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Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs

BACKGROUND: N(6)-methyladenosine (m(6)A) refers to the methylation modification of N(6) position of RNA adenine, a dynamic reversible RNA epigenetic modification that plays an important regulatory role in a variety of life processes. In this study, we used MeRIP-Seq and RNA-Seq of the longissimus do...

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Autores principales: Dou, Yaqing, Wei, Yilin, Zhang, Zhe, Li, Chenlei, Song, Chenglei, Liu, Yingke, Qi, Kunlong, Li, Xinjian, Li, Xiuling, Qiao, Ruimin, Wang, Kejun, Yang, Feng, Han, Xuelei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161540/
https://www.ncbi.nlm.nih.gov/pubmed/37142996
http://dx.doi.org/10.1186/s12864-023-09346-w
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author Dou, Yaqing
Wei, Yilin
Zhang, Zhe
Li, Chenlei
Song, Chenglei
Liu, Yingke
Qi, Kunlong
Li, Xinjian
Li, Xiuling
Qiao, Ruimin
Wang, Kejun
Yang, Feng
Han, Xuelei
author_facet Dou, Yaqing
Wei, Yilin
Zhang, Zhe
Li, Chenlei
Song, Chenglei
Liu, Yingke
Qi, Kunlong
Li, Xinjian
Li, Xiuling
Qiao, Ruimin
Wang, Kejun
Yang, Feng
Han, Xuelei
author_sort Dou, Yaqing
collection PubMed
description BACKGROUND: N(6)-methyladenosine (m(6)A) refers to the methylation modification of N(6) position of RNA adenine, a dynamic reversible RNA epigenetic modification that plays an important regulatory role in a variety of life processes. In this study, we used MeRIP-Seq and RNA-Seq of the longissimus dorsi (LD) muscle of adult (QA) and newborn (QN) Queshan Black pigs to screen key genes with m(6)A modification involved in muscle growth by bioinformatics analysis. RESULTS: A total of 23,445 and 25,465 m(6)A peaks were found in the whole genomes of QA and QN, respectively. Among them, 613 methylation peaks were significantly different (DMPs) and 579 genes were defined as differentially methylated genes (DMGs). Compared with the QN group, there were 1,874 significantly differentially expressed genes (DEGs) in QA group, including 620 up-regulated and 1,254 down-regulated genes. In order to investigate the relationship between m(6)A and mRNA expression in the muscle of Queshan Black pigs at different periods, a combined analysis of MeRIP-Seq and RNA-Seq showed that 88 genes were significantly different at both levels. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes results showed that DEGs and DMGs were mainly involved in skeletal muscle tissue development, FoxO signaling pathway, MAPK signaling pathway, insulin signaling pathway, PI3K–Akt signaling pathway, and Wnt signaling pathway. Four DEGs (IGF1R, CCND2, MYOD1 and FOS) and four DMGs (CCND2, PHKB, BIN1 and FUT2), which are closely related to skeletal muscle development, were selected as candidate genes for verification, and the results were consistent with the sequencing results, which indicated the reliability of the sequencing results. CONCLUSIONS: These results lay the foundation for understanding the specific regulatory mechanisms of growth in Queshan Black pigs, and provide theoretical references for further research on the role of m(6)A in muscle development and breed optimization selection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09346-w.
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spelling pubmed-101615402023-05-06 Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs Dou, Yaqing Wei, Yilin Zhang, Zhe Li, Chenlei Song, Chenglei Liu, Yingke Qi, Kunlong Li, Xinjian Li, Xiuling Qiao, Ruimin Wang, Kejun Yang, Feng Han, Xuelei BMC Genomics Research BACKGROUND: N(6)-methyladenosine (m(6)A) refers to the methylation modification of N(6) position of RNA adenine, a dynamic reversible RNA epigenetic modification that plays an important regulatory role in a variety of life processes. In this study, we used MeRIP-Seq and RNA-Seq of the longissimus dorsi (LD) muscle of adult (QA) and newborn (QN) Queshan Black pigs to screen key genes with m(6)A modification involved in muscle growth by bioinformatics analysis. RESULTS: A total of 23,445 and 25,465 m(6)A peaks were found in the whole genomes of QA and QN, respectively. Among them, 613 methylation peaks were significantly different (DMPs) and 579 genes were defined as differentially methylated genes (DMGs). Compared with the QN group, there were 1,874 significantly differentially expressed genes (DEGs) in QA group, including 620 up-regulated and 1,254 down-regulated genes. In order to investigate the relationship between m(6)A and mRNA expression in the muscle of Queshan Black pigs at different periods, a combined analysis of MeRIP-Seq and RNA-Seq showed that 88 genes were significantly different at both levels. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes results showed that DEGs and DMGs were mainly involved in skeletal muscle tissue development, FoxO signaling pathway, MAPK signaling pathway, insulin signaling pathway, PI3K–Akt signaling pathway, and Wnt signaling pathway. Four DEGs (IGF1R, CCND2, MYOD1 and FOS) and four DMGs (CCND2, PHKB, BIN1 and FUT2), which are closely related to skeletal muscle development, were selected as candidate genes for verification, and the results were consistent with the sequencing results, which indicated the reliability of the sequencing results. CONCLUSIONS: These results lay the foundation for understanding the specific regulatory mechanisms of growth in Queshan Black pigs, and provide theoretical references for further research on the role of m(6)A in muscle development and breed optimization selection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09346-w. BioMed Central 2023-05-04 /pmc/articles/PMC10161540/ /pubmed/37142996 http://dx.doi.org/10.1186/s12864-023-09346-w Text en © The Author(s) 2023 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
Dou, Yaqing
Wei, Yilin
Zhang, Zhe
Li, Chenlei
Song, Chenglei
Liu, Yingke
Qi, Kunlong
Li, Xinjian
Li, Xiuling
Qiao, Ruimin
Wang, Kejun
Yang, Feng
Han, Xuelei
Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title_full Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title_fullStr Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title_full_unstemmed Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title_short Transcriptome-wide analysis of RNA m(6)A methylation regulation of muscle development in Queshan Black pigs
title_sort transcriptome-wide analysis of rna m(6)a methylation regulation of muscle development in queshan black pigs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161540/
https://www.ncbi.nlm.nih.gov/pubmed/37142996
http://dx.doi.org/10.1186/s12864-023-09346-w
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