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Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing

BACKGROUND: RNA editing is a co/posttranscriptional modification mechanism that increases the diversity of transcripts, with potential functional consequences. The advent of next-generation sequencing technologies has enabled the identification of RNA edits at unprecedented throughput and resolution...

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Autores principales: Zhang, Yuebo, Zhang, Longchao, Yue, Jingwei, Wei, Xia, Wang, Ligang, Liu, Xin, Gao, Hongmei, Hou, Xinhua, Zhao, Fuping, Yan, Hua, Wang, Lixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415349/
https://www.ncbi.nlm.nih.gov/pubmed/30911384
http://dx.doi.org/10.1186/s40104-019-0326-9
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author Zhang, Yuebo
Zhang, Longchao
Yue, Jingwei
Wei, Xia
Wang, Ligang
Liu, Xin
Gao, Hongmei
Hou, Xinhua
Zhao, Fuping
Yan, Hua
Wang, Lixian
author_facet Zhang, Yuebo
Zhang, Longchao
Yue, Jingwei
Wei, Xia
Wang, Ligang
Liu, Xin
Gao, Hongmei
Hou, Xinhua
Zhao, Fuping
Yan, Hua
Wang, Lixian
author_sort Zhang, Yuebo
collection PubMed
description BACKGROUND: RNA editing is a co/posttranscriptional modification mechanism that increases the diversity of transcripts, with potential functional consequences. The advent of next-generation sequencing technologies has enabled the identification of RNA edits at unprecedented throughput and resolution. However, our knowledge of RNA editing in swine is still limited. RESULTS: Here, we utilized RES-Scanner to identify RNA editing sites in the brain, subcutaneous fat, heart, liver, muscle, lung and ovary in three 180-day-old Large White gilts based on matched strand-specific RNA sequencing and whole-genome resequencing datasets. In total, we identified 74863 editing sites, and 92.1% of these sites caused adenosine-to-guanosine (A-to-G) conversion. Most A-to-G sites were located in noncoding regions and generally had low editing levels. In total, 151 A-to-G sites were detected in coding regions (CDS), including 94 sites that could lead to nonsynonymous amino acid changes. We provide further evidence supporting a previous observation that pig transcriptomes are highly editable at PRE-1 elements. The number of A-to-G editing sites ranged from 4155 (muscle) to 25001 (brain) across the seven tissues. The expression levels of the ADAR enzymes could explain some but not all of this variation across tissues. The functional analysis of the genes with tissue-specific editing sites in each tissue revealed that RNA editing might play important roles in tissue function. Specifically, more pathways showed significant enrichment in the fat and liver than in other tissues, while no pathway was enriched in the muscle. CONCLUSIONS: This study identified a total of 74863 nonredundant RNA editing sites in seven tissues and revealed the potential importance of RNA editing in tissue function. Our findings largely extend the porcine editome and enhance our understanding of RNA editing in swine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0326-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-64153492019-03-25 Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing Zhang, Yuebo Zhang, Longchao Yue, Jingwei Wei, Xia Wang, Ligang Liu, Xin Gao, Hongmei Hou, Xinhua Zhao, Fuping Yan, Hua Wang, Lixian J Anim Sci Biotechnol Research BACKGROUND: RNA editing is a co/posttranscriptional modification mechanism that increases the diversity of transcripts, with potential functional consequences. The advent of next-generation sequencing technologies has enabled the identification of RNA edits at unprecedented throughput and resolution. However, our knowledge of RNA editing in swine is still limited. RESULTS: Here, we utilized RES-Scanner to identify RNA editing sites in the brain, subcutaneous fat, heart, liver, muscle, lung and ovary in three 180-day-old Large White gilts based on matched strand-specific RNA sequencing and whole-genome resequencing datasets. In total, we identified 74863 editing sites, and 92.1% of these sites caused adenosine-to-guanosine (A-to-G) conversion. Most A-to-G sites were located in noncoding regions and generally had low editing levels. In total, 151 A-to-G sites were detected in coding regions (CDS), including 94 sites that could lead to nonsynonymous amino acid changes. We provide further evidence supporting a previous observation that pig transcriptomes are highly editable at PRE-1 elements. The number of A-to-G editing sites ranged from 4155 (muscle) to 25001 (brain) across the seven tissues. The expression levels of the ADAR enzymes could explain some but not all of this variation across tissues. The functional analysis of the genes with tissue-specific editing sites in each tissue revealed that RNA editing might play important roles in tissue function. Specifically, more pathways showed significant enrichment in the fat and liver than in other tissues, while no pathway was enriched in the muscle. CONCLUSIONS: This study identified a total of 74863 nonredundant RNA editing sites in seven tissues and revealed the potential importance of RNA editing in tissue function. Our findings largely extend the porcine editome and enhance our understanding of RNA editing in swine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0326-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-13 /pmc/articles/PMC6415349/ /pubmed/30911384 http://dx.doi.org/10.1186/s40104-019-0326-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Zhang, Yuebo
Zhang, Longchao
Yue, Jingwei
Wei, Xia
Wang, Ligang
Liu, Xin
Gao, Hongmei
Hou, Xinhua
Zhao, Fuping
Yan, Hua
Wang, Lixian
Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title_full Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title_fullStr Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title_full_unstemmed Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title_short Genome-wide identification of RNA editing in seven porcine tissues by matched DNA and RNA high-throughput sequencing
title_sort genome-wide identification of rna editing in seven porcine tissues by matched dna and rna high-throughput sequencing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415349/
https://www.ncbi.nlm.nih.gov/pubmed/30911384
http://dx.doi.org/10.1186/s40104-019-0326-9
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