Evidence map›Paper›PMID 26647291›Full record

ArticleAging2015

RPD3 histone deacetylase and nutrition have distinct but interacting effects on Drosophila longevity.

Stewart Frankel, Jared Woods, Tahereh Ziafazeli, Blanka Rogina

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Evolution, Chance, and Aging.Frontiers in genetics · 2021
    Review
  5. The Epigenetics of Aging in Invertebrates.International journal of molecular sciences · 2019
    Review
  6. Article
  7. Article
  8. The effects of reducedNutrition and healthy aging · 2017
    Article
  9. Review
  10. Aging · 2016
    Article
  11. Epigenetics and aging.Science advances · 2016
    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

4 authors at 2 institutions in 2 countries.

Stewart FrankelDepartment of Biology, University of Hartford, West Hartford, CT 06117, USA.
Jared WoodsDepartment of Genetics and Genome Sciences, School of Medicine, University of Connecticut Health, Farmington, CT 06030, USA.
Tahereh ZiafazeliDepartment of Genetics and Genome Sciences, School of Medicine, University of Connecticut Health, Farmington, CT 06030, USA.
Blanka RoginaDepartment of Genetics and Genome Sciences, School of Medicine, University of Connecticut Health, Farmington, CT 06030, USA.
UConn Health · USUniversity of Hartford · US

Funding

Molecular Genetics of Caloric Restriction in Aging FliesR01AG023088 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ROGINA, BLANKA · 2004 to 2013
$3.2M
NIA NIH HHS AG023088NIA NIH HHS R01 AG023088
6 · The paper itself

Abstract

Single-gene mutations that extend longevity have revealed regulatory pathways related to aging and longevity. RPD3 is a conserved histone deacetylase (Class I HDAC). Previously we showed that Drosophila rpd3 mutations increase longevity. Here we tested the longevity effects of RPD3 on multiple nutrient levels. Dietary restriction (DR) has additive effects on RPD3-mediated longevity extension, but the effect may be modestly attenuated relative to controls. RPD3 and DR therefore appear to operate by distinct but interacting mechanisms. Since RPD3 regulates transcription, the mRNA levels for two proteins involved in nutrient signaling, 4E-BP and Tor, were examined in rpd3 mutant flies. 4E-BP mRNA was reduced under longevity-increasing conditions. Epistasis between RPD3 and 4E-BP with regard to longevity was then tested. Flies only heterozygous for a mutation in Thor, the 4E-BP gene, have modestly decreased life spans. Flies mutant for both rpd3 and Thor show a superposition of a large RPD3-mediated increase and a small Thor-mediated decrease in longevity at all food levels, consistent with each gene product having distinct effects on life span. However, DR-mediated extension was absent in males carrying both mutations and lessened in females. Our results support the view that multiple discrete but interacting mechanisms regulate longevity.

Indexed as

Animal FeedAnimalsDrosophila melanogasterDrosophila ProteinsFemaleGene Expression RegulationGenotypeHistone Deacetylase 1LongevityMaleMutationSignal TransductionDrosophila ProteinsHDAC1 protein, DrosophilaHistone Deacetylase 1agingdietary restrictionDrosophilalongevityRpd3

Identifiers

PMID26647291
PMCPMC4712336
OpenAlexW2191347852

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.