Evidence map›Paper›PMID 21834846›Full record

ArticleAging cell2011

The H3K27 demethylase UTX-1 regulates C. elegans lifespan in a germline-independent, insulin-dependent manner.

Travis J Maures, Eric L Greer, Anna G Hauswirth, Anne Brunet

Abstract read
In one paragraph

Article in Aging cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 148 papers.

0numbers the graph read from it
0cells of the map it votes in
148citing papers in PubMed
4.2field-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

148 citing papers in PubMed, 259 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Autophagy: The convergence point of aging and cancer.Biochemistry and biophysics reports · 2025
    Review
  5. Review
  6. Review
  7. An Update on Neuroaging on Earth and in Spaceflight.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Biomolecules · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Genomic Instability and Epigenetic Changes during Aging.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review

88 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

4 authors at 1 institution in 1 country.

Travis J MauresDepartment of Genetics, Stanford University, 300 Pasteur Drive, Stanford, CA 94305, USA.
Eric L Greer
Anna G Hauswirth
Anne Brunet
Stanford University · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Molecular mechanisms underlying lifespan extension by dietary restrictionR01AG031198 · NIA · STANFORD UNIVERSITY · PI BRUNET, ANNE · 2009 to 2013
$2.0M
Molecular Mechanisms Underlying Lifespan Extension by Environmental StimuliR56AG031198 · NIA · STANFORD UNIVERSITY · PI BRUNET, ANNE · 2015 to 2015
$438k
To determine the mechanism by which regulators of histone methylation control orgF32AG037254 · NIA · STANFORD UNIVERSITY · PI MAURES, TRAVIS JUSTIN · 2010 to 2012
$110k
NCI NIH HHS T32 CA009302NCI NIH HHS T32-CA009302NHGRI NIH HHS T32 HG000044NHGRI NIH HHS T32-HG000044NIA NIH HHS AG31198NIA NIH HHS F32 AG037254NIA NIH HHS F32-AG037254NIA NIH HHS R01 AG031198NIA NIH HHS R01-AG31198NIA NIH HHS R56 AG031198
6 · The paper itself

Abstract

Aging is accompanied by alterations in epigenetic marks that control chromatin states, including histone acetylation and methylation. Enzymes that reversibly affect histone marks associated with active chromatin have recently been found to regulate aging in Caenorhabditis elegans. However, relatively little is known about the importance for aging of histone marks associated with repressed chromatin. Here, we use a targeted RNAi screen in C. elegans to identify four histone demethylases that significantly regulate worm lifespan, UTX-1, RBR-2, LSD-1, and T26A5.5. Interestingly, UTX-1 belongs to a conserved family of histone demethylases specific for lysine 27 of histone H3 (H3K27me3), a mark associated with repressed chromatin. Both utx-1 knockdown and heterozygous mutation of utx-1 extend lifespan and increase the global levels of the H3K27me3 mark in worms. The H3K27me3 mark significantly drops in somatic cells during the normal aging process. UTX-1 regulates lifespan independently of the presence of the germline, but in a manner that depends on the insulin-FoxO signaling pathway. These findings identify the H3K27me3 histone demethylase UTX-1 as a novel regulator of worm lifespan in somatic cells.

Indexed as

Gene Expression RegulationLongevityAnimalsBiomarkersBlotting, WesternCaenorhabditis elegansChromatinGene Knockdown TechniquesGerm CellsHigh-Throughput Screening AssaysHistone DemethylasesHistonesInsulinMethylationPolymerase Chain ReactionRNA InterferenceBiomarkersChromatinHistone DemethylasesHistonesInsulinTranscription Factors

Identifiers

PMID21834846
PMCPMC3215905
OpenAlexW1508556872

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.