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Trend analysis of the role of circular RNA in goat skeletal muscle development

BACKGROUND: Circular RNA (circRNA) is produced during the splicing of mRNA (in addition to linear splicing) and is part of the gene regulatory network. The temporal expression patterns the different developmental stages were inseparable from these molecules’ function. RESULTS: Skeletal muscles of An...

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Autores principales: Ling, Yinghui, Zheng, Qi, Zhu, Lu, Xu, Lina, Sui, Menghua, Zhang, Yunhai, Liu, Ya, Fang, Fugui, Chu, Mingxing, Ma, Yuehui, Zhang, Xiaorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063781/
https://www.ncbi.nlm.nih.gov/pubmed/32151242
http://dx.doi.org/10.1186/s12864-020-6649-2
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author Ling, Yinghui
Zheng, Qi
Zhu, Lu
Xu, Lina
Sui, Menghua
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Chu, Mingxing
Ma, Yuehui
Zhang, Xiaorong
author_facet Ling, Yinghui
Zheng, Qi
Zhu, Lu
Xu, Lina
Sui, Menghua
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Chu, Mingxing
Ma, Yuehui
Zhang, Xiaorong
author_sort Ling, Yinghui
collection PubMed
description BACKGROUND: Circular RNA (circRNA) is produced during the splicing of mRNA (in addition to linear splicing) and is part of the gene regulatory network. The temporal expression patterns the different developmental stages were inseparable from these molecules’ function. RESULTS: Skeletal muscles of Anhui white goat (AWG) across seven fetal to postnatal development stages were sequenced and 21 RNA sequencing libraries were constructed. We thereby identified 9090 circRNAs and analyzed their molecular properties, temporal expression patterns, and potential functions at the different stages. CircRNAs showed complexities and diversity of formation as the same host gene produces multiple isoforms of these nucleic acids with different expression profiles. The differential expression of 2881 circRNAs (DECs, P < 0.05) was identified and four were randomly selected and validated by qPCR. Moreover, 1118 DECs under strict selected (SDECs, |log2(FC)| > 2 and P-adj value < 0.01) showed 4 expression trends (Clusters 0, 19, 16 and 18). Cluster 0 molecules had increasing expression at all stages with effects on muscle through metabolism, regulation of enzyme activity, and biosynthesis. Cluster 16 circRNAs had high expression in the early and late stages and are involved in “Wnt signaling pathway”, “AMPK signaling pathway” and others. Cluster 18 molecules were mainly expressed at F120 and participate in “cytoskeletal protein binding”, “Notch signaling pathway” and so on. Cluster 19 circRNAs were down-regulated at all stages and related to muscle structure and development. Lastly, the SDECs divided the period of skeletal muscle development into three transitional stages: stage 1 (F45 to F90), which related to muscle satellite cell proliferation and muscle fiber structure; stage 2 (F90 to B1), in which the attachment of the cytoplasmic surface to the actin cytoskeleton initiates; and stage 3, which involved the “cGMP-PKG signaling pathway”. Moreover, the paraffin sections messages also validated that there are three transitional stages of skeletal muscle development. CONCLUSION: Our current study provides a catalog of goat muscle-related circRNAs that can stratify skeletal muscle development fetus 45 days to newborn 90 days into three developmental stages. These findings better our understanding of functional transitions during mammalian muscle development.
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spelling pubmed-70637812020-03-13 Trend analysis of the role of circular RNA in goat skeletal muscle development Ling, Yinghui Zheng, Qi Zhu, Lu Xu, Lina Sui, Menghua Zhang, Yunhai Liu, Ya Fang, Fugui Chu, Mingxing Ma, Yuehui Zhang, Xiaorong BMC Genomics Research Article BACKGROUND: Circular RNA (circRNA) is produced during the splicing of mRNA (in addition to linear splicing) and is part of the gene regulatory network. The temporal expression patterns the different developmental stages were inseparable from these molecules’ function. RESULTS: Skeletal muscles of Anhui white goat (AWG) across seven fetal to postnatal development stages were sequenced and 21 RNA sequencing libraries were constructed. We thereby identified 9090 circRNAs and analyzed their molecular properties, temporal expression patterns, and potential functions at the different stages. CircRNAs showed complexities and diversity of formation as the same host gene produces multiple isoforms of these nucleic acids with different expression profiles. The differential expression of 2881 circRNAs (DECs, P < 0.05) was identified and four were randomly selected and validated by qPCR. Moreover, 1118 DECs under strict selected (SDECs, |log2(FC)| > 2 and P-adj value < 0.01) showed 4 expression trends (Clusters 0, 19, 16 and 18). Cluster 0 molecules had increasing expression at all stages with effects on muscle through metabolism, regulation of enzyme activity, and biosynthesis. Cluster 16 circRNAs had high expression in the early and late stages and are involved in “Wnt signaling pathway”, “AMPK signaling pathway” and others. Cluster 18 molecules were mainly expressed at F120 and participate in “cytoskeletal protein binding”, “Notch signaling pathway” and so on. Cluster 19 circRNAs were down-regulated at all stages and related to muscle structure and development. Lastly, the SDECs divided the period of skeletal muscle development into three transitional stages: stage 1 (F45 to F90), which related to muscle satellite cell proliferation and muscle fiber structure; stage 2 (F90 to B1), in which the attachment of the cytoplasmic surface to the actin cytoskeleton initiates; and stage 3, which involved the “cGMP-PKG signaling pathway”. Moreover, the paraffin sections messages also validated that there are three transitional stages of skeletal muscle development. CONCLUSION: Our current study provides a catalog of goat muscle-related circRNAs that can stratify skeletal muscle development fetus 45 days to newborn 90 days into three developmental stages. These findings better our understanding of functional transitions during mammalian muscle development. BioMed Central 2020-03-10 /pmc/articles/PMC7063781/ /pubmed/32151242 http://dx.doi.org/10.1186/s12864-020-6649-2 Text en © The Author(s). 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Ling, Yinghui
Zheng, Qi
Zhu, Lu
Xu, Lina
Sui, Menghua
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Chu, Mingxing
Ma, Yuehui
Zhang, Xiaorong
Trend analysis of the role of circular RNA in goat skeletal muscle development
title Trend analysis of the role of circular RNA in goat skeletal muscle development
title_full Trend analysis of the role of circular RNA in goat skeletal muscle development
title_fullStr Trend analysis of the role of circular RNA in goat skeletal muscle development
title_full_unstemmed Trend analysis of the role of circular RNA in goat skeletal muscle development
title_short Trend analysis of the role of circular RNA in goat skeletal muscle development
title_sort trend analysis of the role of circular rna in goat skeletal muscle development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063781/
https://www.ncbi.nlm.nih.gov/pubmed/32151242
http://dx.doi.org/10.1186/s12864-020-6649-2
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