48     ISSN:  1873-6815     ISO Abbreviation:  Exp. Gerontol.     Publication Date:  2013 Oct 
Date Detail:
Created Date:  2013-09-02     Completed Date:  2014-03-11     Revised Date:  2014-10-12    
Medline Journal Info:
Nlm Unique ID:  0047061     Medline TA:  Exp Gerontol     Country:  England    
Other Details:
Languages:  eng     Pagination:  1107-19     Citation Subset:  IM    
Copyright Information:
Copyright © 2013 Elsevier Inc. All rights reserved.
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MeSH Terms
Descriptor/Qualifier:
Autophagy / physiology*
Blotting, Western
Caloric Restriction*
Cell Division / physiology
Culture Media
DNA Damage / physiology
Galactose / metabolism
Glucose / metabolism
Hydrogen-Ion Concentration
Leucine / physiology*
Oxidative Stress / physiology
Oxygen Consumption / physiology*
Saccharomyces cerevisiae / growth & development,  physiology*
Time Factors
Up-Regulation
Grant Support
ID/Acronym/Agency:
AG023719/AG/NIA NIH HHS; AG17994/AG/NIA NIH HHS; AG21042/AG/NIA NIH HHS; R01 AG017994/AG/NIA NIH HHS; R01 AG021042/AG/NIA NIH HHS; R21 AG023719/AG/NIA NIH HHS
Chemical
Reg. No./Substance:
0/Culture Media; GMW67QNF9C/Leucine; IY9XDZ35W2/Glucose; X2RN3Q8DNE/Galactose
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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