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Age‐dependent DNA methylation patterns on the Y chromosome in elderly males

The Y chromosome, a sex chromosome that only exists in males, has been ignored in traditional epigenetic association studies for multiple reasons. However, sex differences in aging‐related phenotypes and mortality could suggest a critical role of the sex chromosomes in the aging process. We obtained...

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Autores principales: Lund, Jesper B., Li, Shuxia, Christensen, Kaare, Mengel‐From, Jonas, Soerensen, Mette, Marioni, Riccardo E., Starr, John, Pattie, Alison, Deary, Ian J., Baumbach, Jan, Tan, Qihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996942/
https://www.ncbi.nlm.nih.gov/pubmed/30793472
http://dx.doi.org/10.1111/acel.12907
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author Lund, Jesper B.
Li, Shuxia
Christensen, Kaare
Mengel‐From, Jonas
Soerensen, Mette
Marioni, Riccardo E.
Starr, John
Pattie, Alison
Deary, Ian J.
Baumbach, Jan
Tan, Qihua
author_facet Lund, Jesper B.
Li, Shuxia
Christensen, Kaare
Mengel‐From, Jonas
Soerensen, Mette
Marioni, Riccardo E.
Starr, John
Pattie, Alison
Deary, Ian J.
Baumbach, Jan
Tan, Qihua
author_sort Lund, Jesper B.
collection PubMed
description The Y chromosome, a sex chromosome that only exists in males, has been ignored in traditional epigenetic association studies for multiple reasons. However, sex differences in aging‐related phenotypes and mortality could suggest a critical role of the sex chromosomes in the aging process. We obtained blood‐based DNA methylation data on the Y chromosome for 624 men from four cohorts and performed a chromosome‐wide epigenetic association analysis to detect Y‐linked CpGs differentially methylated over age and cross‐validated the significant CpGs in the four cohorts. We identified 40–219 significant CpG sites (false discovery rate <0.05) with >82% of them hypermethylated with increasing age, which is in strong contrast to the patterns reported on the autosomal chromosomes. Comparing the rate of change in the Y‐linked DNA methylation across cohorts that represent different age intervals revealed a trend of acceleration in DNA methylation with increasing age. The age‐dependent DNA methylation patterns on the Y chromosome were further examined for their association with all‐cause mortality with results suggesting that the predominant pattern of age‐related hypermethylation on the Y chromosome is associated with reduced risk of death.
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spelling pubmed-69969422020-02-05 Age‐dependent DNA methylation patterns on the Y chromosome in elderly males Lund, Jesper B. Li, Shuxia Christensen, Kaare Mengel‐From, Jonas Soerensen, Mette Marioni, Riccardo E. Starr, John Pattie, Alison Deary, Ian J. Baumbach, Jan Tan, Qihua Aging Cell Original Paper The Y chromosome, a sex chromosome that only exists in males, has been ignored in traditional epigenetic association studies for multiple reasons. However, sex differences in aging‐related phenotypes and mortality could suggest a critical role of the sex chromosomes in the aging process. We obtained blood‐based DNA methylation data on the Y chromosome for 624 men from four cohorts and performed a chromosome‐wide epigenetic association analysis to detect Y‐linked CpGs differentially methylated over age and cross‐validated the significant CpGs in the four cohorts. We identified 40–219 significant CpG sites (false discovery rate <0.05) with >82% of them hypermethylated with increasing age, which is in strong contrast to the patterns reported on the autosomal chromosomes. Comparing the rate of change in the Y‐linked DNA methylation across cohorts that represent different age intervals revealed a trend of acceleration in DNA methylation with increasing age. The age‐dependent DNA methylation patterns on the Y chromosome were further examined for their association with all‐cause mortality with results suggesting that the predominant pattern of age‐related hypermethylation on the Y chromosome is associated with reduced risk of death. John Wiley and Sons Inc. 2019-02-21 2020-02 /pmc/articles/PMC6996942/ /pubmed/30793472 http://dx.doi.org/10.1111/acel.12907 Text en © 2019 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Lund, Jesper B.
Li, Shuxia
Christensen, Kaare
Mengel‐From, Jonas
Soerensen, Mette
Marioni, Riccardo E.
Starr, John
Pattie, Alison
Deary, Ian J.
Baumbach, Jan
Tan, Qihua
Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title_full Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title_fullStr Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title_full_unstemmed Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title_short Age‐dependent DNA methylation patterns on the Y chromosome in elderly males
title_sort age‐dependent dna methylation patterns on the y chromosome in elderly males
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996942/
https://www.ncbi.nlm.nih.gov/pubmed/30793472
http://dx.doi.org/10.1111/acel.12907
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