Evidence map›Paper›PMID 19239415›Full record

ArticleAging cell2009

NQR1 controls lifespan by regulating the promotion of respiratory metabolism in yeast.

María Jiménez-Hidalgo, Carlos Santos-Ocaña, Sergio Padilla, José M Villalba, Guillermo López-Lluch, Alejandro Martín-Montalvo, Robin K Minor, David A Sinclair, Rafael de Cabo, Plácido Navas

Open access · greenAbstract 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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. NQO1 Binds and Supports SIRT1 Function.Frontiers in pharmacology · 2021
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Calorie restriction as an intervention in ageing.The Journal of physiology · 2016
    Review
  13. CytochromeNPJ aging and mechanisms of disease · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Sirtuin activation: a role for plasma membrane in the cell growth puzzle.The journals of gerontology. Series A, Biological sciences and medical sciences · 2013
    Article
  19. Article
  20. Review
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

10 authors at 4 institutions in 2 countries.

María Jiménez-HidalgoCentro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide-CSIC and Centre for Biomedical Research on Rare Diseases (CIBERER), ISCIII, E-41013 Sevilla, Spain.
Carlos Santos-Ocaña
Sergio Padilla
José M Villalba
Guillermo López-Lluch
Alejandro Martín-Montalvo
Robin K Minor
David A Sinclair
Rafael de Cabo
Plácido Navas
Instituto de Salud Carlos III · ESNational Institute on Aging · USHarvard University · USUniversity of Córdoba · ES

Funding

Calorie restriction and agingZIAAG000368 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$6.9M
Role of Sgs1 DNA helicase in telomere maintenanceR01AG019719 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SINCLAIR, DAVID A. · 2001 to 2022
$5.3M
Aging and CR effects on the Plasma Membrane Redox SystemZIAAG000362 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2025
$5.0M
SIRT as a regulator of health and lifespan of mammalsR01AG028730 · NIA · HARVARD MEDICAL SCHOOL · PI SINCLAIR, DAVID A. · 2007 to 2011
$1.7M
Calorie restriction and agingZ01AG000368 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2005 to 2008
$1.4M
Intramural NIH HHS Z01 AG000368NIA NIH HHS R01 AG019719NIA NIH HHS R01 AG028730
6 · The paper itself

Abstract

The activity and expression of plasma membrane NADH coenzyme Q reductase is increased by calorie restriction (CR) in rodents. Although this effect is well-established and is necessary for CR's ability to delay aging, the mechanism is unknown. Here we show that the Saccharomyces cerevisiae homolog, NADH-Coenzyme Q reductase 1 (NQR1), resides at the plasma membrane and when overexpressed extends both replicative and chronological lifespan. We show that NQR1 extends replicative lifespan in a SIR2-dependent manner by shifting cells towards respiratory metabolism. Chronological lifespan extension, in contrast, occurs via an SIR2-independent decrease in ethanol production. We conclude that NQR1 is a key mediator of lifespan extension by CR through its effects on yeast metabolism and discuss how these findings could suggest a function for this protein in lifespan extension in mammals.

Indexed as

Cell MembraneCell RespirationCellular SenescenceElectron Transport Complex IEnergy MetabolismEthanolHistone DeacetylasesSaccharomyces cerevisiaeSilent Information Regulator Proteins, Saccharomyces cerevisiaeSirtuin 2SirtuinsElectron Transport Complex IEthanolHistone DeacetylasesSilent Information Regulator Proteins, Saccharomyces cerevisiaeSIR2 protein, S cerevisiaeSirtuin 2Sirtuins

Identifiers

PMID19239415
PMCPMC2699585
OpenAlexW1991149870

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.