Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid

A large body of evidence from human and animal studies demonstrates that the maternal diet during pregnancy can programme physiological and metabolic functions in the developing fetus, effectively determining susceptibility to later disease. The mechanistic basis of such programming is unclear but m...

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Main Authors: Altobelli, Gioia, Bogdarina, Irina, Stupka, Elia, Clark, Adrian J.C., Langley-Evans, Simon C.
Format: Article
Published: Public Library of Science 2013
Online Access:https://eprints.nottingham.ac.uk/28473/
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author Altobelli, Gioia
Bogdarina, Irina
Stupka, Elia
Clark, Adrian J.C.
Langley-Evans, Simon C.
author_facet Altobelli, Gioia
Bogdarina, Irina
Stupka, Elia
Clark, Adrian J.C.
Langley-Evans, Simon C.
author_sort Altobelli, Gioia
building Nottingham Research Data Repository
collection Online Access
description A large body of evidence from human and animal studies demonstrates that the maternal diet during pregnancy can programme physiological and metabolic functions in the developing fetus, effectively determining susceptibility to later disease. The mechanistic basis of such programming is unclear but may involve resetting of epigenetic marks and fetal gene expression. The aim of this study was to evaluate genome-wide DNA methylation and gene expression in the livers of newborn rats exposed to maternal protein restriction. On day one postnatally, there were 618 differentially expressed genes and 1183 differentially methylated regions (FDR 5%). The functional analysis of differentially expressed genes indicated a significant effect on DNA repair/cycle/maintenance functions and of lipid, amino acid metabolism and circadian functions. Enrichment for known biological functions was found to be associated with differentially methylated regions. Moreover, these epigenetically altered regions overlapped genetic loci associated with metabolic and cardiovascular diseases. Both expression changes and DNA methylation changes were largely reversed by supplementing the protein restricted diet with folic acid. Although the epigenetic and gene expression signatures appeared to underpin largely different biological processes, the gene expression profile of DNA methyl transferases was altered, providing a potential link between the two molecular signatures. The data showed that maternal protein restriction is associated with widespread differential gene expression and DNA methylation across the genome, and that folic acid is able to reset both molecular signatures.
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spelling nottingham-284732020-05-04T16:40:26Z https://eprints.nottingham.ac.uk/28473/ Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid Altobelli, Gioia Bogdarina, Irina Stupka, Elia Clark, Adrian J.C. Langley-Evans, Simon C. A large body of evidence from human and animal studies demonstrates that the maternal diet during pregnancy can programme physiological and metabolic functions in the developing fetus, effectively determining susceptibility to later disease. The mechanistic basis of such programming is unclear but may involve resetting of epigenetic marks and fetal gene expression. The aim of this study was to evaluate genome-wide DNA methylation and gene expression in the livers of newborn rats exposed to maternal protein restriction. On day one postnatally, there were 618 differentially expressed genes and 1183 differentially methylated regions (FDR 5%). The functional analysis of differentially expressed genes indicated a significant effect on DNA repair/cycle/maintenance functions and of lipid, amino acid metabolism and circadian functions. Enrichment for known biological functions was found to be associated with differentially methylated regions. Moreover, these epigenetically altered regions overlapped genetic loci associated with metabolic and cardiovascular diseases. Both expression changes and DNA methylation changes were largely reversed by supplementing the protein restricted diet with folic acid. Although the epigenetic and gene expression signatures appeared to underpin largely different biological processes, the gene expression profile of DNA methyl transferases was altered, providing a potential link between the two molecular signatures. The data showed that maternal protein restriction is associated with widespread differential gene expression and DNA methylation across the genome, and that folic acid is able to reset both molecular signatures. Public Library of Science 2013-12-31 Article PeerReviewed Altobelli, Gioia, Bogdarina, Irina, Stupka, Elia, Clark, Adrian J.C. and Langley-Evans, Simon C. (2013) Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid. PlosOne, 8 . e82989/1-e82989/11. ISSN 1932-6203 http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0082989 doi:10.1371/journal.pone.0082989 doi:10.1371/journal.pone.0082989
spellingShingle Altobelli, Gioia
Bogdarina, Irina
Stupka, Elia
Clark, Adrian J.C.
Langley-Evans, Simon C.
Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title_full Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title_fullStr Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title_full_unstemmed Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title_short Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
title_sort genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid
url https://eprints.nottingham.ac.uk/28473/
https://eprints.nottingham.ac.uk/28473/
https://eprints.nottingham.ac.uk/28473/