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Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development

Many circular RNAs (circRNAs) have been discovered in various tissues and cell types in pig. However, the temporal expression pattern of circRNAs during porcine embryonic muscle development remains unclear. Here, we present a panorama view of circRNA expression in embryonic muscle development at 33-...

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Autores principales: Hong, Linjun, Gu, Ting, He, Yanjuan, Zhou, Chen, Hu, Qun, Wang, Xingwang, Zheng, Enqin, Huang, Sixiu, Xu, Zheng, Yang, Jie, Yang, Huaqiang, Li, Zicong, Liu, Dewu, Cai, Gengyuan, Wu, Zhenfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877547/
https://www.ncbi.nlm.nih.gov/pubmed/31803743
http://dx.doi.org/10.3389/fcell.2019.00289
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author Hong, Linjun
Gu, Ting
He, Yanjuan
Zhou, Chen
Hu, Qun
Wang, Xingwang
Zheng, Enqin
Huang, Sixiu
Xu, Zheng
Yang, Jie
Yang, Huaqiang
Li, Zicong
Liu, Dewu
Cai, Gengyuan
Wu, Zhenfang
author_facet Hong, Linjun
Gu, Ting
He, Yanjuan
Zhou, Chen
Hu, Qun
Wang, Xingwang
Zheng, Enqin
Huang, Sixiu
Xu, Zheng
Yang, Jie
Yang, Huaqiang
Li, Zicong
Liu, Dewu
Cai, Gengyuan
Wu, Zhenfang
author_sort Hong, Linjun
collection PubMed
description Many circular RNAs (circRNAs) have been discovered in various tissues and cell types in pig. However, the temporal expression pattern of circRNAs during porcine embryonic muscle development remains unclear. Here, we present a panorama view of circRNA expression in embryonic muscle development at 33-, 65-, and 90-days post-coitus (dpc) from Duroc pigs. An unbiased analysis reveals that more than 5,000 circRNAs specifically express in embryonic muscle development. The amount and complexity of circRNA expression is most pronounced in skeletal muscle at day 33 of gestation. Our circRNAs annotation analyses show that “hot-spot” genes produce multiple circRNA isoforms and RNA binding protein (RBPs) may regulate the biogenesis of circRNAs. Furthermore, we observed that host genes of differentially expressed circRNA across porcine muscle development are enriched in skeletal muscle function. A competing endogenous RNA (ceRNA) network analysis of circRNAs reveals that circRNAs regulate muscle gene expression by functioning as miRNA sponges. Finally, our experimental validation demonstrated that circTUT7 regulate the expression of HMG20B in a ceRNA mechanism. Our analyses show that circRNAs are dynamically expressed and interacting with muscle genes through ceRNA manner, suggesting their critical functions in embryonic skeletal muscle development.
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spelling pubmed-68775472019-12-04 Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development Hong, Linjun Gu, Ting He, Yanjuan Zhou, Chen Hu, Qun Wang, Xingwang Zheng, Enqin Huang, Sixiu Xu, Zheng Yang, Jie Yang, Huaqiang Li, Zicong Liu, Dewu Cai, Gengyuan Wu, Zhenfang Front Cell Dev Biol Cell and Developmental Biology Many circular RNAs (circRNAs) have been discovered in various tissues and cell types in pig. However, the temporal expression pattern of circRNAs during porcine embryonic muscle development remains unclear. Here, we present a panorama view of circRNA expression in embryonic muscle development at 33-, 65-, and 90-days post-coitus (dpc) from Duroc pigs. An unbiased analysis reveals that more than 5,000 circRNAs specifically express in embryonic muscle development. The amount and complexity of circRNA expression is most pronounced in skeletal muscle at day 33 of gestation. Our circRNAs annotation analyses show that “hot-spot” genes produce multiple circRNA isoforms and RNA binding protein (RBPs) may regulate the biogenesis of circRNAs. Furthermore, we observed that host genes of differentially expressed circRNA across porcine muscle development are enriched in skeletal muscle function. A competing endogenous RNA (ceRNA) network analysis of circRNAs reveals that circRNAs regulate muscle gene expression by functioning as miRNA sponges. Finally, our experimental validation demonstrated that circTUT7 regulate the expression of HMG20B in a ceRNA mechanism. Our analyses show that circRNAs are dynamically expressed and interacting with muscle genes through ceRNA manner, suggesting their critical functions in embryonic skeletal muscle development. Frontiers Media S.A. 2019-11-19 /pmc/articles/PMC6877547/ /pubmed/31803743 http://dx.doi.org/10.3389/fcell.2019.00289 Text en Copyright © 2019 Hong, Gu, He, Zhou, Hu, Wang, Zheng, Huang, Xu, Yang, Yang, Li, Liu, Cai and Wu. 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 Cell and Developmental Biology
Hong, Linjun
Gu, Ting
He, Yanjuan
Zhou, Chen
Hu, Qun
Wang, Xingwang
Zheng, Enqin
Huang, Sixiu
Xu, Zheng
Yang, Jie
Yang, Huaqiang
Li, Zicong
Liu, Dewu
Cai, Gengyuan
Wu, Zhenfang
Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title_full Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title_fullStr Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title_full_unstemmed Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title_short Genome-Wide Analysis of Circular RNAs Mediated ceRNA Regulation in Porcine Embryonic Muscle Development
title_sort genome-wide analysis of circular rnas mediated cerna regulation in porcine embryonic muscle development
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877547/
https://www.ncbi.nlm.nih.gov/pubmed/31803743
http://dx.doi.org/10.3389/fcell.2019.00289
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