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Distinctions between sex and time in patterns of DNA methylation across puberty
BACKGROUND: There are significant sex differences in human physiology and disease; the genomic sources of these differences, however, are not well understood. During puberty, a drastic neuroendocrine shift signals physical changes resulting in robust sex differences in human physiology. Here, we exp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268482/ https://www.ncbi.nlm.nih.gov/pubmed/32493224 http://dx.doi.org/10.1186/s12864-020-06789-3 |
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author | Moore, Sarah Rose Humphreys, Kathryn Leigh Colich, Natalie Lisanne Davis, Elena Goetz Lin, David Tse Shen MacIsaac, Julia Lynn Kobor, Michael Steffen Gotlib, Ian Henry |
author_facet | Moore, Sarah Rose Humphreys, Kathryn Leigh Colich, Natalie Lisanne Davis, Elena Goetz Lin, David Tse Shen MacIsaac, Julia Lynn Kobor, Michael Steffen Gotlib, Ian Henry |
author_sort | Moore, Sarah Rose |
collection | PubMed |
description | BACKGROUND: There are significant sex differences in human physiology and disease; the genomic sources of these differences, however, are not well understood. During puberty, a drastic neuroendocrine shift signals physical changes resulting in robust sex differences in human physiology. Here, we explore how shifting patterns of DNA methylation may inform these pathways of biological plasticity during the pubertal transition. In this study we analyzed DNA methylation (DNAm) in saliva at two time points across the pubertal transition within the same individuals. Our purpose was to compare two domains of DNAm patterns that may inform processes of sexual differentiation 1) sex related sites, which demonstrated differences between males from females and 2) time related sites in which DNAm shifted significantly between timepoints. We further explored the correlated network structure sex and time related DNAm networks and linked these patterns to pubertal stage, assays of salivary testosterone, a reliable diagnostic of free, unbound hormone that is available to act on target tissues, and overlap with androgen response elements. RESULTS: Sites that differed by biological sex were largely independent of sites that underwent change across puberty. Time-related DNAm sites, but not sex-related sites, formed correlated networks that were associated with pubertal stage. Both time and sex DNAm networks reflected salivary testosterone levels that were enriched for androgen response elements, with sex-related DNAm networks being informative of testosterone levels above and beyond biological sex later in the pubertal transition. CONCLUSIONS: These results inform our understanding of the distinction between sex- and time-related differences in DNAm during the critical period of puberty and highlight a novel linkage between correlated patterns of sex-related DNAm and levels of salivary testosterone. |
format | Online Article Text |
id | pubmed-7268482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72684822020-06-07 Distinctions between sex and time in patterns of DNA methylation across puberty Moore, Sarah Rose Humphreys, Kathryn Leigh Colich, Natalie Lisanne Davis, Elena Goetz Lin, David Tse Shen MacIsaac, Julia Lynn Kobor, Michael Steffen Gotlib, Ian Henry BMC Genomics Research Article BACKGROUND: There are significant sex differences in human physiology and disease; the genomic sources of these differences, however, are not well understood. During puberty, a drastic neuroendocrine shift signals physical changes resulting in robust sex differences in human physiology. Here, we explore how shifting patterns of DNA methylation may inform these pathways of biological plasticity during the pubertal transition. In this study we analyzed DNA methylation (DNAm) in saliva at two time points across the pubertal transition within the same individuals. Our purpose was to compare two domains of DNAm patterns that may inform processes of sexual differentiation 1) sex related sites, which demonstrated differences between males from females and 2) time related sites in which DNAm shifted significantly between timepoints. We further explored the correlated network structure sex and time related DNAm networks and linked these patterns to pubertal stage, assays of salivary testosterone, a reliable diagnostic of free, unbound hormone that is available to act on target tissues, and overlap with androgen response elements. RESULTS: Sites that differed by biological sex were largely independent of sites that underwent change across puberty. Time-related DNAm sites, but not sex-related sites, formed correlated networks that were associated with pubertal stage. Both time and sex DNAm networks reflected salivary testosterone levels that were enriched for androgen response elements, with sex-related DNAm networks being informative of testosterone levels above and beyond biological sex later in the pubertal transition. CONCLUSIONS: These results inform our understanding of the distinction between sex- and time-related differences in DNAm during the critical period of puberty and highlight a novel linkage between correlated patterns of sex-related DNAm and levels of salivary testosterone. BioMed Central 2020-06-03 /pmc/articles/PMC7268482/ /pubmed/32493224 http://dx.doi.org/10.1186/s12864-020-06789-3 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Moore, Sarah Rose Humphreys, Kathryn Leigh Colich, Natalie Lisanne Davis, Elena Goetz Lin, David Tse Shen MacIsaac, Julia Lynn Kobor, Michael Steffen Gotlib, Ian Henry Distinctions between sex and time in patterns of DNA methylation across puberty |
title | Distinctions between sex and time in patterns of DNA methylation across puberty |
title_full | Distinctions between sex and time in patterns of DNA methylation across puberty |
title_fullStr | Distinctions between sex and time in patterns of DNA methylation across puberty |
title_full_unstemmed | Distinctions between sex and time in patterns of DNA methylation across puberty |
title_short | Distinctions between sex and time in patterns of DNA methylation across puberty |
title_sort | distinctions between sex and time in patterns of dna methylation across puberty |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268482/ https://www.ncbi.nlm.nih.gov/pubmed/32493224 http://dx.doi.org/10.1186/s12864-020-06789-3 |
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