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Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development

Circular RNAs (circRNAs) have been recognized as critical regulators of skeletal muscle development. Myocyte enhancer factor 2A (MEF2A) is an evolutionarily conserved transcriptional factor that regulates myogenesis. However, it remains unclear whether MEF2A produces functional circRNAs. In this stu...

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Autores principales: Shen, Xiaoxu, Zhao, Xiyu, He, Haorong, Zhao, Jing, Wei, Yuanhang, Chen, Yuqi, Han, Shunshun, Zhu, Yifeng, Zhang, Yao, Zhu, Qing, Yin, Huadong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508632/
https://www.ncbi.nlm.nih.gov/pubmed/37676887
http://dx.doi.org/10.1371/journal.pgen.1010923
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author Shen, Xiaoxu
Zhao, Xiyu
He, Haorong
Zhao, Jing
Wei, Yuanhang
Chen, Yuqi
Han, Shunshun
Zhu, Yifeng
Zhang, Yao
Zhu, Qing
Yin, Huadong
author_facet Shen, Xiaoxu
Zhao, Xiyu
He, Haorong
Zhao, Jing
Wei, Yuanhang
Chen, Yuqi
Han, Shunshun
Zhu, Yifeng
Zhang, Yao
Zhu, Qing
Yin, Huadong
author_sort Shen, Xiaoxu
collection PubMed
description Circular RNAs (circRNAs) have been recognized as critical regulators of skeletal muscle development. Myocyte enhancer factor 2A (MEF2A) is an evolutionarily conserved transcriptional factor that regulates myogenesis. However, it remains unclear whether MEF2A produces functional circRNAs. In this study, we identified two evolutionarily conserved circular MEF2A RNAs (circMEF2As), namely circMEF2A1 and circMEF2A2, in chicken and mouse muscle stem cells. Our findings revealed that circMEF2A1 promotes myogenesis by regulating the miR-30a-3p/PPP3CA/NFATC1 axis, whereas circMEF2A2 facilitates myogenic differentiation by targeting the miR-148a-5p/SLIT3/ROBO2/β-catenin signaling pathway. Furthermore, in vivo experiments demonstrated that circMEF2As both promote skeletal muscle growth. We also discovered that the linear MEF2A mRNA-derived MEF2A protein binds to its own promoter region, accelerating the transcription of MEF2A and upregulating the expression of both linear MEF2A and circMEF2As, forming a MEF2A autoregulated positive feedback loop. Moreover, circMEF2As positively regulate the expression of linear MEF2A by adsorbing miR-30a-3p and miR-148a-5p, which directly contribute to the MEF2A autoregulated feedback loop. Importantly, we found that mouse circMEF2As are essential for the myogenic differentiation of C2C12 cells. Collectively, our results demonstrated the evolution, function, and underlying mechanisms of circMEF2As in animal myogenesis, which may provide novel insight for both the farm animal meat industry and human medicine.
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spelling pubmed-105086322023-09-20 Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development Shen, Xiaoxu Zhao, Xiyu He, Haorong Zhao, Jing Wei, Yuanhang Chen, Yuqi Han, Shunshun Zhu, Yifeng Zhang, Yao Zhu, Qing Yin, Huadong PLoS Genet Research Article Circular RNAs (circRNAs) have been recognized as critical regulators of skeletal muscle development. Myocyte enhancer factor 2A (MEF2A) is an evolutionarily conserved transcriptional factor that regulates myogenesis. However, it remains unclear whether MEF2A produces functional circRNAs. In this study, we identified two evolutionarily conserved circular MEF2A RNAs (circMEF2As), namely circMEF2A1 and circMEF2A2, in chicken and mouse muscle stem cells. Our findings revealed that circMEF2A1 promotes myogenesis by regulating the miR-30a-3p/PPP3CA/NFATC1 axis, whereas circMEF2A2 facilitates myogenic differentiation by targeting the miR-148a-5p/SLIT3/ROBO2/β-catenin signaling pathway. Furthermore, in vivo experiments demonstrated that circMEF2As both promote skeletal muscle growth. We also discovered that the linear MEF2A mRNA-derived MEF2A protein binds to its own promoter region, accelerating the transcription of MEF2A and upregulating the expression of both linear MEF2A and circMEF2As, forming a MEF2A autoregulated positive feedback loop. Moreover, circMEF2As positively regulate the expression of linear MEF2A by adsorbing miR-30a-3p and miR-148a-5p, which directly contribute to the MEF2A autoregulated feedback loop. Importantly, we found that mouse circMEF2As are essential for the myogenic differentiation of C2C12 cells. Collectively, our results demonstrated the evolution, function, and underlying mechanisms of circMEF2As in animal myogenesis, which may provide novel insight for both the farm animal meat industry and human medicine. Public Library of Science 2023-09-07 /pmc/articles/PMC10508632/ /pubmed/37676887 http://dx.doi.org/10.1371/journal.pgen.1010923 Text en © 2023 Shen et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shen, Xiaoxu
Zhao, Xiyu
He, Haorong
Zhao, Jing
Wei, Yuanhang
Chen, Yuqi
Han, Shunshun
Zhu, Yifeng
Zhang, Yao
Zhu, Qing
Yin, Huadong
Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title_full Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title_fullStr Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title_full_unstemmed Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title_short Evolutionary conserved circular MEF2A RNAs regulate myogenic differentiation and skeletal muscle development
title_sort evolutionary conserved circular mef2a rnas regulate myogenic differentiation and skeletal muscle development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508632/
https://www.ncbi.nlm.nih.gov/pubmed/37676887
http://dx.doi.org/10.1371/journal.pgen.1010923
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