Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy

Prior DNA methylation (DNA-m) analyses have identified cytosine-phosphate-guanine (CpG) sites, which show either a significant change or consistency during lifetime. However, the proportion of CpGs that are neither significantly different nor consistent over time (indifferent CpGs) is unknown. We in...

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Main Authors: Su Chen, Nandini Mukherjee, Vimala Devi Janjanam, S Hasan Arshad, Ramesh J Kurukulaaratchy, John W Holloway, Hongmei Zhang, Wilfried Karmaus
Format: Article
Language:English
Published: SAGE Publishing 2017-07-01
Series:Genetics and Epigenetics
Online Access:https://dx.doi.org/10.1177/1179237X17721540
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spelling doaj-22f9db3ab62f439eafc2e52d84883f9b2020-11-24T21:04:32ZengSAGE PublishingGenetics and Epigenetics1179-237X2017-07-01910.1177/1179237X17721540Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and PregnancySu Chen0Nandini Mukherjee1Vimala Devi Janjanam2S Hasan Arshad3Ramesh J Kurukulaaratchy4John W Holloway5Hongmei Zhang6Wilfried Karmaus7Department of Mathematical Sciences, The University of Memphis, Memphis, TN, USADivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, The University of Memphis, Memphis, TN, USADivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, The University of Memphis, Memphis, TN, USAThe David Hide Asthma and Allergy Research Centre, Newport, UKThe David Hide Asthma and Allergy Research Centre, Newport, UKAcademic Unit of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, UKDivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, The University of Memphis, Memphis, TN, USADivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, The University of Memphis, Memphis, TN, USAPrior DNA methylation (DNA-m) analyses have identified cytosine-phosphate-guanine (CpG) sites, which show either a significant change or consistency during lifetime. However, the proportion of CpGs that are neither significantly different nor consistent over time (indifferent CpGs) is unknown. We investigated the methylation dynamics, both longitudinal changes and consistency, in women from preadolescence to late pregnancy using DNA-m of peripheral blood cells. Consistency of cell type–adjusted DNA-m between paired individuals was assessed by regressing CpGs of subsequent age on the prior, stability by intraclass correlation coefficients (>0.5), and changes by linear mixed models. In the first 2 transitions (10-18 years and 18 years to early pregnancy), 19.5% and 20.9% CpGs were consistent, but only 0.35% in the third transition (from early to late pregnancy). Significant changes in methylation were found in 0.7%, 5.6%, and 0% CpGs, respectively. Functional enrichment analyses of genes with significant changes in DNA-m in early pregnancy (5.6%) showed that the maternal DNA-m seems to reflect signaling pathways between the uterus and the trophoblast. The transition from early to late pregnancy showed low consistency/stability and no changes, suggesting the presence of a large proportion of indifferent CpGs in late pregnancy.https://dx.doi.org/10.1177/1179237X17721540
collection DOAJ
language English
format Article
sources DOAJ
author Su Chen
Nandini Mukherjee
Vimala Devi Janjanam
S Hasan Arshad
Ramesh J Kurukulaaratchy
John W Holloway
Hongmei Zhang
Wilfried Karmaus
spellingShingle Su Chen
Nandini Mukherjee
Vimala Devi Janjanam
S Hasan Arshad
Ramesh J Kurukulaaratchy
John W Holloway
Hongmei Zhang
Wilfried Karmaus
Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
Genetics and Epigenetics
author_facet Su Chen
Nandini Mukherjee
Vimala Devi Janjanam
S Hasan Arshad
Ramesh J Kurukulaaratchy
John W Holloway
Hongmei Zhang
Wilfried Karmaus
author_sort Su Chen
title Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
title_short Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
title_full Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
title_fullStr Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
title_full_unstemmed Consistency and Variability of DNA Methylation in Women During Puberty, Young Adulthood, and Pregnancy
title_sort consistency and variability of dna methylation in women during puberty, young adulthood, and pregnancy
publisher SAGE Publishing
series Genetics and Epigenetics
issn 1179-237X
publishDate 2017-07-01
description Prior DNA methylation (DNA-m) analyses have identified cytosine-phosphate-guanine (CpG) sites, which show either a significant change or consistency during lifetime. However, the proportion of CpGs that are neither significantly different nor consistent over time (indifferent CpGs) is unknown. We investigated the methylation dynamics, both longitudinal changes and consistency, in women from preadolescence to late pregnancy using DNA-m of peripheral blood cells. Consistency of cell type–adjusted DNA-m between paired individuals was assessed by regressing CpGs of subsequent age on the prior, stability by intraclass correlation coefficients (>0.5), and changes by linear mixed models. In the first 2 transitions (10-18 years and 18 years to early pregnancy), 19.5% and 20.9% CpGs were consistent, but only 0.35% in the third transition (from early to late pregnancy). Significant changes in methylation were found in 0.7%, 5.6%, and 0% CpGs, respectively. Functional enrichment analyses of genes with significant changes in DNA-m in early pregnancy (5.6%) showed that the maternal DNA-m seems to reflect signaling pathways between the uterus and the trophoblast. The transition from early to late pregnancy showed low consistency/stability and no changes, suggesting the presence of a large proportion of indifferent CpGs in late pregnancy.
url https://dx.doi.org/10.1177/1179237X17721540
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