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Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans

BACKGROUND: The variation in the rate at which humans age may be rooted in early events acting through the genomic regions that are influenced by such events and subsequently are related to health phenotypes in later life. The parent-of-origin-effect (POE)-regulated methylome includes regions enrich...

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Autores principales: Gao, Chenhao, Amador, Carmen, Walker, Rosie M., Campbell, Archie, Madden, Rebecca A., Adams, Mark J., Bai, Xiaomeng, Liu, Ying, Li, Miaoxin, Hayward, Caroline, Porteous, David J., Shen, Xueyi, Evans, Kathryn L., Haley, Chris S., McIntosh, Andrew M., Navarro, Pau, Zeng, Yanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184337/
https://www.ncbi.nlm.nih.gov/pubmed/37189164
http://dx.doi.org/10.1186/s13059-023-02953-6
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author Gao, Chenhao
Amador, Carmen
Walker, Rosie M.
Campbell, Archie
Madden, Rebecca A.
Adams, Mark J.
Bai, Xiaomeng
Liu, Ying
Li, Miaoxin
Hayward, Caroline
Porteous, David J.
Shen, Xueyi
Evans, Kathryn L.
Haley, Chris S.
McIntosh, Andrew M.
Navarro, Pau
Zeng, Yanni
author_facet Gao, Chenhao
Amador, Carmen
Walker, Rosie M.
Campbell, Archie
Madden, Rebecca A.
Adams, Mark J.
Bai, Xiaomeng
Liu, Ying
Li, Miaoxin
Hayward, Caroline
Porteous, David J.
Shen, Xueyi
Evans, Kathryn L.
Haley, Chris S.
McIntosh, Andrew M.
Navarro, Pau
Zeng, Yanni
author_sort Gao, Chenhao
collection PubMed
description BACKGROUND: The variation in the rate at which humans age may be rooted in early events acting through the genomic regions that are influenced by such events and subsequently are related to health phenotypes in later life. The parent-of-origin-effect (POE)-regulated methylome includes regions enriched for genetically controlled imprinting effects (the typical type of POE) and regions influenced by environmental effects associated with parents (the atypical POE). This part of the methylome is heavily influenced by early events, making it a potential route connecting early exposures, the epigenome, and aging. We aim to test the association of POE-CpGs with early and later exposures and subsequently with health-related phenotypes and adult aging. RESULTS: We perform a phenome-wide association analysis for the POE-influenced methylome using GS:SFHS (N(discovery) = 5087, N(replication) = 4450). We identify and replicate 92 POE-CpG-phenotype associations. Most of the associations are contributed by the POE-CpGs belonging to the atypical class where the most strongly enriched associations are with aging (DNAmTL acceleration), intelligence, and parental (maternal) smoking exposure phenotypes. A proportion of the atypical POE-CpGs form co-methylation networks (modules) which are associated with these phenotypes, with one of the aging-associated modules displaying increased within-module methylation connectivity with age. The atypical POE-CpGs also display high levels of methylation heterogeneity, fast information loss with age, and a strong correlation with CpGs contained within epigenetic clocks. CONCLUSIONS: These results identify the association between the atypical POE-influenced methylome and aging and provide new evidence for the “early development of origin” hypothesis for aging in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02953-6.
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spelling pubmed-101843372023-05-16 Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans Gao, Chenhao Amador, Carmen Walker, Rosie M. Campbell, Archie Madden, Rebecca A. Adams, Mark J. Bai, Xiaomeng Liu, Ying Li, Miaoxin Hayward, Caroline Porteous, David J. Shen, Xueyi Evans, Kathryn L. Haley, Chris S. McIntosh, Andrew M. Navarro, Pau Zeng, Yanni Genome Biol Research BACKGROUND: The variation in the rate at which humans age may be rooted in early events acting through the genomic regions that are influenced by such events and subsequently are related to health phenotypes in later life. The parent-of-origin-effect (POE)-regulated methylome includes regions enriched for genetically controlled imprinting effects (the typical type of POE) and regions influenced by environmental effects associated with parents (the atypical POE). This part of the methylome is heavily influenced by early events, making it a potential route connecting early exposures, the epigenome, and aging. We aim to test the association of POE-CpGs with early and later exposures and subsequently with health-related phenotypes and adult aging. RESULTS: We perform a phenome-wide association analysis for the POE-influenced methylome using GS:SFHS (N(discovery) = 5087, N(replication) = 4450). We identify and replicate 92 POE-CpG-phenotype associations. Most of the associations are contributed by the POE-CpGs belonging to the atypical class where the most strongly enriched associations are with aging (DNAmTL acceleration), intelligence, and parental (maternal) smoking exposure phenotypes. A proportion of the atypical POE-CpGs form co-methylation networks (modules) which are associated with these phenotypes, with one of the aging-associated modules displaying increased within-module methylation connectivity with age. The atypical POE-CpGs also display high levels of methylation heterogeneity, fast information loss with age, and a strong correlation with CpGs contained within epigenetic clocks. CONCLUSIONS: These results identify the association between the atypical POE-influenced methylome and aging and provide new evidence for the “early development of origin” hypothesis for aging in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02953-6. BioMed Central 2023-05-15 /pmc/articles/PMC10184337/ /pubmed/37189164 http://dx.doi.org/10.1186/s13059-023-02953-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gao, Chenhao
Amador, Carmen
Walker, Rosie M.
Campbell, Archie
Madden, Rebecca A.
Adams, Mark J.
Bai, Xiaomeng
Liu, Ying
Li, Miaoxin
Hayward, Caroline
Porteous, David J.
Shen, Xueyi
Evans, Kathryn L.
Haley, Chris S.
McIntosh, Andrew M.
Navarro, Pau
Zeng, Yanni
Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title_full Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title_fullStr Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title_full_unstemmed Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title_short Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
title_sort phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184337/
https://www.ncbi.nlm.nih.gov/pubmed/37189164
http://dx.doi.org/10.1186/s13059-023-02953-6
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