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isoCirc catalogs full-length circular RNA isoforms in human transcriptomes

Circular RNAs (circRNAs) have emerged as an important class of functional RNA molecules. Short-read RNA sequencing (RNA-seq) is a widely used strategy to identify circRNAs. However, an inherent limitation of short-read RNA-seq is that it does not experimentally determine the full-length sequences an...

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Autores principales: Xin, Ruijiao, Gao, Yan, Gao, Yuan, Wang, Robert, Kadash-Edmondson, Kathryn E., Liu, Bo, Wang, Yadong, Lin, Lan, Xing, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803736/
https://www.ncbi.nlm.nih.gov/pubmed/33436621
http://dx.doi.org/10.1038/s41467-020-20459-8
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author Xin, Ruijiao
Gao, Yan
Gao, Yuan
Wang, Robert
Kadash-Edmondson, Kathryn E.
Liu, Bo
Wang, Yadong
Lin, Lan
Xing, Yi
author_facet Xin, Ruijiao
Gao, Yan
Gao, Yuan
Wang, Robert
Kadash-Edmondson, Kathryn E.
Liu, Bo
Wang, Yadong
Lin, Lan
Xing, Yi
author_sort Xin, Ruijiao
collection PubMed
description Circular RNAs (circRNAs) have emerged as an important class of functional RNA molecules. Short-read RNA sequencing (RNA-seq) is a widely used strategy to identify circRNAs. However, an inherent limitation of short-read RNA-seq is that it does not experimentally determine the full-length sequences and exact exonic compositions of circRNAs. Here, we report isoCirc, a strategy for sequencing full-length circRNA isoforms, using rolling circle amplification followed by nanopore long-read sequencing. We describe an integrated computational pipeline to reliably characterize full-length circRNA isoforms using isoCirc data. Using isoCirc, we generate a comprehensive catalog of 107,147 full-length circRNA isoforms across 12 human tissues and one human cell line (HEK293), including 40,628 isoforms ≥500 nt in length. We identify widespread alternative splicing events within the internal part of circRNAs, including 720 retained intron events corresponding to a class of exon-intron circRNAs (EIciRNAs). Collectively, isoCirc and the companion dataset provide a useful strategy and resource for studying circRNAs in human transcriptomes.
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spelling pubmed-78037362021-01-21 isoCirc catalogs full-length circular RNA isoforms in human transcriptomes Xin, Ruijiao Gao, Yan Gao, Yuan Wang, Robert Kadash-Edmondson, Kathryn E. Liu, Bo Wang, Yadong Lin, Lan Xing, Yi Nat Commun Article Circular RNAs (circRNAs) have emerged as an important class of functional RNA molecules. Short-read RNA sequencing (RNA-seq) is a widely used strategy to identify circRNAs. However, an inherent limitation of short-read RNA-seq is that it does not experimentally determine the full-length sequences and exact exonic compositions of circRNAs. Here, we report isoCirc, a strategy for sequencing full-length circRNA isoforms, using rolling circle amplification followed by nanopore long-read sequencing. We describe an integrated computational pipeline to reliably characterize full-length circRNA isoforms using isoCirc data. Using isoCirc, we generate a comprehensive catalog of 107,147 full-length circRNA isoforms across 12 human tissues and one human cell line (HEK293), including 40,628 isoforms ≥500 nt in length. We identify widespread alternative splicing events within the internal part of circRNAs, including 720 retained intron events corresponding to a class of exon-intron circRNAs (EIciRNAs). Collectively, isoCirc and the companion dataset provide a useful strategy and resource for studying circRNAs in human transcriptomes. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7803736/ /pubmed/33436621 http://dx.doi.org/10.1038/s41467-020-20459-8 Text en © The Author(s) 2021 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xin, Ruijiao
Gao, Yan
Gao, Yuan
Wang, Robert
Kadash-Edmondson, Kathryn E.
Liu, Bo
Wang, Yadong
Lin, Lan
Xing, Yi
isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title_full isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title_fullStr isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title_full_unstemmed isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title_short isoCirc catalogs full-length circular RNA isoforms in human transcriptomes
title_sort isocirc catalogs full-length circular rna isoforms in human transcriptomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803736/
https://www.ncbi.nlm.nih.gov/pubmed/33436621
http://dx.doi.org/10.1038/s41467-020-20459-8
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