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Comprehensive identification of alternative back-splicing in human tissue transcriptomes

Circular RNAs (circRNAs) are covalently closed RNAs derived from back-splicing of genes across eukaryotes. Through alternative back-splicing (ABS), a single gene produces multiple circRNAs sharing the same back-splice site. Although many ABS events have recently been discovered, to what extent ABS i...

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Autores principales: Zhang, Peng, Zhang, Xiao-Ou, Jiang, Tingting, Cai, Lingling, Huang, Xiao, Liu, Qi, Li, Dan, Lu, Aiping, Liu, Yan, Xue, Wen, Weng, Zhiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038940/
https://www.ncbi.nlm.nih.gov/pubmed/31974555
http://dx.doi.org/10.1093/nar/gkaa005
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author Zhang, Peng
Zhang, Xiao-Ou
Jiang, Tingting
Cai, Lingling
Huang, Xiao
Liu, Qi
Li, Dan
Lu, Aiping
Liu, Yan
Xue, Wen
Zhang, Peng
Weng, Zhiping
author_facet Zhang, Peng
Zhang, Xiao-Ou
Jiang, Tingting
Cai, Lingling
Huang, Xiao
Liu, Qi
Li, Dan
Lu, Aiping
Liu, Yan
Xue, Wen
Zhang, Peng
Weng, Zhiping
author_sort Zhang, Peng
collection PubMed
description Circular RNAs (circRNAs) are covalently closed RNAs derived from back-splicing of genes across eukaryotes. Through alternative back-splicing (ABS), a single gene produces multiple circRNAs sharing the same back-splice site. Although many ABS events have recently been discovered, to what extent ABS involves in circRNA biogenesis and how it is regulated in different human tissues still remain elusive. Here, we reported an in-depth analysis of ABS events in 90 human tissue transcriptomes. We observed that ABS occurred for about 84% circRNAs. Interestingly, alternative 5′ back-splicing occurs more prevalently than alternative 3′ back-splicing, and both of them are tissue-specific, especially enriched in brain tissues. In addition, the patterns of ABS events in different brain regions are similar to each other and are more complex than the patterns in non-brain tissues. Finally, the intron length and abundance of Alu elements positively correlated with ABS event complexity, and the predominant circRNAs had longer flanking introns and more Alu elements than other circRNAs in the same ABS event. Together, our results represent a resource for circRNA research—we expanded the repertoire of ABS events of circRNAs in human tissue transcriptomes and provided insights into the complexity of circRNA biogenesis, expression, and regulation.
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spelling pubmed-70389402020-03-02 Comprehensive identification of alternative back-splicing in human tissue transcriptomes Zhang, Peng Zhang, Xiao-Ou Jiang, Tingting Cai, Lingling Huang, Xiao Liu, Qi Li, Dan Lu, Aiping Liu, Yan Xue, Wen Zhang, Peng Weng, Zhiping Nucleic Acids Res Data Resources and Analyses Circular RNAs (circRNAs) are covalently closed RNAs derived from back-splicing of genes across eukaryotes. Through alternative back-splicing (ABS), a single gene produces multiple circRNAs sharing the same back-splice site. Although many ABS events have recently been discovered, to what extent ABS involves in circRNA biogenesis and how it is regulated in different human tissues still remain elusive. Here, we reported an in-depth analysis of ABS events in 90 human tissue transcriptomes. We observed that ABS occurred for about 84% circRNAs. Interestingly, alternative 5′ back-splicing occurs more prevalently than alternative 3′ back-splicing, and both of them are tissue-specific, especially enriched in brain tissues. In addition, the patterns of ABS events in different brain regions are similar to each other and are more complex than the patterns in non-brain tissues. Finally, the intron length and abundance of Alu elements positively correlated with ABS event complexity, and the predominant circRNAs had longer flanking introns and more Alu elements than other circRNAs in the same ABS event. Together, our results represent a resource for circRNA research—we expanded the repertoire of ABS events of circRNAs in human tissue transcriptomes and provided insights into the complexity of circRNA biogenesis, expression, and regulation. Oxford University Press 2020-02-28 2020-01-24 /pmc/articles/PMC7038940/ /pubmed/31974555 http://dx.doi.org/10.1093/nar/gkaa005 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Data Resources and Analyses
Zhang, Peng
Zhang, Xiao-Ou
Jiang, Tingting
Cai, Lingling
Huang, Xiao
Liu, Qi
Li, Dan
Lu, Aiping
Liu, Yan
Xue, Wen
Zhang, Peng
Weng, Zhiping
Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title_full Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title_fullStr Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title_full_unstemmed Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title_short Comprehensive identification of alternative back-splicing in human tissue transcriptomes
title_sort comprehensive identification of alternative back-splicing in human tissue transcriptomes
topic Data Resources and Analyses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038940/
https://www.ncbi.nlm.nih.gov/pubmed/31974555
http://dx.doi.org/10.1093/nar/gkaa005
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