Evidence map›Paper›PMID 28249716›Full record

ArticleMechanisms of ageing and development2017

Conserved effect of aging on DNA methylation and association with EZH2 polycomb protein in mice and humans.

Khyobeni Mozhui, Ashutosh K Pandey

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of ageing and development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Sex-specific modulation of renal epigenetic and injury markers in aging kidney.American journal of physiology. Renal physiology · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. DNA methylation clocks for dogs and humans.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Review
  17. Epigenetics of Aging and Aging-Associated Diseases.International journal of molecular sciences · 2021
    Review
  18. Frontiers in veterinary science · 2021
    Article
  19. 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

2 authors at 1 institution in 1 country.

Khyobeni MozhuiDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USA; Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA. Electronic address: kmozhui@uthsc.edu.
Ashutosh K PandeyCenter for Integrative and Translational Genomics, University of Tennessee Health Science Center, Memphis, TN, USA.
University of Tennessee Health Science Center · US

Funding

Translational Systems Genetics of Mitochondria, Metabolism, and AgingR01AG043930 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WILLIAMS, ROBERT W. · 2013 to 2017
$2.5M
NIA NIH HHS R01 AG043930
6 · The paper itself

Abstract

In humans, DNA methylation at specific CpG sites can be used to estimate the 'epigenetic clock', a biomarker of aging and health. The mechanisms that regulate the aging epigenome and level of conservation are not entirely clear. We performed affinity-based enrichment with methyl-CpG binding domain protein followed by high-throughput sequencing (MBD-seq) to assay DNA methylation in mouse samples. Consistent with previous reports, aging is associated with increase in methylation at CpG islands that likely overlap regulatory regions of genes that have been implicated in cancers (e.g., C1ql3, Srd5a2 and Ptk7). The differentially methylated regions in mice have high sequence conservation in humans and the pattern of methylation is also largely conserved between the two species. Based on human ENCODE data, these sites are targeted by polycomb proteins, including EZH2. Chromatin immunoprecipitation confirmed that these regions interact with EZH2 in mice as well, and there may be reduction in EZH2 occupancy with age at C1ql3. This adds to the growing evidence that EZH2 is part of the protein machinery that shapes the aging epigenome. The conservation in both sequence and methylation patterns of the age-dependent CpGs indicate that the epigenetic clock is a fundamental feature of aging in mammals.

Indexed as

3-Oxo-5-alpha-Steroid 4-DehydrogenaseAgingAnimalsCell Adhesion MoleculesCpG IslandsDNA MethylationEnhancer of Zeste Homolog 2 ProteinHumansMembrane ProteinsMiceReceptor Protein-Tyrosine Kinases3-Oxo-5-alpha-Steroid 4-DehydrogenaseCell Adhesion MoleculesEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanEzh2 protein, mouseMembrane ProteinsPTK7 protein, humanPtk7 protein, mouseReceptor Protein-Tyrosine KinasesSRD5A2 protein, humanSrd5a2 protein, mouseDNA methylationEpigeneticsEZH2MBD sequencingPolycomb repressive complex

Identifiers

PMID28249716
PMCPMC5411177
OpenAlexW2592701460

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.