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Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing

Piglet diarrhea is a swine disease responsible for serious economic impacts in the pig industry. Clostridium perfringens beta2 toxin (CPB2), which is a major toxin of C. perfringens type C, may cause intestinal diseases in many domestic animals. N(6)-methyladenosine (m(6)A) RNA methylation plays cri...

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Autores principales: Zhang, Juanli, Yang, Qiaoli, Yang, Jiaojiao, Gao, Xiaoli, Luo, Ruirui, Huang, Xiaoyu, Yan, Zunqiang, Wang, Pengfei, Wang, Wei, Xie, Kaihui, Zhang, Bo, Gun, Shuangbao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560698/
https://www.ncbi.nlm.nih.gov/pubmed/34737761
http://dx.doi.org/10.3389/fgene.2021.689748
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author Zhang, Juanli
Yang, Qiaoli
Yang, Jiaojiao
Gao, Xiaoli
Luo, Ruirui
Huang, Xiaoyu
Yan, Zunqiang
Wang, Pengfei
Wang, Wei
Xie, Kaihui
Zhang, Bo
Gun, Shuangbao
author_facet Zhang, Juanli
Yang, Qiaoli
Yang, Jiaojiao
Gao, Xiaoli
Luo, Ruirui
Huang, Xiaoyu
Yan, Zunqiang
Wang, Pengfei
Wang, Wei
Xie, Kaihui
Zhang, Bo
Gun, Shuangbao
author_sort Zhang, Juanli
collection PubMed
description Piglet diarrhea is a swine disease responsible for serious economic impacts in the pig industry. Clostridium perfringens beta2 toxin (CPB2), which is a major toxin of C. perfringens type C, may cause intestinal diseases in many domestic animals. N(6)-methyladenosine (m(6)A) RNA methylation plays critical roles in many immune and inflammatory diseases in livestock and other animals. However, the role of m(6)A methylation in porcine intestinal epithelial (IPEC-J2) cells exposed to CPB2 has not been studied. To address this issue, we treated IPEC-J2 cells with CPB2 toxin and then quantified methylation-related enzyme expression by RT-qPCR and assessed the m(6)A methylation status of the samples by colorimetric N(6)-methyladenosine quantification. The results showed that the methylation enzymes changed to varying degrees while the m(6)A methylation level increased (p < 0.01). On this basis, we performed N(6)-methyladenosine sequencing (m(6)A-seq) and RNA sequencing (RNA-seq) to examine the detailed m(6)A modifications and gene expression of the IPEC-J2 cells following CPB2 toxin exposure. Our results indicated that 1,448 m(6)A modification sites, including 437 up-regulated and 1,011 down-regulated, differed significantly between CPB2 toxin exposed cells and non-exposed cells (p < 0.05). KEGG pathway analysis results showed that m(6)A peaks up-regulated genes (n = 394) were mainly enriched in cancer, Cushing syndrome and Wnt signaling pathways, while m(6)A peaks down-regulated genes (n = 920) were mainly associated with apoptosis, small cell lung cancer, and the herpes simplex virus 1 infection signaling pathway. Furthermore, gene expression (RNA-seq data) analysis identified 1,636 differentially expressed genes (DEGs), of which 1,094 were up-regulated and 542 were down-regulated in the toxin exposed group compared with the control group. In addition, the down-regulated genes were involved in the Hippo and Wnt signaling pathways. Interestingly, the combined results of m(6)A-seq and RNA-seq identified genes with up-regulated m(6)A peaks but with down-regulated expression, here referred to as “hyper-down” genes (n = 18), which were mainly enriched in the Wnt signaling pathway. Therefore, we speculate that the genes in the Wnt signaling pathway may be modified by m(6)A methylation in CPB2-induced IPEC-J2 cells. These findings provide new insights enabling further exploration of the mechanisms underlying piglet diarrhea caused by CPB2 toxin.
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spelling pubmed-85606982021-11-03 Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing Zhang, Juanli Yang, Qiaoli Yang, Jiaojiao Gao, Xiaoli Luo, Ruirui Huang, Xiaoyu Yan, Zunqiang Wang, Pengfei Wang, Wei Xie, Kaihui Zhang, Bo Gun, Shuangbao Front Genet Genetics Piglet diarrhea is a swine disease responsible for serious economic impacts in the pig industry. Clostridium perfringens beta2 toxin (CPB2), which is a major toxin of C. perfringens type C, may cause intestinal diseases in many domestic animals. N(6)-methyladenosine (m(6)A) RNA methylation plays critical roles in many immune and inflammatory diseases in livestock and other animals. However, the role of m(6)A methylation in porcine intestinal epithelial (IPEC-J2) cells exposed to CPB2 has not been studied. To address this issue, we treated IPEC-J2 cells with CPB2 toxin and then quantified methylation-related enzyme expression by RT-qPCR and assessed the m(6)A methylation status of the samples by colorimetric N(6)-methyladenosine quantification. The results showed that the methylation enzymes changed to varying degrees while the m(6)A methylation level increased (p < 0.01). On this basis, we performed N(6)-methyladenosine sequencing (m(6)A-seq) and RNA sequencing (RNA-seq) to examine the detailed m(6)A modifications and gene expression of the IPEC-J2 cells following CPB2 toxin exposure. Our results indicated that 1,448 m(6)A modification sites, including 437 up-regulated and 1,011 down-regulated, differed significantly between CPB2 toxin exposed cells and non-exposed cells (p < 0.05). KEGG pathway analysis results showed that m(6)A peaks up-regulated genes (n = 394) were mainly enriched in cancer, Cushing syndrome and Wnt signaling pathways, while m(6)A peaks down-regulated genes (n = 920) were mainly associated with apoptosis, small cell lung cancer, and the herpes simplex virus 1 infection signaling pathway. Furthermore, gene expression (RNA-seq data) analysis identified 1,636 differentially expressed genes (DEGs), of which 1,094 were up-regulated and 542 were down-regulated in the toxin exposed group compared with the control group. In addition, the down-regulated genes were involved in the Hippo and Wnt signaling pathways. Interestingly, the combined results of m(6)A-seq and RNA-seq identified genes with up-regulated m(6)A peaks but with down-regulated expression, here referred to as “hyper-down” genes (n = 18), which were mainly enriched in the Wnt signaling pathway. Therefore, we speculate that the genes in the Wnt signaling pathway may be modified by m(6)A methylation in CPB2-induced IPEC-J2 cells. These findings provide new insights enabling further exploration of the mechanisms underlying piglet diarrhea caused by CPB2 toxin. Frontiers Media S.A. 2021-10-19 /pmc/articles/PMC8560698/ /pubmed/34737761 http://dx.doi.org/10.3389/fgene.2021.689748 Text en Copyright © 2021 Zhang, Yang, Yang, Gao, Luo, Huang, Yan, Wang, Wang, Xie, Zhang and Gun. https://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 Genetics
Zhang, Juanli
Yang, Qiaoli
Yang, Jiaojiao
Gao, Xiaoli
Luo, Ruirui
Huang, Xiaoyu
Yan, Zunqiang
Wang, Pengfei
Wang, Wei
Xie, Kaihui
Zhang, Bo
Gun, Shuangbao
Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title_full Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title_fullStr Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title_full_unstemmed Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title_short Comprehensive Analysis of Transcriptome-wide m(6)A Methylome Upon Clostridium perfringens Beta2 Toxin Exposure in Porcine Intestinal Epithelial Cells by m(6)A Sequencing
title_sort comprehensive analysis of transcriptome-wide m(6)a methylome upon clostridium perfringens beta2 toxin exposure in porcine intestinal epithelial cells by m(6)a sequencing
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560698/
https://www.ncbi.nlm.nih.gov/pubmed/34737761
http://dx.doi.org/10.3389/fgene.2021.689748
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