Evidence map›Paper›PMID 20146810›Full record

ArticleBMC biology2010

A metabolic signature of long life in Caenorhabditis elegans.

Silke Fuchs, Jacob G Bundy, Sarah K Davies, Jonathan M Viney, Jonathan S Swire, Armand M Leroi

Abstract read
In one paragraph

Article in BMC biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
–field-weighted citation impact
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

96 citing papers in PubMed.

  1. Article
  2. Metabolomic Profiling ofJournal of fungi (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Phenotypic and metabonomics studies of FMOs in C. elegans and their roles in lifespan extension.Metabolomics : Official journal of the Metabolomic Society · 2025
    Article
  5. Article
  6. Genetic mapping of lifespan and mitochondrial stress response inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Self-DNA inMolecules (Basel, Switzerland) · 2024
    Article
  10. Multi-Omics Integrative Analysis to Reveal the Impacts ofInternational journal of molecular sciences · 2024
    Article
  11. The Native Microbiome MemberMetabolites · 2023
    Article
  12. Article
  13. The metabolic contribution of SKN-1/Nrf2 to the lifespan of Caenorhabditis elegans.Metabolomics : Official journal of the Metabolomic Society · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. AFrontiers in microbiology · 2022
    Article

36 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

6 authors.

Silke FuchsDivision of Biology, Silwood Park Campus, Imperial College London, UK.
Jacob G Bundy
Sarah K Davies
Jonathan M Viney
Jonathan S Swire
Armand M Leroi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany Caenorhabditis elegans mutations increase longevity and much evidence suggests that they do so at least partly via changes in metabolism. However, up until now there has been no systematic investigation of how the metabolic networks of long-lived mutants differ from those of normal worms. Metabolomic technologies, that permit the analysis of many untargeted metabolites in parallel, now make this possible. Here we use one of these, 1H nuclear magnetic resonance spectroscopy, to investigate what makes long-lived worms metabolically distinctive.

resultsWe examined three classes of long-lived worms: dauer larvae, adult Insulin/IGF-1 signalling (IIS)-defective mutants, and a translation-defective mutant. Surprisingly, these ostensibly different long-lived worms share a common metabolic signature, dominated by shifts in carbohydrate and amino acid metabolism. In addition the dauer larvae, uniquely, had elevated levels of modified amino acids (hydroxyproline and phosphoserine). We interrogated existing gene expression data in order to integrate functional (metabolite-level) changes with transcriptional changes at a pathway level.

conclusionsThe observed metabolic responses could be explained to a large degree by upregulation of gluconeogenesis and the glyoxylate shunt as well as changes in amino acid catabolism. These responses point to new possible mechanisms of longevity assurance in worms. The metabolic changes observed in dauer larvae can be explained by the existence of high levels of autophagy leading to recycling of cellular components.See associated minireview: http://jbiol.com/content/9/1/7.

Indexed as

Amino AcidsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCarbohydrate MetabolismGluconeogenesisGlyoxylatesInsulinInsulin-Like Growth Factor ILarvaLongevityMagnetic Resonance SpectroscopyModels, BiologicalMutationReceptor, InsulinAmino AcidsCaenorhabditis elegans ProteinsDAF-2 protein, C elegansGlyoxylatesglyoxylic acidInsulinInsulin-Like Growth Factor IReceptor, Insulin

Identifiers

PMID20146810
PMCPMC2829508

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Registered trials

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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.