Evidence map›Paper›PMID 30274593›Full record

ArticleeLife2018

Tri-methylation of histone H3 lysine 4 facilitates gene expression in ageing cells.

Cristina Cruz, Monica Della Rosa, Christel Krueger, Qian Gao, Dorottya Horkai, Michelle King, Lucy Field, Jonathan Houseley

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. International journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Epigenetic regulation of pulmonary inflammation.Seminars in cell & developmental biology · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Genomic Instability and Epigenetic Changes during Aging.International journal of molecular sciences · 2023
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  20. Article
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

8 authors at 1 institution in 1 country.

Cristina Cruz *Epigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.ORCID 0000-0001-7339-5355
Monica Della Rosa *Epigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.
Christel KruegerEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.ORCID 0000-0001-5601-598X
Qian GaoEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.
Dorottya HorkaiEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.
Michelle KingEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.
Lucy FieldEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.
Jonathan HouseleyEpigenetics Programme, The Babraham Institute, Cambridge, United Kingdom.ORCID 0000-0001-8509-1500
Babraham Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/0000H247Biotechnology and Biological Sciences Research Council BBS/E/B/000C0423Biotechnology and Biological Sciences Research Council BI Core Capability GrantH2020 European Research Council EpiGeneSys NetworkWellcome 088335,110216Wellcome TrustWellcome Trust 088335Wellcome Trust 110216
6 · The paper itself

Abstract

Transcription of protein coding genes is accompanied by recruitment of COMPASS to promoter-proximal chromatin, which methylates histone H3 lysine 4 (H3K4) to form H3K4me1, H3K4me2 and H3K4me3. Here, we determine the importance of COMPASS in maintaining gene expression across lifespan in budding yeast. We find that COMPASS mutations reduce replicative lifespan and cause expression defects in almost 500 genes. Although H3K4 methylation is reported to act primarily in gene repression, particularly in yeast, repressive functions are progressively lost with age while hundreds of genes become dependent on H3K4me3 for full expression. Basal and inducible expression of these genes is also impaired in young cells lacking COMPASS components Swd1 or Spp1. Gene induction during ageing is associated with increasing promoter H3K4me3, but H3K4me3 also accumulates in non-promoter regions and the ribosomal DNA. Our results provide clear evidence that H3K4me3 is required to maintain normal expression of many genes across organismal lifespan.

Indexed as

Transcription, GeneticAgingChromatinGene Expression Regulation, FungalHistone-Lysine N-MethyltransferaseHistonesProtein Processing, Post-TranslationalSaccharomyces cerevisiaeChromatinHistone-Lysine N-MethyltransferaseHistonesageingchromosomesCOMPASSgene expressionhistonemethylationS. cerevisiae

Identifiers

PMID30274593
PMCPMC6168286
OpenAlexW2784117710

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.