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Identification of crucial circRNAs in skeletal muscle during chicken embryonic development

BACKGROUND: Chicken provides humans with a large amount of animal protein every year, in which skeletal muscle plays a leading role. The embryonic skeletal muscle development determines the number of muscle fibers and will affect the muscle production of chickens. CircRNAs are involved in a variety...

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Autores principales: Wu, Pengfei, Zhou, Kaizhi, Zhang, Jin, Ling, Xuanze, Zhang, Xinchao, Zhang, Li, Li, Peifeng, Wei, Qingyu, Zhang, Tao, Wang, Xinglong, Zhang, Genxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052468/
https://www.ncbi.nlm.nih.gov/pubmed/35484498
http://dx.doi.org/10.1186/s12864-022-08588-4
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author Wu, Pengfei
Zhou, Kaizhi
Zhang, Jin
Ling, Xuanze
Zhang, Xinchao
Zhang, Li
Li, Peifeng
Wei, Qingyu
Zhang, Tao
Wang, Xinglong
Zhang, Genxi
author_facet Wu, Pengfei
Zhou, Kaizhi
Zhang, Jin
Ling, Xuanze
Zhang, Xinchao
Zhang, Li
Li, Peifeng
Wei, Qingyu
Zhang, Tao
Wang, Xinglong
Zhang, Genxi
author_sort Wu, Pengfei
collection PubMed
description BACKGROUND: Chicken provides humans with a large amount of animal protein every year, in which skeletal muscle plays a leading role. The embryonic skeletal muscle development determines the number of muscle fibers and will affect the muscle production of chickens. CircRNAs are involved in a variety of important biological processes, including muscle development. However, studies on circRNAs in the chicken embryo muscle development are still lacking. RESULTS: In the study, we collected chicken leg muscles at 14 and 20-day embryo ages both in the fast- and slow-growing groups for RNA-seq. We identified 245 and 440 differentially expressed (DE) circRNAs in the comparison group F14vsF20 and S14vsS20 respectively. GO enrichment analysis for the host genes of DE circRNAs showed that biological process (BP) terms in the top 20 related to growth in F14vsF20 were found such as positive regulation of transcription involved in G1/S phase of mitotic cell cycle, multicellular organismal macromolecule metabolic process, and multicellular organismal metabolic process. In group S14vsS20, we also found some BP terms associated with growth in the top 20 including actomyosin structure organization, actin cytoskeleton organization and myofibril assembly. A total of 7 significantly enriched pathways were obtained, containing Adherens junction and Tight junction. Further analysis of those pathways found three crucial host genes MYH9, YBX3, IGF1R in both fast- and slow-growing groups, three important host genes CTNNA3, AFDN and CREBBP only in the fast-growing group, and six host genes FGFR2, ACTN2, COL1A2, CDC42, DOCK1 and MYL3 only in the slow-growing group. In addition, circRNA-miRNA network also revealed some key regulation pairs such as novel_circ_0007646-miR-1625-5p, novel_circ_0007646-miR-1680-5p, novel_circ_0008913-miR-148b-5p, novel_circ_0008906-miR-148b-5p and novel_circ_0001640-miR-1759-3p. CONCLUSIONS: Comprehensive analysis of circRNAs and their targets would contribute to a better understanding of the molecular mechanisms in poultry skeletal muscle and it also plays an important guiding role in the next research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08588-4.
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spelling pubmed-90524682022-04-30 Identification of crucial circRNAs in skeletal muscle during chicken embryonic development Wu, Pengfei Zhou, Kaizhi Zhang, Jin Ling, Xuanze Zhang, Xinchao Zhang, Li Li, Peifeng Wei, Qingyu Zhang, Tao Wang, Xinglong Zhang, Genxi BMC Genomics Research BACKGROUND: Chicken provides humans with a large amount of animal protein every year, in which skeletal muscle plays a leading role. The embryonic skeletal muscle development determines the number of muscle fibers and will affect the muscle production of chickens. CircRNAs are involved in a variety of important biological processes, including muscle development. However, studies on circRNAs in the chicken embryo muscle development are still lacking. RESULTS: In the study, we collected chicken leg muscles at 14 and 20-day embryo ages both in the fast- and slow-growing groups for RNA-seq. We identified 245 and 440 differentially expressed (DE) circRNAs in the comparison group F14vsF20 and S14vsS20 respectively. GO enrichment analysis for the host genes of DE circRNAs showed that biological process (BP) terms in the top 20 related to growth in F14vsF20 were found such as positive regulation of transcription involved in G1/S phase of mitotic cell cycle, multicellular organismal macromolecule metabolic process, and multicellular organismal metabolic process. In group S14vsS20, we also found some BP terms associated with growth in the top 20 including actomyosin structure organization, actin cytoskeleton organization and myofibril assembly. A total of 7 significantly enriched pathways were obtained, containing Adherens junction and Tight junction. Further analysis of those pathways found three crucial host genes MYH9, YBX3, IGF1R in both fast- and slow-growing groups, three important host genes CTNNA3, AFDN and CREBBP only in the fast-growing group, and six host genes FGFR2, ACTN2, COL1A2, CDC42, DOCK1 and MYL3 only in the slow-growing group. In addition, circRNA-miRNA network also revealed some key regulation pairs such as novel_circ_0007646-miR-1625-5p, novel_circ_0007646-miR-1680-5p, novel_circ_0008913-miR-148b-5p, novel_circ_0008906-miR-148b-5p and novel_circ_0001640-miR-1759-3p. CONCLUSIONS: Comprehensive analysis of circRNAs and their targets would contribute to a better understanding of the molecular mechanisms in poultry skeletal muscle and it also plays an important guiding role in the next research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08588-4. BioMed Central 2022-04-28 /pmc/articles/PMC9052468/ /pubmed/35484498 http://dx.doi.org/10.1186/s12864-022-08588-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wu, Pengfei
Zhou, Kaizhi
Zhang, Jin
Ling, Xuanze
Zhang, Xinchao
Zhang, Li
Li, Peifeng
Wei, Qingyu
Zhang, Tao
Wang, Xinglong
Zhang, Genxi
Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title_full Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title_fullStr Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title_full_unstemmed Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title_short Identification of crucial circRNAs in skeletal muscle during chicken embryonic development
title_sort identification of crucial circrnas in skeletal muscle during chicken embryonic development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052468/
https://www.ncbi.nlm.nih.gov/pubmed/35484498
http://dx.doi.org/10.1186/s12864-022-08588-4
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