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MiR-34c represses muscle development by forming a regulatory loop with Notch1

Since pork accounts for about 40% of global meat consumption, the pig is an important economic animal for meat production. Pig is also a useful medical model for humans due to its similarity in size and physiology. Understanding the mechanism of muscle development has great implication for animal br...

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Autores principales: Hou, Lianjie, Xu, Jian, Li, Huaqin, Ou, Jinxin, Jiao, Yiren, Hu, Chingyuan, Wang, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571228/
https://www.ncbi.nlm.nih.gov/pubmed/28839212
http://dx.doi.org/10.1038/s41598-017-09688-y
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author Hou, Lianjie
Xu, Jian
Li, Huaqin
Ou, Jinxin
Jiao, Yiren
Hu, Chingyuan
Wang, Chong
author_facet Hou, Lianjie
Xu, Jian
Li, Huaqin
Ou, Jinxin
Jiao, Yiren
Hu, Chingyuan
Wang, Chong
author_sort Hou, Lianjie
collection PubMed
description Since pork accounts for about 40% of global meat consumption, the pig is an important economic animal for meat production. Pig is also a useful medical model for humans due to its similarity in size and physiology. Understanding the mechanism of muscle development has great implication for animal breeding and human health. Previous studies showed porcine muscle satellite cells (PSCs) are important for postnatal skeletal muscle growth, and Notch1 signaling pathway and miRNAs regulate the skeletal muscle development. Notch1 signal pathway regulates the transcription of certain types of miRNAs which further affects target gene expression. However, the specific relationship between Notch1 and miRNAs during muscle development has not been established. We found miR-34c is decreased in PSCs overexpressed N1ICD. Through the overexpression and inhibition of mi-34c, we demonstrated that miR-34c inhibits PSCs proliferation and promotes PSCs differentiation. Using dual-luciferase reporter assay and Chromatin immunoprecipitation, we demonstrate there is a reciprocal regulatory loop between Notch1 and miR-34c. Furthermore, injection of miR-34c lentivirus into mice caused repression of gastrocnemius muscle development. In summary, our data revealed that miR-34c can form a regulatory loop with Notch1 to repress muscle development, and this result expands our understanding of muscle development mechanism.
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spelling pubmed-55712282017-09-01 MiR-34c represses muscle development by forming a regulatory loop with Notch1 Hou, Lianjie Xu, Jian Li, Huaqin Ou, Jinxin Jiao, Yiren Hu, Chingyuan Wang, Chong Sci Rep Article Since pork accounts for about 40% of global meat consumption, the pig is an important economic animal for meat production. Pig is also a useful medical model for humans due to its similarity in size and physiology. Understanding the mechanism of muscle development has great implication for animal breeding and human health. Previous studies showed porcine muscle satellite cells (PSCs) are important for postnatal skeletal muscle growth, and Notch1 signaling pathway and miRNAs regulate the skeletal muscle development. Notch1 signal pathway regulates the transcription of certain types of miRNAs which further affects target gene expression. However, the specific relationship between Notch1 and miRNAs during muscle development has not been established. We found miR-34c is decreased in PSCs overexpressed N1ICD. Through the overexpression and inhibition of mi-34c, we demonstrated that miR-34c inhibits PSCs proliferation and promotes PSCs differentiation. Using dual-luciferase reporter assay and Chromatin immunoprecipitation, we demonstrate there is a reciprocal regulatory loop between Notch1 and miR-34c. Furthermore, injection of miR-34c lentivirus into mice caused repression of gastrocnemius muscle development. In summary, our data revealed that miR-34c can form a regulatory loop with Notch1 to repress muscle development, and this result expands our understanding of muscle development mechanism. Nature Publishing Group UK 2017-08-24 /pmc/articles/PMC5571228/ /pubmed/28839212 http://dx.doi.org/10.1038/s41598-017-09688-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hou, Lianjie
Xu, Jian
Li, Huaqin
Ou, Jinxin
Jiao, Yiren
Hu, Chingyuan
Wang, Chong
MiR-34c represses muscle development by forming a regulatory loop with Notch1
title MiR-34c represses muscle development by forming a regulatory loop with Notch1
title_full MiR-34c represses muscle development by forming a regulatory loop with Notch1
title_fullStr MiR-34c represses muscle development by forming a regulatory loop with Notch1
title_full_unstemmed MiR-34c represses muscle development by forming a regulatory loop with Notch1
title_short MiR-34c represses muscle development by forming a regulatory loop with Notch1
title_sort mir-34c represses muscle development by forming a regulatory loop with notch1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571228/
https://www.ncbi.nlm.nih.gov/pubmed/28839212
http://dx.doi.org/10.1038/s41598-017-09688-y
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