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Maternal diet induces persistent DNA methylation changes in the muscle of beef calves

Maternal nutrition during pregnancy can induce epigenetic alterations in the fetal genome, such as changes in DNA methylation. It remains unclear whether these epigenetic alterations due to changes in maternal nutrition are transitory or persist over time. Here, we hypothesized that maternal methion...

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Autores principales: Amorín, Rocío, Liu, Lihe, Moriel, Philipe, DiLorenzo, Nicolás, Lancaster, Phillip A., Peñagaricano, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884291/
https://www.ncbi.nlm.nih.gov/pubmed/36709351
http://dx.doi.org/10.1038/s41598-023-28896-3
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author Amorín, Rocío
Liu, Lihe
Moriel, Philipe
DiLorenzo, Nicolás
Lancaster, Phillip A.
Peñagaricano, Francisco
author_facet Amorín, Rocío
Liu, Lihe
Moriel, Philipe
DiLorenzo, Nicolás
Lancaster, Phillip A.
Peñagaricano, Francisco
author_sort Amorín, Rocío
collection PubMed
description Maternal nutrition during pregnancy can induce epigenetic alterations in the fetal genome, such as changes in DNA methylation. It remains unclear whether these epigenetic alterations due to changes in maternal nutrition are transitory or persist over time. Here, we hypothesized that maternal methionine supplementation during preconception and early pregnancy could alter the fetal epigenome, and some of these alterations could persist throughout different developmental stages of the offspring. Beef cows were randomly assigned to either a control or a methionine-rich diet from − 30 to + 90 d, relative to the beginning of the breeding season. The methylome of loin muscle from the same bull calves (n = 10 per maternal diet) at 30 and 200 days of age were evaluated using whole-genome bisulfite sequencing. Notably, a total of 28,310 cytosines showed persistent methylation differences over time between maternal diets (q-value < 0.10, methylation change > 20%). These differentially methylated cytosines were in the transcription start sites, exons, or splice sites of 341 annotated genes. Over-representation analysis revealed that these differentially methylated genes are involved in muscle contraction, DNA and histone methylation, mitochondrial function, reactive oxygen species homeostasis, autophagy, and PI3K signaling pathway, among other functions. In addition, some of the persistently, differentially methylated cytosines were found in CpG islands upstream of genes implicated in mitochondrial activities and immune response. Overall, our study provides evidence that a maternal methionine-rich diet altered fetal epigenome, and some of these epigenetic changes persisted over time.
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spelling pubmed-98842912023-01-30 Maternal diet induces persistent DNA methylation changes in the muscle of beef calves Amorín, Rocío Liu, Lihe Moriel, Philipe DiLorenzo, Nicolás Lancaster, Phillip A. Peñagaricano, Francisco Sci Rep Article Maternal nutrition during pregnancy can induce epigenetic alterations in the fetal genome, such as changes in DNA methylation. It remains unclear whether these epigenetic alterations due to changes in maternal nutrition are transitory or persist over time. Here, we hypothesized that maternal methionine supplementation during preconception and early pregnancy could alter the fetal epigenome, and some of these alterations could persist throughout different developmental stages of the offspring. Beef cows were randomly assigned to either a control or a methionine-rich diet from − 30 to + 90 d, relative to the beginning of the breeding season. The methylome of loin muscle from the same bull calves (n = 10 per maternal diet) at 30 and 200 days of age were evaluated using whole-genome bisulfite sequencing. Notably, a total of 28,310 cytosines showed persistent methylation differences over time between maternal diets (q-value < 0.10, methylation change > 20%). These differentially methylated cytosines were in the transcription start sites, exons, or splice sites of 341 annotated genes. Over-representation analysis revealed that these differentially methylated genes are involved in muscle contraction, DNA and histone methylation, mitochondrial function, reactive oxygen species homeostasis, autophagy, and PI3K signaling pathway, among other functions. In addition, some of the persistently, differentially methylated cytosines were found in CpG islands upstream of genes implicated in mitochondrial activities and immune response. Overall, our study provides evidence that a maternal methionine-rich diet altered fetal epigenome, and some of these epigenetic changes persisted over time. Nature Publishing Group UK 2023-01-28 /pmc/articles/PMC9884291/ /pubmed/36709351 http://dx.doi.org/10.1038/s41598-023-28896-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Amorín, Rocío
Liu, Lihe
Moriel, Philipe
DiLorenzo, Nicolás
Lancaster, Phillip A.
Peñagaricano, Francisco
Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title_full Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title_fullStr Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title_full_unstemmed Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title_short Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
title_sort maternal diet induces persistent dna methylation changes in the muscle of beef calves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884291/
https://www.ncbi.nlm.nih.gov/pubmed/36709351
http://dx.doi.org/10.1038/s41598-023-28896-3
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