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Histone methylation makes its mark on longevity
Open accessAbstract
How long organisms live is not entirely written in their genes. Recent findings reveal that epigenetic factors that regulate histone methylation, a type of chromatin modification, can affect lifespan. The reversible nature of chromatin modifications suggests that therapeutic targeting of chromatin regulators could be used to extend lifespan and healthspan. This review describes the epigenetic regulation of lifespan in diverse model organisms, focusing on the role and mode of action of chromatin regulators that affect two epigenetic marks, trimethylated lysine 4 of histone H3 (H3K4me3) and trimethylated lysine 27 of histone H3 (H3K27me3), in longevity.
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“Increased histone H4K16 acetylation, H4K20 trimethylation or H3K4 trimethylation, as well as decreased H3K9 methylation or H3K27 trimethylation, constitute age-associated epigenetic marks (Fraga and Esteller, 2007; Han and Brunet, 2012).”
From The Hallmarks of Aging (2013) · cites this paper as Han and Brunet, 2012
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“For example, the ASH-2 trithorax complex mediates trimethylation of histone H3 on Lys4 (H3K4me3), and its deletion increases Caenorhabditis elegans lifespan, consistent with excessive H3K4me3 being associated with an aging epigenome172,173.”
From Stem cell aging: mechanisms, regulators and therapeutic opportunities (2014) · cites this paper as [173]
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Metadata
- Authors
- Han, S., & Brunet, A.
- Affiliations
- Stanford University (US)
- Corresponding author
- Brunet, Anne
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2012-01
- Volume
- 22
- Issue
- 1
- Pages
- 42-49
- ISSN
- 0962-8924 (ISSN-L)
- PMC
- PMC3253950
- OpenAlex
- W1968018974
- Cited by
- 204
- References
- 93
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 5 · 2023: 17 · 2022: 14 · 2021: 13 · 2020: 13 · 2019: 11 · 2018: 20 · 2017: 19 · 2016: 15 · 2015: 18 · 2014: 17 · 2013: 17 · 2012: 6
- FWCI
- 1.34
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Trends in Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation
- National Institutes of Health
- National Institute on Aging (R01-AG31198, R01AG031198)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- histone methylation, lifespan, longevity, epigenetic regulation, chromatin modification, H3K4me3, H3K27me3, chromatin regulators, healthspan, model organisms
- MeSH terms
- Animals, Chromatin, Histones, Humans, Longevity, Methylation, Phylogeny, Cellular Senescence
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