Methylome analysis in long-lived men deciphers DNA methylation modifications associated with male longevity in humans

Men, despite having a lower likelihood of longevity compared to women, generally exhibit better health status when they achieve longevity. The role of DNA methylation in this paradox remains unclear. We performed whole-genome bisulfite sequencing on long-lived men (LLMs), long-lived women (LLWs), younger men (YMs) and younger women (YWs) to explore specific methylation characteristics in LLMs. Despite an accelerated methylation aging rate in LLMs compared to LLWs, we identify thousands of differentially methylated genomic units (DMUs) in LLMs independent of age and sex. These DMUs, validated by an elastic net classifier, can serve as methylation markers for discriminating longevity potential in men. Many are located near health-related genes. Genes like PIWIL1 and EXT1, with promoters featuring DMUs, exemplify the potential role of LLM-specific methylation patterns in suppressing age-related diseases by regulating gene transcription. Our findings provide evidence of a distinct methylation feature contributing to healthy aging and longevity of LLMs.

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Publication Details

Journal
Cell Reports
Published
2025-01-01
DOI
https://doi.org/10.1016/j.celrep.2024.115158
Citations
3
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
2.42
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article

Methylome analysis in long-lived men deciphers DNA methylation modifications associated with male longevity in humans

Qing‐Peng Kong, Fu‐Hui Xiao, Tianrui Xia, Liqin Yang et al.
3 citations
Cell Reports
Epigenetics and DNA Methylation
2.42
article

Methylome analysis in long-lived men deciphers DNA methylation modifications associated with male longevity in humans

Qing‐Peng Kong, Fu‐Hui Xiao, Tianrui Xia, Liqin Yang, Haotian Wang, Long Zhao, Siyu Ma
article en
3 citations

Abstract

Men, despite having a lower likelihood of longevity compared to women, generally exhibit better health status when they achieve longevity. The role of DNA methylation in this paradox remains unclear. We performed whole-genome bisulfite sequencing on long-lived men (LLMs), long-lived women (LLWs), younger men (YMs) and younger women (YWs) to explore specific methylation characteristics in LLMs. Despite an accelerated methylation aging rate in LLMs compared to LLWs, we identify thousands of differentially methylated genomic units (DMUs) in LLMs independent of age and sex. These DMUs, validated by an elastic net classifier, can serve as methylation markers for discriminating longevity potential in men. Many are located near health-related genes. Genes like PIWIL1 and EXT1, with promoters featuring DMUs, exemplify the potential role of LLM-specific methylation patterns in suppressing age-related diseases by regulating gene transcription. Our findings provide evidence of a distinct methylation feature contributing to healthy aging and longevity of LLMs.

Cell ReportsVol. 44(1)
Ningbo University (CN), Kunming Institute of Zoology (CN), Chinese Academy of Sciences (CN), University of Chinese Academy of Sciences (CN), University of Hong Kong (HK)
Zero hunger
Openalex Percentile: Top 14%
Epigenetics and DNA Methylation
2.42
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