Evidence map›Paper›PMID 19302372›Full record

ArticleAging cell2009

Autophagy and amino acid homeostasis are required for chronological longevity in Saccharomyces cerevisiae.

Ashley L Alvers, Laura K Fishwick, Michael S Wood, Doreen Hu, Hye S Chung, William A Dunn, John P Aris

Open access · bronzeAbstract read
In one paragraph

Article in Aging cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 226 citations in OpenAlex.

  1. Article
  2. The YeastInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Metabolic Biomarkers for Lifespan Extension and Cellular Stress inPreventive nutrition and food science · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cardiovascular aging: the mitochondrial influence.The journal of cardiovascular aging · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Quiescence inAnnual review of genetics · 2022
    Review
  17. Article
  18. Article
  19. Review
  20. Article

77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Ashley L AlversDepartment of Anatomy and Cell Biology, Health Science Center, University of Florida, Gainesville, 32610-0235, USA.
Laura K Fishwick
Michael S Wood
Doreen Hu
Hye S Chung
William A Dunn
John P Aris
University of Florida Health Science Center · USDuke University · US

Funding

Regulation of Yeast Life SpanR21AG023719 · NIA · UNIVERSITY OF FLORIDA · PI ARIS, JOHN P · 2005 to 2006
$319k
NIA NIH HHS AG023719NIA NIH HHS R21 AG023719
6 · The paper itself

Abstract

Following cessation of growth, yeast cells remain viable in a nondividing state for a period of time known as the chronological lifespan (CLS). Autophagy is a degradative process responsible for amino acid recycling in response to nitrogen starvation and amino acid limitation. We have investigated the role of autophagy during chronological aging of yeast grown in glucose minimal media containing different supplemental essential and nonessential amino acids. Deletion of ATG1 or ATG7, both of which are required for autophagy, reduced CLS, whereas deletion of ATG11, which is required for selective targeting of cellular components to the vacuole for degradation, did not reduce CLS. The nonessential amino acids isoleucine and valine, and the essential amino acid leucine, extended CLS in autophagy-deficient as well as autophagy-competent yeast. This extension was suppressed by constitutive expression of GCN4, which encodes a transcriptional regulator of general amino acid control (GAAC). Consistent with this, GCN4 expression was reduced by isoleucine and valine. Furthermore, elimination of the leucine requirement extended CLS and prevented the effects of constitutive expression of GCN4. Interestingly, deletion of LEU3, a GAAC target gene encoding a transcriptional regulator of branched side chain amino acid synthesis, dramatically increased CLS in the absence of amino acid supplements. In general, this indicates that activation of GAAC reduces CLS whereas suppression of GAAC extends CLS in minimal medium. These findings demonstrate important roles for autophagy and amino acid homeostasis in determining CLS in yeast.

Indexed as

AutophagyHomeostasis3-Isopropylmalate DehydrogenaseAgingAmino AcidsBasic-Leucine Zipper Transcription FactorsCulture MediaDown-RegulationGene Expression Regulation, FungalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTrans-Activators3-Isopropylmalate DehydrogenaseAmino AcidsBasic-Leucine Zipper Transcription FactorsCulture MediaGCN4 protein, S cerevisiaeLEU2 protein, S cerevisiaeLEU3 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTrans-Activators

Identifiers

PMID19302372
PMCPMC2802268
OpenAlexW2160751669

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.