Evidence map›Paper›PMID 24859460›Full record

ReviewBiochimica et biophysica acta2014

Histone methylation and aging: lessons learned from model systems.

Brenna S McCauley, Weiwei Dang

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 93 citations in OpenAlex.

  1. Histone modification clocks for robust cross-species biological age prediction and elucidating senescence regulation.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  15. Caloric restriction induced epigenetic effects on aging.Frontiers in cell and developmental biology · 2022
    Review
  16. Article
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  18. Balancing DNA repair to prevent ageing and cancer.Experimental cell research · 2021
    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

2 authors at 1 institution in 1 country.

Brenna S McCauleyHuffington Center on Aging, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA. Electronic address: brenna.mccauley@bcm.edu.
Weiwei DangHuffington Center on Aging, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA. Electronic address: weiwei.dang@bcm.edu.
Baylor College of Medicine · US

Funding

Regulation of yeast cellular aging through chromatin and novel pathwaysR00AG037646 · NIA · BAYLOR COLLEGE OF MEDICINE · PI DANG, WEIWEI · 2013 to 2015
$740k
NIA NIH HHS R00 AG037646NIA NIH HHS R00AG037646
6 · The paper itself

Abstract

Aging induces myriad cellular and, ultimately, physiological changes that cause a decline in an organism's functional capabilities. Although the aging process and the pathways that regulate it have been extensively studied, only in the last decade have we begun to appreciate that dynamic histone methylation may contribute to this process. In this review, we discuss recent work implicating histone methylation in aging. Loss of certain histone methyltransferases and demethylases changes lifespan in invertebrates, and alterations in histone methylation in aged organisms regulate lifespan and aging phenotypes, including oxidative stress-induced hormesis in yeast, insulin signaling in Caenorhabiditis elegans and mammals, and the senescence-associated secretory phenotype in mammals. In all cases where histone methylation has been shown to impact aging and aging phenotypes, it does so by regulating transcription, suggesting that this is a major mechanism of its action in this context. Histone methylation additionally regulates or is regulated by other cellular pathways that contribute to or combat aging. Given the numerous processes that regulate aging and histone methylation, and are in turn regulated by them, the role of histone methylation in aging is almost certainly underappreciated.

Indexed as

AgingAnimalsDNA MethylationHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesHumansMethylationModels, BiologicalProgeriaProtein Processing, Post-TranslationalHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesAgingEpigeneticsHistone methylation

Identifiers

PMID24859460
PMCPMC4240748
OpenAlexW2023752776

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.