Evidence map›Paper›PMID 18221413›Full record

ArticleAging cell2008

Drosophila lifespan control by dietary restriction independent of insulin-like signaling.

Kyung-Jin Min, Rochele Yamamoto, Susanne Buch, Michael Pankratz, Marc Tatar

Open access · bronzeAbstract read
In one paragraph

Article in Aging cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

107 citing papers in PubMed, 189 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. The landscape of aging.Science China. Life sciences · 2022
    Review
  7. Amino Acid Availability Is Not Essential for Life-Span Extension by Dietary Restriction in the Fly.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Aging mechanisms-A perspective mostly fromAdvanced genetics (Hoboken, N.J.) · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

47 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

5 authors at 2 institutions in 3 countries.

Kyung-Jin MinDepartment of Ecology and Evolutionary Biology, Division of Biology and Medicine, Brown University, Providence, RI 02912, USA.
Rochele Yamamoto
Susanne Buch
Michael Pankratz
Marc Tatar
Brown University · USFZI Research Center for Information Technology · DE

Funding

FUNCTIONS AND INTERACTIONS DFOXO IN DROSOPHILA AGINGR37AG024360 · NIA · BROWN UNIVERSITY · PI TATAR, MARC · 2011 to 2020
$4.5M
Regulatory systems of Drosophila agingR01AG021953 · NIA · BROWN UNIVERSITY · PI TATAR, MARC · 2003 to 2007
$1.9M
Functions and Interactions dFOXO in Drosopila AgingR01AG024360 · NIA · BROWN UNIVERSITY · PI TATAR, MARC · 2004 to 2010
$1.7M
NIA NIH HHS AG021953NIA NIH HHS AG024360NIA NIH HHS R01 AG021953NIA NIH HHS R01 AG024360NIA NIH HHS R37 AG024360
6 · The paper itself

Abstract

Reduced insulin/insulin-like growth factor (IGF) signaling may be a natural way for the reduction of dietary nutrients to extend lifespan. While evidence challenging this hypothesis is accumulating with Caenorhabditis elegans, for Drosophila melanogaster it is still thought that insulin/IGF and the mechanisms of dietary restriction (DR) might as yet function through overlapping mechanisms. Here, we aim to understand this potential overlap. We found that over-expression of dFOXO in head fat body extends lifespan and reduces steady-state mRNA abundance of insulin-like peptide-2 under conditions of high dietary yeast, but not when yeast is limiting. In contrast, conditions of DR that increase lifespan change only insulin-like peptide-5 (ilp5) mRNA abundance. Thus, reduction of ilp5 mRNA is associated with longevity extension by DR, while reduction of insulin-like peptide-2 is associated with the diet-dependent effects of FOXO over-expression upon lifespan. To assess whether reduction of ilp5 is required for DR to extend lifespan, we blocked its diet-dependent change with RNAi. Loss of the ilp5 dietary response did not diminish the capacity of DR to extend lifespan. Finally, we assessed the capacity of DR to extend lifespan in the absence of dFOXO, the insulin/IGF-responsive transcription factor. As with the knockdown of ilp5 diet responsiveness, DR was equally effective among genotypes with and without dFOXO. It is clear from many Drosophila studies that insulin/IGF mediates growth and metabolic responses to nutrition, but we now find no evidence that this endocrine system mediates the interaction between dietary yeast and longevity extension.

Indexed as

Animal Nutritional Physiological PhenomenaAnimalsCaloric RestrictionDiet, ReducingDrosophila melanogasterDrosophila ProteinsFat BodyFemaleForkhead Transcription FactorsGene ExpressionGenetic EngineeringHeadInsulinLongevityModels, AnimalProteinsDrosophila ProteinsForkhead Transcription FactorsFOXO protein, DrosophilaInsulinLeydig insulin-like proteinProteins

Identifiers

PMID18221413
PMCPMC2340190
OpenAlexW2071206597

What OpenQuestion holds

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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.