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MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts

The proliferation and differentiation of chicken primary myoblasts (CPMs) play an important role in the development of skeletal muscle. In our previous research, RNA-seq analysis showed that microRNA-7 (miR-7) was relatively highly expressed in the proliferation phase of CPMs, but its expression lev...

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Autores principales: Zhang, Genxi, Chen, Fuxiang, Wu, Pengfei, Li, TingTing, He, Mingliang, Yin, Xuemei, Shi, Huiqiang, Duan, Yanjun, Zhang, Tao, Wang, Jinyu, Xie, Kaizhou, Dai, Guojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530283/
https://www.ncbi.nlm.nih.gov/pubmed/33193566
http://dx.doi.org/10.3389/fgene.2020.00842
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author Zhang, Genxi
Chen, Fuxiang
Wu, Pengfei
Li, TingTing
He, Mingliang
Yin, Xuemei
Shi, Huiqiang
Duan, Yanjun
Zhang, Tao
Wang, Jinyu
Xie, Kaizhou
Dai, Guojun
author_facet Zhang, Genxi
Chen, Fuxiang
Wu, Pengfei
Li, TingTing
He, Mingliang
Yin, Xuemei
Shi, Huiqiang
Duan, Yanjun
Zhang, Tao
Wang, Jinyu
Xie, Kaizhou
Dai, Guojun
author_sort Zhang, Genxi
collection PubMed
description The proliferation and differentiation of chicken primary myoblasts (CPMs) play an important role in the development of skeletal muscle. In our previous research, RNA-seq analysis showed that microRNA-7 (miR-7) was relatively highly expressed in the proliferation phase of CPMs, but its expression level decreased significantly after CPM(S)-induced differentiation. Meanwhile, the mechanism by which the miR-7 regulates the proliferation and differentiation of CPMs is still unknown. In this study, we found that the expression levels of miR-7 and the Krüppel-like factor 4 (KLF4) gene were negatively correlated during the embryonic phase, and in vitro induced differentiation. A dual-luciferase assay and a rescue experiment show that there is a target relationship between miR-7 and the KLF4 gene. Meanwhile, the results show that overexpression of miR-7 inhibited the proliferation and differentiation of CPMs, while inhibition of miR-7 had the opposite effects. Furthermore, overexpression of the KLF4 gene was found to significantly promote the proliferation and differentiation of CPMs. Conversely, inhibition of the KLF4 gene was able to significantly decrease the proliferation and differentiation of CPMs. Our results demonstrate, for the first time, that miR-7 inhibits the proliferation and differentiation of myoblasts by targeting the KLF4 gene in chicken primary myoblasts.
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spelling pubmed-75302832020-11-13 MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts Zhang, Genxi Chen, Fuxiang Wu, Pengfei Li, TingTing He, Mingliang Yin, Xuemei Shi, Huiqiang Duan, Yanjun Zhang, Tao Wang, Jinyu Xie, Kaizhou Dai, Guojun Front Genet Genetics The proliferation and differentiation of chicken primary myoblasts (CPMs) play an important role in the development of skeletal muscle. In our previous research, RNA-seq analysis showed that microRNA-7 (miR-7) was relatively highly expressed in the proliferation phase of CPMs, but its expression level decreased significantly after CPM(S)-induced differentiation. Meanwhile, the mechanism by which the miR-7 regulates the proliferation and differentiation of CPMs is still unknown. In this study, we found that the expression levels of miR-7 and the Krüppel-like factor 4 (KLF4) gene were negatively correlated during the embryonic phase, and in vitro induced differentiation. A dual-luciferase assay and a rescue experiment show that there is a target relationship between miR-7 and the KLF4 gene. Meanwhile, the results show that overexpression of miR-7 inhibited the proliferation and differentiation of CPMs, while inhibition of miR-7 had the opposite effects. Furthermore, overexpression of the KLF4 gene was found to significantly promote the proliferation and differentiation of CPMs. Conversely, inhibition of the KLF4 gene was able to significantly decrease the proliferation and differentiation of CPMs. Our results demonstrate, for the first time, that miR-7 inhibits the proliferation and differentiation of myoblasts by targeting the KLF4 gene in chicken primary myoblasts. Frontiers Media S.A. 2020-09-18 /pmc/articles/PMC7530283/ /pubmed/33193566 http://dx.doi.org/10.3389/fgene.2020.00842 Text en Copyright © 2020 Zhang, Chen, Wu, Li, He, Yin, Shi, Duan, Zhang, Wang, Xie and Dai. http://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 Genetics
Zhang, Genxi
Chen, Fuxiang
Wu, Pengfei
Li, TingTing
He, Mingliang
Yin, Xuemei
Shi, Huiqiang
Duan, Yanjun
Zhang, Tao
Wang, Jinyu
Xie, Kaizhou
Dai, Guojun
MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title_full MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title_fullStr MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title_full_unstemmed MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title_short MicroRNA-7 Targets the KLF4 Gene to Regulate the Proliferation and Differentiation of Chicken Primary Myoblasts
title_sort microrna-7 targets the klf4 gene to regulate the proliferation and differentiation of chicken primary myoblasts
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530283/
https://www.ncbi.nlm.nih.gov/pubmed/33193566
http://dx.doi.org/10.3389/fgene.2020.00842
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