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CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken

Circular RNAs (circRNAs) play a significant regulatory role during skeletal muscle development. To identify circRNAs during postnatal skeletal muscle development in chickens, we constructed 12 cDNA libraries from breast muscle tissues of Chinese Gushi chickens at 6, 14, 22, and 30 weeks and performe...

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Autores principales: Yuan, Pengtao, Zhao, Yinli, Li, Hongtai, Li, Shuaihao, Fan, Shengxin, Zhai, Bin, Li, Yuanfang, Han, Ruili, Liu, Xiaojun, Tian, Yadong, Kang, Xiangtao, Zhang, Yanhua, Li, Guoxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689937/
https://www.ncbi.nlm.nih.gov/pubmed/36360215
http://dx.doi.org/10.3390/genes13111974
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author Yuan, Pengtao
Zhao, Yinli
Li, Hongtai
Li, Shuaihao
Fan, Shengxin
Zhai, Bin
Li, Yuanfang
Han, Ruili
Liu, Xiaojun
Tian, Yadong
Kang, Xiangtao
Zhang, Yanhua
Li, Guoxi
author_facet Yuan, Pengtao
Zhao, Yinli
Li, Hongtai
Li, Shuaihao
Fan, Shengxin
Zhai, Bin
Li, Yuanfang
Han, Ruili
Liu, Xiaojun
Tian, Yadong
Kang, Xiangtao
Zhang, Yanhua
Li, Guoxi
author_sort Yuan, Pengtao
collection PubMed
description Circular RNAs (circRNAs) play a significant regulatory role during skeletal muscle development. To identify circRNAs during postnatal skeletal muscle development in chickens, we constructed 12 cDNA libraries from breast muscle tissues of Chinese Gushi chickens at 6, 14, 22, and 30 weeks and performed RNA sequencing. In total, 2112 circRNAs were identified, and among them 79.92% were derived from exons. CircRNAs are distributed on all chromosomes of chickens, especially chromosomes 1–9 and Z. Bioinformatics analysis showed that each circRNA had an average of 38 miRNA binding sites, 61.32% of which have internal ribosomal entry site (IRES) elements. Furthermore, in total 543 differentially expressed circRNAs (DE-circRNAs) were identified. Functional enrichment analysis revealed that DE-circRNAs source genes are engaged in biological processes and muscle development-related pathways; for example, cell differentiation, sarcomere, and myofibril formation, mTOR signaling pathway, and TGF-β signaling pathway, etc. We also established a competitive endogenous RNA (ceRNA) regulatory network associated with skeletal muscle development. The results in this report indicate that circRNAs can mediate the development of chicken skeletal muscle by means of a complex ceRNA network among circRNAs, miRNAs, genes, and pathways. The findings of this study might help increase the number of known circRNAs in skeletal muscle tissue and offer a worthwhile resource to further investigate the function of circRNAs in chicken skeletal muscle development.
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spelling pubmed-96899372022-11-25 CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken Yuan, Pengtao Zhao, Yinli Li, Hongtai Li, Shuaihao Fan, Shengxin Zhai, Bin Li, Yuanfang Han, Ruili Liu, Xiaojun Tian, Yadong Kang, Xiangtao Zhang, Yanhua Li, Guoxi Genes (Basel) Article Circular RNAs (circRNAs) play a significant regulatory role during skeletal muscle development. To identify circRNAs during postnatal skeletal muscle development in chickens, we constructed 12 cDNA libraries from breast muscle tissues of Chinese Gushi chickens at 6, 14, 22, and 30 weeks and performed RNA sequencing. In total, 2112 circRNAs were identified, and among them 79.92% were derived from exons. CircRNAs are distributed on all chromosomes of chickens, especially chromosomes 1–9 and Z. Bioinformatics analysis showed that each circRNA had an average of 38 miRNA binding sites, 61.32% of which have internal ribosomal entry site (IRES) elements. Furthermore, in total 543 differentially expressed circRNAs (DE-circRNAs) were identified. Functional enrichment analysis revealed that DE-circRNAs source genes are engaged in biological processes and muscle development-related pathways; for example, cell differentiation, sarcomere, and myofibril formation, mTOR signaling pathway, and TGF-β signaling pathway, etc. We also established a competitive endogenous RNA (ceRNA) regulatory network associated with skeletal muscle development. The results in this report indicate that circRNAs can mediate the development of chicken skeletal muscle by means of a complex ceRNA network among circRNAs, miRNAs, genes, and pathways. The findings of this study might help increase the number of known circRNAs in skeletal muscle tissue and offer a worthwhile resource to further investigate the function of circRNAs in chicken skeletal muscle development. MDPI 2022-10-29 /pmc/articles/PMC9689937/ /pubmed/36360215 http://dx.doi.org/10.3390/genes13111974 Text en © 2022 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
Yuan, Pengtao
Zhao, Yinli
Li, Hongtai
Li, Shuaihao
Fan, Shengxin
Zhai, Bin
Li, Yuanfang
Han, Ruili
Liu, Xiaojun
Tian, Yadong
Kang, Xiangtao
Zhang, Yanhua
Li, Guoxi
CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title_full CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title_fullStr CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title_full_unstemmed CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title_short CircRNAs Related to Breast Muscle Development and Their Interaction Regulatory Network in Gushi Chicken
title_sort circrnas related to breast muscle development and their interaction regulatory network in gushi chicken
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689937/
https://www.ncbi.nlm.nih.gov/pubmed/36360215
http://dx.doi.org/10.3390/genes13111974
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