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Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation

AIM: To investigate the effect of a protein restriction and a supplementation with methyl donor nutrients during fetal and early postnatal life on the expression and epigenetic state of imprinted genes from the IGF system. MATERIALS & METHODS: Pregnant female rats were fed a protein-restricted d...

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Autores principales: Amarger, Valérie, Giudicelli, Fanny, Pagniez, Anthony, Parnet, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351714/
https://www.ncbi.nlm.nih.gov/pubmed/28344827
http://dx.doi.org/10.4155/fsoa-2016-0077
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author Amarger, Valérie
Giudicelli, Fanny
Pagniez, Anthony
Parnet, Patricia
author_facet Amarger, Valérie
Giudicelli, Fanny
Pagniez, Anthony
Parnet, Patricia
author_sort Amarger, Valérie
collection PubMed
description AIM: To investigate the effect of a protein restriction and a supplementation with methyl donor nutrients during fetal and early postnatal life on the expression and epigenetic state of imprinted genes from the IGF system. MATERIALS & METHODS: Pregnant female rats were fed a protein-restricted diet supplemented or not with methyl donor. RESULTS: Gene expression of the Igf2, H19, Igf1, Igf2r and Plagl1 genes in the liver of male offspring at birth and weaning was strongly influenced by maternal diet. Whereas the methylation profiles of the Igf2, H19 and Igf2r genes were remarkably stable, DNA methylation of Plagl1 promoter was slightly modified. CONCLUSION: DNA methylation of most, but not all, imprinted gene regulatory regions was resistant to methyl group nutritional supply.
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spelling pubmed-53517142017-03-24 Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation Amarger, Valérie Giudicelli, Fanny Pagniez, Anthony Parnet, Patricia Future Sci OA Research Article AIM: To investigate the effect of a protein restriction and a supplementation with methyl donor nutrients during fetal and early postnatal life on the expression and epigenetic state of imprinted genes from the IGF system. MATERIALS & METHODS: Pregnant female rats were fed a protein-restricted diet supplemented or not with methyl donor. RESULTS: Gene expression of the Igf2, H19, Igf1, Igf2r and Plagl1 genes in the liver of male offspring at birth and weaning was strongly influenced by maternal diet. Whereas the methylation profiles of the Igf2, H19 and Igf2r genes were remarkably stable, DNA methylation of Plagl1 promoter was slightly modified. CONCLUSION: DNA methylation of most, but not all, imprinted gene regulatory regions was resistant to methyl group nutritional supply. Future Science Ltd 2016-12-13 /pmc/articles/PMC5351714/ /pubmed/28344827 http://dx.doi.org/10.4155/fsoa-2016-0077 Text en © Valerie Amarger This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Amarger, Valérie
Giudicelli, Fanny
Pagniez, Anthony
Parnet, Patricia
Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title_full Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title_fullStr Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title_full_unstemmed Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title_short Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation
title_sort perinatal high methyl donor alters gene expression in igf system in male offspring without altering dna methylation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351714/
https://www.ncbi.nlm.nih.gov/pubmed/28344827
http://dx.doi.org/10.4155/fsoa-2016-0077
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