bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene

miR-23a, a member of the miR-23a/24-2/27a cluster, has been demonstrated to play pivotal roles in many cellular activities. However, the mechanisms of how bta-miR-23a controls the myogenic differentiation (MD) of PDGFRα<sup>−</sup> bovine progenitor cells (bPCs) remain poorly understood....

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Main Authors: Xin Hu, Yishen Xing, Ling Ren, Yahui Wang, Qian Li, Qiyuan Yang, Min Du, Lingyang Xu, Luc Willems, Junya Li, Lupei Zhang
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/11/10/1232
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author Xin Hu
Yishen Xing
Ling Ren
Yahui Wang
Qian Li
Qiyuan Yang
Min Du
Lingyang Xu
Luc Willems
Junya Li
Lupei Zhang
author_facet Xin Hu
Yishen Xing
Ling Ren
Yahui Wang
Qian Li
Qiyuan Yang
Min Du
Lingyang Xu
Luc Willems
Junya Li
Lupei Zhang
author_sort Xin Hu
collection DOAJ
description miR-23a, a member of the miR-23a/24-2/27a cluster, has been demonstrated to play pivotal roles in many cellular activities. However, the mechanisms of how bta-miR-23a controls the myogenic differentiation (MD) of PDGFRα<sup>−</sup> bovine progenitor cells (bPCs) remain poorly understood. In the present work, bta-miR-23a expression was increased during the MD of <sup>PDGFRα−</sup> bPCs. Moreover, bta-miR-23a overexpression significantly promoted the MD of <sup>PDGFRα−</sup> bPCs. Luciferase reporter assays showed that the 3’-UTR region of <i>MDFIC</i> (MyoD family inhibitor domain containing) could be a promising target of bta-miR-23a, which resulted in its post-transcriptional down-regulation. Additionally, the knockdown of <i>MDFIC</i> by siRNA facilitated the MD of <sup>PDGFRα−</sup> bPCs, while the overexpression of <i>MDFIC</i> inhibited the activating effect of bta-miR-23a during MD. Of note, <i>MDFIC</i> might function through the interaction between <i>MyoG</i> transcription factor and <i>MEF2C</i> promoter. This study reveals that bta-miR-23a can promote the MD of <sup>PDGFRα−</sup> bPCs through post-transcriptional downregulation of <i>MDFIC</i>.
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spelling doaj.art-220e5abc410c4cc4b6a038def039df3f2023-11-20T17:50:10ZengMDPI AGGenes2073-44252020-10-011110123210.3390/genes11101232bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> GeneXin Hu0Yishen Xing1Ling Ren2Yahui Wang3Qian Li4Qiyuan Yang5Min Du6Lingyang Xu7Luc Willems8Junya Li9Lupei Zhang10Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01655, USAWashington Center for Muscle Biology and Department of Animal Sciences, Washington State University, Pullman, WA 99164, USAInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaMolecular and Cellular Biology, Gembloux Agro-Bio Tech, University of Liège, 5030 Gembloux, BelgiumInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinaInstitute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, ChinamiR-23a, a member of the miR-23a/24-2/27a cluster, has been demonstrated to play pivotal roles in many cellular activities. However, the mechanisms of how bta-miR-23a controls the myogenic differentiation (MD) of PDGFRα<sup>−</sup> bovine progenitor cells (bPCs) remain poorly understood. In the present work, bta-miR-23a expression was increased during the MD of <sup>PDGFRα−</sup> bPCs. Moreover, bta-miR-23a overexpression significantly promoted the MD of <sup>PDGFRα−</sup> bPCs. Luciferase reporter assays showed that the 3’-UTR region of <i>MDFIC</i> (MyoD family inhibitor domain containing) could be a promising target of bta-miR-23a, which resulted in its post-transcriptional down-regulation. Additionally, the knockdown of <i>MDFIC</i> by siRNA facilitated the MD of <sup>PDGFRα−</sup> bPCs, while the overexpression of <i>MDFIC</i> inhibited the activating effect of bta-miR-23a during MD. Of note, <i>MDFIC</i> might function through the interaction between <i>MyoG</i> transcription factor and <i>MEF2C</i> promoter. This study reveals that bta-miR-23a can promote the MD of <sup>PDGFRα−</sup> bPCs through post-transcriptional downregulation of <i>MDFIC</i>.https://www.mdpi.com/2073-4425/11/10/1232bta-miR-23afetal muscle development<i>MDFIC</i>
spellingShingle Xin Hu
Yishen Xing
Ling Ren
Yahui Wang
Qian Li
Qiyuan Yang
Min Du
Lingyang Xu
Luc Willems
Junya Li
Lupei Zhang
bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
Genes
bta-miR-23a
fetal muscle development
<i>MDFIC</i>
title bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
title_full bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
title_fullStr bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
title_full_unstemmed bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
title_short bta-miR-23a Regulates the Myogenic Differentiation of Fetal Bovine Skeletal Muscle-Derived Progenitor Cells by Targeting <i>MDFIC</i> Gene
title_sort bta mir 23a regulates the myogenic differentiation of fetal bovine skeletal muscle derived progenitor cells by targeting i mdfic i gene
topic bta-miR-23a
fetal muscle development
<i>MDFIC</i>
url https://www.mdpi.com/2073-4425/11/10/1232
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