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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...

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Detalles Bibliográficos
Autores principales: Yu, Baojun, Liu, Jiamin, Zhang, Juan, Mu, Tong, Feng, Xiaofang, Ma, Ruoshuang, Gu, Yaling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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
Descripción
Sumario: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.