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Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring

Epigenetic mechanisms have an important role in the pre- and peri-conceptional programming by maternal nutrition. Yet, whether or not RNA m(6)A methylation—an old epigenetic marker receiving increased attention recently—is involved remains an unknown question. In this study, mouse high-fat feeding p...

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Autores principales: Li, Xiao, Yang, Jing, Zhu, Youbo, Liu, Yuan, Shi, Xin’e, Yang, Gongshe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5000733/
https://www.ncbi.nlm.nih.gov/pubmed/27548155
http://dx.doi.org/10.3390/ijms17081336
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author Li, Xiao
Yang, Jing
Zhu, Youbo
Liu, Yuan
Shi, Xin’e
Yang, Gongshe
author_facet Li, Xiao
Yang, Jing
Zhu, Youbo
Liu, Yuan
Shi, Xin’e
Yang, Gongshe
author_sort Li, Xiao
collection PubMed
description Epigenetic mechanisms have an important role in the pre- and peri-conceptional programming by maternal nutrition. Yet, whether or not RNA m(6)A methylation—an old epigenetic marker receiving increased attention recently—is involved remains an unknown question. In this study, mouse high-fat feeding prior to conception was shown to induce overweight and glucose intolerant dams, which then continued to be exposed to a high-fat diet during gestation and lactation. The dams on a standard diet throughout the whole experiment were used as a control. Results showed that maternal high-fat intake impaired postnatal growth in male offspring, indicated by decreased body weight and Lee’s index at 3, 8 and 15 weeks old, but the percentages of visceral fat and tibialis anterior relative to the whole body weights were significantly increased at eight weeks of age. The maternal high-fat exposure significantly increased mRNA N(6)-methyladenosine (m(6)A) levels in visceral fat at three weeks old, combined with downregulated Fat mass and obesity-associated gene (FTO) and upregulated Methyltransferase like 3 (METTL3) transcription, and these changes were reversed at eight weeks of age. In the tibialis anterior muscle, the maternal high-fat diet significantly enhanced m(6)A modifications at three weeks, and lowered m(6)A levels at 15 weeks of age. Accordingly, FTO transcription was significantly inhibited at three weeks and stimulated at 15 weeks of age, and METTL3 transcripts were significantly improved at three weeks. Interestingly, both FTO and METTL3 transcription was significantly elevated at eight weeks of age, and yet the m(6)A modifications remained unchanged. Our study showed that maternal high-fat intake could affect mRNA m(6)A modifications and its related genes in offspring in a tissue-specific and development-dependent way, and provided an interesting indication of the working of the m(6)A system during the transmission from maternal nutrition to subsequent generations.
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spelling pubmed-50007332016-09-01 Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring Li, Xiao Yang, Jing Zhu, Youbo Liu, Yuan Shi, Xin’e Yang, Gongshe Int J Mol Sci Article Epigenetic mechanisms have an important role in the pre- and peri-conceptional programming by maternal nutrition. Yet, whether or not RNA m(6)A methylation—an old epigenetic marker receiving increased attention recently—is involved remains an unknown question. In this study, mouse high-fat feeding prior to conception was shown to induce overweight and glucose intolerant dams, which then continued to be exposed to a high-fat diet during gestation and lactation. The dams on a standard diet throughout the whole experiment were used as a control. Results showed that maternal high-fat intake impaired postnatal growth in male offspring, indicated by decreased body weight and Lee’s index at 3, 8 and 15 weeks old, but the percentages of visceral fat and tibialis anterior relative to the whole body weights were significantly increased at eight weeks of age. The maternal high-fat exposure significantly increased mRNA N(6)-methyladenosine (m(6)A) levels in visceral fat at three weeks old, combined with downregulated Fat mass and obesity-associated gene (FTO) and upregulated Methyltransferase like 3 (METTL3) transcription, and these changes were reversed at eight weeks of age. In the tibialis anterior muscle, the maternal high-fat diet significantly enhanced m(6)A modifications at three weeks, and lowered m(6)A levels at 15 weeks of age. Accordingly, FTO transcription was significantly inhibited at three weeks and stimulated at 15 weeks of age, and METTL3 transcripts were significantly improved at three weeks. Interestingly, both FTO and METTL3 transcription was significantly elevated at eight weeks of age, and yet the m(6)A modifications remained unchanged. Our study showed that maternal high-fat intake could affect mRNA m(6)A modifications and its related genes in offspring in a tissue-specific and development-dependent way, and provided an interesting indication of the working of the m(6)A system during the transmission from maternal nutrition to subsequent generations. MDPI 2016-08-19 /pmc/articles/PMC5000733/ /pubmed/27548155 http://dx.doi.org/10.3390/ijms17081336 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Xiao
Yang, Jing
Zhu, Youbo
Liu, Yuan
Shi, Xin’e
Yang, Gongshe
Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title_full Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title_fullStr Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title_full_unstemmed Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title_short Mouse Maternal High-Fat Intake Dynamically Programmed mRNA m(6)A Modifications in Adipose and Skeletal Muscle Tissues in Offspring
title_sort mouse maternal high-fat intake dynamically programmed mrna m(6)a modifications in adipose and skeletal muscle tissues in offspring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5000733/
https://www.ncbi.nlm.nih.gov/pubmed/27548155
http://dx.doi.org/10.3390/ijms17081336
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