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miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene

Skeletal muscle formation is an extremely important step in animal growth and development. Recent studies have found that TMEM8c (also known as Myomaker, MYMK), a muscle-specific transmembrane protein, can promote myoblast fusion and plays a key role in the normal development of skeletal muscle. How...

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Autores principales: Ma, Jideng, Zhu, Yan, Zhou, Xiankun, Zhang, Jinwei, Sun, Jing, Li, Zhengjie, Jin, Long, Long, Keren, Lu, Lu, Ge, Liangpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136817/
https://www.ncbi.nlm.nih.gov/pubmed/37190016
http://dx.doi.org/10.3390/cells12081107
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author Ma, Jideng
Zhu, Yan
Zhou, Xiankun
Zhang, Jinwei
Sun, Jing
Li, Zhengjie
Jin, Long
Long, Keren
Lu, Lu
Ge, Liangpeng
author_facet Ma, Jideng
Zhu, Yan
Zhou, Xiankun
Zhang, Jinwei
Sun, Jing
Li, Zhengjie
Jin, Long
Long, Keren
Lu, Lu
Ge, Liangpeng
author_sort Ma, Jideng
collection PubMed
description Skeletal muscle formation is an extremely important step in animal growth and development. Recent studies have found that TMEM8c (also known as Myomaker, MYMK), a muscle-specific transmembrane protein, can promote myoblast fusion and plays a key role in the normal development of skeletal muscle. However, the effect of Myomaker on porcine (Sus scrofa) myoblast fusion and the underlying regulatory mechanisms remain largely unknown. Therefore, in this study, we focused on the role and corresponding regulatory mechanism of the Myomaker gene during skeletal muscle development, cell differentiation, and muscle injury repair in pigs. We obtained the entire 3′ UTR sequence of porcine Myomaker using the 3′ RACE approach and found that miR-205 inhibited porcine myoblast fusion by targeting the 3′ UTR of Myomaker. In addition, based on a constructed porcine acute muscle injury model, we discovered that both the mRNA and protein expression of Myomaker were activated in the injured muscle, while miR-205 expression was significantly inhibited during skeletal muscle regeneration. The negative regulatory relationship between miR-205 and Myomaker was further confirmed in vivo. Taken together, the present study reveals that Myomaker plays a role during porcine myoblast fusion and skeletal muscle regeneration and demonstrates that miR-205 inhibits myoblast fusion through targeted regulation of the expression of Myomaker.
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spelling pubmed-101368172023-04-28 miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene Ma, Jideng Zhu, Yan Zhou, Xiankun Zhang, Jinwei Sun, Jing Li, Zhengjie Jin, Long Long, Keren Lu, Lu Ge, Liangpeng Cells Article Skeletal muscle formation is an extremely important step in animal growth and development. Recent studies have found that TMEM8c (also known as Myomaker, MYMK), a muscle-specific transmembrane protein, can promote myoblast fusion and plays a key role in the normal development of skeletal muscle. However, the effect of Myomaker on porcine (Sus scrofa) myoblast fusion and the underlying regulatory mechanisms remain largely unknown. Therefore, in this study, we focused on the role and corresponding regulatory mechanism of the Myomaker gene during skeletal muscle development, cell differentiation, and muscle injury repair in pigs. We obtained the entire 3′ UTR sequence of porcine Myomaker using the 3′ RACE approach and found that miR-205 inhibited porcine myoblast fusion by targeting the 3′ UTR of Myomaker. In addition, based on a constructed porcine acute muscle injury model, we discovered that both the mRNA and protein expression of Myomaker were activated in the injured muscle, while miR-205 expression was significantly inhibited during skeletal muscle regeneration. The negative regulatory relationship between miR-205 and Myomaker was further confirmed in vivo. Taken together, the present study reveals that Myomaker plays a role during porcine myoblast fusion and skeletal muscle regeneration and demonstrates that miR-205 inhibits myoblast fusion through targeted regulation of the expression of Myomaker. MDPI 2023-04-07 /pmc/articles/PMC10136817/ /pubmed/37190016 http://dx.doi.org/10.3390/cells12081107 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ma, Jideng
Zhu, Yan
Zhou, Xiankun
Zhang, Jinwei
Sun, Jing
Li, Zhengjie
Jin, Long
Long, Keren
Lu, Lu
Ge, Liangpeng
miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title_full miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title_fullStr miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title_full_unstemmed miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title_short miR-205 Regulates the Fusion of Porcine Myoblast by Targeting the Myomaker Gene
title_sort mir-205 regulates the fusion of porcine myoblast by targeting the myomaker gene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136817/
https://www.ncbi.nlm.nih.gov/pubmed/37190016
http://dx.doi.org/10.3390/cells12081107
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