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Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development
Functional cells in embryonic myogenesis and postnatal muscle development undergo multiple stages of proliferation and differentiation, which are strict procedural regulation processes. N(6)-methyladenosine (m(6)A) is the most abundant RNA modification that regulates gene expression in specific cell...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389409/ https://www.ncbi.nlm.nih.gov/pubmed/35990615 http://dx.doi.org/10.3389/fcell.2022.929183 |
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author | Yu, Baojun Liu, Jiamin Zhang, Juan Mu, Tong Feng, Xiaofang Ma, Ruoshuang Gu, Yaling |
author_facet | Yu, Baojun Liu, Jiamin Zhang, Juan Mu, Tong Feng, Xiaofang Ma, Ruoshuang Gu, Yaling |
author_sort | Yu, Baojun |
collection | PubMed |
description | Functional cells in embryonic myogenesis and postnatal muscle development undergo multiple stages of proliferation and differentiation, which are strict procedural regulation processes. N(6)-methyladenosine (m(6)A) is the most abundant RNA modification that regulates gene expression in specific cell types in eukaryotes and regulates various biological activities, such as RNA processing and metabolism. Recent studies have shown that m(6)A modification-mediated transcriptional and post-transcriptional regulation plays an essential role in myogenesis. This review outlines embryonic and postnatal myogenic differentiation and summarizes the important roles played by functional cells in each developmental period. Furthermore, the key roles of m(6)A modifications and their regulators in myogenesis were highlighted, and the synergistic regulation of m(6)A modifications with myogenic transcription factors was emphasized to characterize the cascade of transcriptional and post-transcriptional regulation during myogenesis. This review also discusses the crosstalk between m(6)A modifications and non-coding RNAs, proposing a novel mechanism for post-transcriptional regulation during skeletal muscle development. In summary, the transcriptional and post-transcriptional regulatory mechanisms mediated by m(6)A and their regulators may help develop new strategies to maintain muscle homeostasis, which are expected to become targets for animal muscle-specific trait breeding and treatment of muscle metabolic diseases. |
format | Online Article Text |
id | pubmed-9389409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93894092022-08-20 Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development Yu, Baojun Liu, Jiamin Zhang, Juan Mu, Tong Feng, Xiaofang Ma, Ruoshuang Gu, Yaling Front Cell Dev Biol Cell and Developmental Biology Functional cells in embryonic myogenesis and postnatal muscle development undergo multiple stages of proliferation and differentiation, which are strict procedural regulation processes. N(6)-methyladenosine (m(6)A) is the most abundant RNA modification that regulates gene expression in specific cell types in eukaryotes and regulates various biological activities, such as RNA processing and metabolism. Recent studies have shown that m(6)A modification-mediated transcriptional and post-transcriptional regulation plays an essential role in myogenesis. This review outlines embryonic and postnatal myogenic differentiation and summarizes the important roles played by functional cells in each developmental period. Furthermore, the key roles of m(6)A modifications and their regulators in myogenesis were highlighted, and the synergistic regulation of m(6)A modifications with myogenic transcription factors was emphasized to characterize the cascade of transcriptional and post-transcriptional regulation during myogenesis. This review also discusses the crosstalk between m(6)A modifications and non-coding RNAs, proposing a novel mechanism for post-transcriptional regulation during skeletal muscle development. In summary, the transcriptional and post-transcriptional regulatory mechanisms mediated by m(6)A and their regulators may help develop new strategies to maintain muscle homeostasis, which are expected to become targets for animal muscle-specific trait breeding and treatment of muscle metabolic diseases. Frontiers Media S.A. 2022-08-05 /pmc/articles/PMC9389409/ /pubmed/35990615 http://dx.doi.org/10.3389/fcell.2022.929183 Text en Copyright © 2022 Yu, Liu, Zhang, Mu, Feng, Ma and Gu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Yu, Baojun Liu, Jiamin Zhang, Juan Mu, Tong Feng, Xiaofang Ma, Ruoshuang Gu, Yaling Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title | Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title_full | Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title_fullStr | Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title_full_unstemmed | Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title_short | Regulatory role of RNA N(6)-methyladenosine modifications during skeletal muscle development |
title_sort | regulatory role of rna n(6)-methyladenosine modifications during skeletal muscle development |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389409/ https://www.ncbi.nlm.nih.gov/pubmed/35990615 http://dx.doi.org/10.3389/fcell.2022.929183 |
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