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DNA methylation rates scale with maximum lifespan across mammals
Published version of a preprint
Abstract
DNA methylation rates have previously been found to broadly correlate with maximum lifespan in mammals, yet no precise relationship has been observed. We developed a statistically robust framework to compare methylation rates at conserved age-related sites across mammals. We found that methylation rates negatively scale with maximum lifespan in both blood and skin. The emergence of explicit scaling suggests that methylation rates are, or are linked to, an evolutionary constraint on maximum lifespan acting across diverse mammalian lineages.
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Long-lived animals share enhanced DNA repair, reduced molecular error rates and other processes.
“Long-lived animals share enhanced DNA repair3,5,9–11, reduced molecular error rates and other processes6,12–14.”
From A damage accumulation model identifies distinct aging regimes across species (2026) · cites this paper as [14]
Long-living mammals have enhanced repair and reduced error rates in several processes.
“Long-living mammals have indeed been found to have enhanced repair and reduced error rates in several processes (some of which may not drive aging).”
From A damage accumulation model identifies distinct aging regimes across species (2026) · cites this paper as [14]
Cellular error rates inverse to mammalian species lifespan include somatic mutations, epigenetic dysregulation, transcription and translation errors.
“Cellular error rates that have been found to be inverse to mammalian species lifespan include somatic mutations12, epigenetic dysregulation14, transcription and translation errors13.”
From A damage accumulation model identifies distinct aging regimes across species (2026) · cites this paper as [14]
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Kleiber, M. (1932) · Hilgardia · doi:10.3733/hilg.v06n11p315 · Cited by 2,222
Bocklandt, S., Lin, W., Sehl, M. E., Sánchez, F. J., Sinsheimer, J. S., Horvath, S., & Vilain, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014821 · Cited by 1,012
In Vivo Amelioration of Age-Associated Hallmarks by Partial Reprogramming.
Ocampo, A., Reddy, P., Martinez-Redondo, P., Platero-Luengo, A., Hatanaka, F., Hishida, T., Li, M., Lam, D., Kurita, M., Beyret, E., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.052 · Cited by 988
Somatic mutation rates scale with lifespan across mammals
Cagan, A., Baez-Ortega, A., Brzozowska, N., Abascal, F., Coorens, T. H. H., Sanders, M. A., Lawson, A. R. J., Harvey, L. M. R., Bhosle, S., Jones, D., et al. (2022) · Nature · doi:10.1038/s41586-022-04618-z · Cited by 481
DNA methylation networks underlying mammalian traits
Haghani, A., Li, C. Z., Robeck, T. R., Zhang, J., Lu, A. T., Ablaeva, J., Acosta-Rodríguez, V. A., Adams, D. M., Alagaili, A. N., Almunia, J., et al. (2023) · Science · doi:10.1126/science.abq5693 · Cited by 128
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Research works printed but not linked: 22
- West, G. B. & Brown, J. H. The origin of allometric scaling laws in biology from genomes to ecosystems: towards a quantitative unifying theory of biological structure and organization. J. Exp. Biol. 208, 1575–1592 (2005). · DOI
- West, G. B., Woodruff, W. H. & Brown, J. H. Allometric scaling of metabolic rate from molecules and mitochondria to cells and mammals. Proc. Natl Acad. Sci. USA 99, 2473–2478 (2002). · DOI
- West, G. B., Brown, J. H. & Enquist, B. J. A general model for the origin of allometric scaling laws in biology. Science 276, 122–126 (1997). · DOI · Paper page
- Hannum, G. et al. Genome-wide methylation profiles reveal quantitative views of human aging rates. Mol. Cell 49, 359–367 (2013). · DOI · Paper page
- Horvath, S. DNA methylation age of human tissues and cell types. Genome Biol. 14, R115 (2013). · DOI · Paper page
- Lu, A. T. et al. Universal DNA methylation age across mammalian tissues. Nat. Aging 3, 1144–1166 (2023). · DOI
- Lowe, R. et al. Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species. Genome Biol. 19, 22 (2018). · DOI
- Wilkinson, G. S. et al. DNA methylation predicts age and provides insight into exceptional longevity of bats. Nat. Commun. 12, 1615 (2021). · DOI
- Li, C. Z. et al. Epigenetic predictors of maximum lifespan and other life history traits in mammals. Preprint at bioRxiv https://doi.org/10.1101/2021.05.16.444078 (2021). · DOI
- Haghani, A. et al. Divergent age-related methylation patterns in long and short-lived mammals. Preprint at bioRxiv https://doi.org/10.1101/2022.01.16.476530 (2022). · DOI · Paper page
- Forrest, M. D. F1F0 ATP hydrolysis is a determinant of metabolic rate, a correlate of lifespan, and a weakness of cancer. Preprint at bioRxiv https://doi.org/10.1101/2021.10.28.466310 (2022). · DOI
- Ester, M., Kriegel, H.-P., Sander, J. & Xu, X. A. Density-based algorithm for discovering clusters in large spatial databases with noise. kdd 96, 226–231 (1996).
- Crofts, S. J. C., Latorre-Crespo, E. & Chandra, T. DNA methylation rates scale with maximum lifespan across mammals. Preprint at bioRxiv https://doi.org/10.1101/2023.05.15.540689 (2023). · DOI
- Seluanov, A. et al. Telomerase activity coevolves with body mass not lifespan. Aging Cell 6, 45–52 (2007). · DOI
- Buffenstein, R. The naked mole-rat: a new long-living model for human aging research. J. Gerontol. A Biol. Sci. Med. Sci. 60, 1369–1377 (2005). · DOI
- Pfeifer, G. P., Steigerwald, S. D., Hansen, R. S., Gartler, S. M. & Riggs, A. D. Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability. Proc. Natl Acad. Sci. USA 87, 8252–8256 (1990). · DOI
- Dabrowski, J. K. et al. Probabilistic inference of epigenetic age acceleration from cellular dynamics. Preprint at bioRxiv https://doi.org/10.1101/2023.03.01.530570 (2023). · DOI
- Olova, N., Simpson, D. J., Marioni, R. E. & Chandra, T. Partial reprogramming induces a steady decline in epigenetic age before loss of somatic identity. Aging Cell 18, e12877 (2019). · DOI · Paper page
- Horvath, S. & Raj, K. DNA methylation-based biomarkers and the epigenetic clock theory of ageing. Nat. Rev. Genet. 19, 371–384 (2018). · DOI · Paper page
- Dingli, D., Traulsen, A. & Pacheco, J. M. Dynamics of haemopoiesis across mammals. Proc. Biol. Sci. 275, 2389–2392 (2008).
- Tacutu, R. et al. Human ageing genomic resources: new and updated databases. Nucleic Acids Res. 46, D1083–D1090 (2018). · DOI · Paper page
- Guevara, E. E. et al. Age-associated epigenetic change in chimpanzees and humans. Philos. Trans. R. Soc. Lond. B Biol. Sci. 375, 20190616 (2020). · DOI
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A damage accumulation model identifies distinct aging regimes across species
Raz, N., Yang, Y., Pridham, G., Shenhar, B., Frenkel, S., Levy, T., Tlusty, T., Mayo, A., & Alon, U. (2026) · Nature Aging · doi:10.1038/s43587-026-01138-7 · Cited by 7
Metadata
- Authors
- Crofts, S. J. C., Latorre-Crespo, E., & Chandra, T.
- Venue
- Nature Aging
- Published
- 2023-12-04
- Volume
- 4
- Issue
- 1
- Pages
- 27-32
- ISSN
- 2662-8465
- PMC
- PMC10798888
- Cited by
- 28
- References
- 5
- Language
- en
- Funders
- RCUK | Medical Research Council (MC_UU_00009/2)
- University of Edinburgh
- T.C. is supported through a Chancellor’s Fellow at the University of Edinburgh and the MRC Human Genetics Unit.
- Wellcome Trust (grant.226831/Z/22/Z)
- E.L.C. is a cross-disciplinary postdoctoral fellow supported by funding from the University of Edinburgh and the Medical Research Council
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