Evidence map›Paper›PMID 29912876›Full record

ArticlePLoS genetics2018

Unique patterns of trimethylation of histone H3 lysine 4 are prone to changes during aging in Caenorhabditis elegans somatic cells.

Mintie Pu, Minghui Wang, Wenke Wang, Satheeja Santhi Velayudhan, Siu Sylvia Lee

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. 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
1.8field-weighted citation impact, top 15% 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, 51 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Genetic and Epigenetic Interactions Involved in Senescence of Stem Cells.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Genomic Instability and Epigenetic Changes during Aging.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  15. Article
  16. Article
  17. Chromatin: the old and young of it.Frontiers in molecular biosciences · 2023
    Review
  18. Review
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Mintie PuDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York City, United States of America.ORCID 0000-0001-9654-8633
Minghui WangComputational Biology Service Unit, Cornell University, Ithaca, New York City, United States of America.
Wenke WangDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York City, United States of America.
Satheeja Santhi VelayudhanDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York City, United States of America.ORCID 0000-0002-9448-2105
Siu Sylvia LeeDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York City, United States of America.
Cornell University · US

Funding

Systematic Analysis of C elegans Longevity DeterminantsR01AG024425 · NIA · CORNELL UNIVERSITY ITHACA · PI Siu Sylvia Lee · 2004 to 2026
$8.5M
NIA NIH HHS R01 AG024425
6 · The paper itself

Abstract

Tri-methylation on histone H3 lysine 4 (H3K4me3) is associated with active gene expression but its regulatory role in transcriptional activation is unclear. Here we used Caenorhabditis elegans to investigate the connection between H3K4me3 and gene expression regulation during aging. We uncovered around 30% of H3K4me3 enriched regions to show significant and reproducible changes with age. We further showed that these age-dynamic H3K4me3 regions largely mark gene-bodies and are acquired during adult stages. We found that these adult-specific age-dynamic H3K4me3 regions are correlated with gene expression changes with age. In contrast, H3K4me3 marking established during developmental stages remained largely stable with age, even when the H3K4me3 associated genes exhibited RNA expression changes during aging. Importantly, the genes associated with changes in H3K4me3 and RNA levels with age are enriched for functional groups commonly implicated in aging biology. Therefore, our findings suggested divergent roles of H3K4me3 in gene expression regulation during aging, with important implications on aging-dependent pathophysiologies.

Indexed as

Age FactorsAnimalsCaenorhabditis elegansDNA MethylationEpigenesis, GeneticGene Expression RegulationHistonesLysineMethylationTranscriptional ActivationHistonesLysine

Identifiers

PMID29912876
PMCPMC6023244
OpenAlexW2809007605

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.