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DNA methylation clocks as a predictor for ageing and age estimation in naked mole-rats, Heterocephalus glaber
Author(s) -
Robert Lowe,
Amy F. Danson,
Vardhman K. Rakyan,
Selin Yildizoglu,
Frédéric Saldmann,
Mélanie Viltard,
Gérard Friedlander,
Chris G. Faulkes
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102892
Subject(s) - ageing , epigenetics , dna methylation , cpg site , methylation , biology , correlation , evolutionary biology , genetics , dna , gene , gene expression , geometry , mathematics
The naked mole-rat, Heterocephalus glaber (NMR), the longest-lived rodent, is of significance and interest in the study of biomarkers for ageing. Recent breakthroughs in this field have revealed 'epigenetic clocks' that are based on the temporal accumulation of DNA methylation at specific genomic sites. Here, we validate the hypothesis of an epigenetic clock in NMRs based on changes in methylation of targeted CpG sites. We initially analysed 51 CpGs in NMR livers spanning an age range of 39-1,144 weeks and found 23 to be significantly associated with age (p<0.05). We then built a predictor of age using these sites. To test the accuracy of this model, we analysed an additional set of liver samples, and were successfully able to predict their age with a root mean squared error of 166 weeks. We also profiled skin samples with the same age range, finding a striking correlation between their predicted age versus their actual age (R=0.93), but which was lower when compared to the liver, suggesting that skin ages slower than the liver in NMRs. Our model will enable the prediction of age in wild-caught and captive NMRs of unknown age, and will be invaluable for further mechanistic studies of mammalian ageing.

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