Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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
_version_ 1783541626582335488
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
work_keys_str_mv AT mooresarahrose distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT humphreyskathrynleigh distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT colichnatalielisanne distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT daviselenagoetz distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT lindavidtseshen distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT macisaacjulialynn distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT kobormichaelsteffen distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty
AT gotlibianhenry distinctionsbetweensexandtimeinpatternsofdnamethylationacrosspuberty