Evidence map›Paper›PMID 25220459›Full record

ArticleCell reports2014

A mitochondrial ATP synthase subunit interacts with TOR signaling to modulate protein homeostasis and lifespan in Drosophila.

Xiaoping Sun, Charles T Wheeler, Jason Yolitz, Mara Laslo, Thomas Alberico, Yaning Sun, Qisheng Song, Sige Zou

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dynamic Changes in Gene Expression Through Aging inbioRxiv : the preprint server for biology · 2024
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

8 authors at 2 institutions in 1 country.

Xiaoping SunTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Charles T WheelerTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Jason YolitzTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Mara LasloTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Thomas AlbericoTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Yaning SunTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA.
Qisheng SongDivision of Plant Sciences, University of Missouri, Columbia, MO 65211, USA.
Sige ZouTranslational Gerontology Branch, National Institute on Aging, Baltimore, MD 21224, USA. Electronic address: zous@mail.nih.gov.
National Institute on Aging · USUniversity of Missouri · US

Funding

Functional Genomic Study of Aging and Aging InterventionsZIAAG000365 · NIA · NATIONAL INSTITUTE ON AGING · PI ZOU, SIGE · 2009 to 2015
$3.7M
Functional Genomic Study of Aging and Aging InterventionsZ01AG000365 · NIA · NATIONAL INSTITUTE ON AGING · PI ZOU, SIGE · 2005 to 2008
$1.1M
Intramural NIH HHS Z01 AG000365Intramural NIH HHS ZIA AG000365NIA NIH HHS AG000365-09
6 · The paper itself

Abstract

Diet composition is a critical determinant of lifespan, and nutrient imbalance is detrimental to health. However, how nutrients interact with genetic factors to modulate lifespan remains elusive. We investigated how diet composition influences mitochondrial ATP synthase subunit d (ATPsyn-d) in modulating lifespan in Drosophila. ATPsyn-d knockdown extended lifespan in females fed low carbohydrate-to-protein (C:P) diets but not the high C:P ratio diet. This extension was associated with increased resistance to oxidative stress; transcriptional changes in metabolism, proteostasis, and immune genes; reduced protein damage and aggregation, and reduced phosphorylation of S6K and ERK in TOR and mitogen-activated protein kinase (MAPK) signaling, respectively. ATPsyn-d knockdown did not extend lifespan in females with reduced TOR signaling induced genetically by Tsc2 overexpression or pharmacologically by rapamycin. Our data reveal a link among diet, mitochondria, and MAPK and TOR signaling in aging and stresses the importance of considering genetic background and diet composition in implementing interventions for promoting healthy aging.

Indexed as

AnimalsCell Cycle ProteinsDiet, Carbohydrate-RestrictedDrosophilaDrosophila ProteinsFemaleGene Expression RegulationHormone AntagonistsLongevityMetabolic Networks and PathwaysMifepristoneMitochondriaMitochondrial Proton-Translocating ATPasesOxidative StressPhosphorylationRNA InterferenceCell Cycle ProteinsDrosophila Proteinsgig protein, DrosophilaHormone AntagonistsMifepristoneMitochondrial Proton-Translocating ATPasesSirolimusTOR Serine-Threonine Kinases

Identifiers

PMID25220459
PMCPMC4177368
OpenAlexW2079155221

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.