Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.

This study examines the relationship between common genetic variation within DNA methyltransferase genes and inter-individual variation in DNA methylation. Eleven polymorphisms spanning DNMT1 and DNMT3B were genotyped. Global and gene specific (IGF2, IGFBP3, ZNT5) DNA methylation was quantified by L...

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Main Authors: Catherine Potter, Jill McKay, Alexandra Groom, Dianne Ford, Lisa Coneyworth, John C Mathers, Caroline L Relton
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3788139?pdf=render
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spelling doaj-45c4ef06a51b402493b1475f4a2e7a002020-11-24T21:48:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7650610.1371/journal.pone.0076506Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.Catherine PotterJill McKayAlexandra GroomDianne FordLisa ConeyworthJohn C MathersCaroline L ReltonThis study examines the relationship between common genetic variation within DNA methyltransferase genes and inter-individual variation in DNA methylation. Eleven polymorphisms spanning DNMT1 and DNMT3B were genotyped. Global and gene specific (IGF2, IGFBP3, ZNT5) DNA methylation was quantified by LUMA and bisulfite Pyrosequencing assays, respectively, in neonatal cord blood and in maternal peripheral blood. Associations between maternal genotype and maternal methylation (n (≈) 333), neonatal genotype and neonatal methylation (n (≈) 454), and maternal genotype and neonatal methylation (n (≈) 137) were assessed. The findings of this study provide some support to the hypothesis that genetic variation in DNA methylating enzymes influence DNA methylation at global and gene-specific levels; however observations were not robust to correction for multiple testing. More comprehensive analysis of the influence of genetic variation on global and site specific DNA methylation is warranted.http://europepmc.org/articles/PMC3788139?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Catherine Potter
Jill McKay
Alexandra Groom
Dianne Ford
Lisa Coneyworth
John C Mathers
Caroline L Relton
spellingShingle Catherine Potter
Jill McKay
Alexandra Groom
Dianne Ford
Lisa Coneyworth
John C Mathers
Caroline L Relton
Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
PLoS ONE
author_facet Catherine Potter
Jill McKay
Alexandra Groom
Dianne Ford
Lisa Coneyworth
John C Mathers
Caroline L Relton
author_sort Catherine Potter
title Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
title_short Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
title_full Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
title_fullStr Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
title_full_unstemmed Influence of DNMT genotype on global and site specific DNA methylation patterns in neonates and pregnant women.
title_sort influence of dnmt genotype on global and site specific dna methylation patterns in neonates and pregnant women.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description This study examines the relationship between common genetic variation within DNA methyltransferase genes and inter-individual variation in DNA methylation. Eleven polymorphisms spanning DNMT1 and DNMT3B were genotyped. Global and gene specific (IGF2, IGFBP3, ZNT5) DNA methylation was quantified by LUMA and bisulfite Pyrosequencing assays, respectively, in neonatal cord blood and in maternal peripheral blood. Associations between maternal genotype and maternal methylation (n (≈) 333), neonatal genotype and neonatal methylation (n (≈) 454), and maternal genotype and neonatal methylation (n (≈) 137) were assessed. The findings of this study provide some support to the hypothesis that genetic variation in DNA methylating enzymes influence DNA methylation at global and gene-specific levels; however observations were not robust to correction for multiple testing. More comprehensive analysis of the influence of genetic variation on global and site specific DNA methylation is warranted.
url http://europepmc.org/articles/PMC3788139?pdf=render
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