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Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing

Previous studies have demonstrated the highly specific expression of circular RNAs (circRNAs) in different tissues and organisms, but the cellular architecture of circRNA has never been fully characterized. Here, we present a collection of 171 full-length single-cell RNA-seq datasets to explore the...

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Autores principales: Wu, Wanying, Zhang, Jinyang, Cao, Xiaofei, Cai, Zhengyi, Zhao, Fangqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187688/
https://www.ncbi.nlm.nih.gov/pubmed/35688820
http://dx.doi.org/10.1038/s41467-022-30963-8
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author Wu, Wanying
Zhang, Jinyang
Cao, Xiaofei
Cai, Zhengyi
Zhao, Fangqing
author_facet Wu, Wanying
Zhang, Jinyang
Cao, Xiaofei
Cai, Zhengyi
Zhao, Fangqing
author_sort Wu, Wanying
collection PubMed
description Previous studies have demonstrated the highly specific expression of circular RNAs (circRNAs) in different tissues and organisms, but the cellular architecture of circRNA has never been fully characterized. Here, we present a collection of 171 full-length single-cell RNA-seq datasets to explore the cellular landscape of circRNAs in human and mouse tissues. Through large-scale integrative analysis, we identify a total of 139,643 human and 214,747 mouse circRNAs in these scRNA-seq libraries. We validate the detected circRNAs with the integration of 11 bulk RNA-seq based resources, where 216,602 high-confidence circRNAs are uniquely detected in the single-cell cohort. We reveal the cell-type-specific expression pattern of circRNAs in brain samples, developing embryos, and breast tumors. We identify the uniquely expressed circRNAs in different cell types and validate their performance in tumor-infiltrating immune cell composition deconvolution. This study expands our knowledge of circRNA expression to the single-cell level and provides a useful resource for exploring circRNAs at this unprecedented resolution.
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spelling pubmed-91876882022-06-12 Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing Wu, Wanying Zhang, Jinyang Cao, Xiaofei Cai, Zhengyi Zhao, Fangqing Nat Commun Article Previous studies have demonstrated the highly specific expression of circular RNAs (circRNAs) in different tissues and organisms, but the cellular architecture of circRNA has never been fully characterized. Here, we present a collection of 171 full-length single-cell RNA-seq datasets to explore the cellular landscape of circRNAs in human and mouse tissues. Through large-scale integrative analysis, we identify a total of 139,643 human and 214,747 mouse circRNAs in these scRNA-seq libraries. We validate the detected circRNAs with the integration of 11 bulk RNA-seq based resources, where 216,602 high-confidence circRNAs are uniquely detected in the single-cell cohort. We reveal the cell-type-specific expression pattern of circRNAs in brain samples, developing embryos, and breast tumors. We identify the uniquely expressed circRNAs in different cell types and validate their performance in tumor-infiltrating immune cell composition deconvolution. This study expands our knowledge of circRNA expression to the single-cell level and provides a useful resource for exploring circRNAs at this unprecedented resolution. Nature Publishing Group UK 2022-06-10 /pmc/articles/PMC9187688/ /pubmed/35688820 http://dx.doi.org/10.1038/s41467-022-30963-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wu, Wanying
Zhang, Jinyang
Cao, Xiaofei
Cai, Zhengyi
Zhao, Fangqing
Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title_full Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title_fullStr Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title_full_unstemmed Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title_short Exploring the cellular landscape of circular RNAs using full-length single-cell RNA sequencing
title_sort exploring the cellular landscape of circular rnas using full-length single-cell rna sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187688/
https://www.ncbi.nlm.nih.gov/pubmed/35688820
http://dx.doi.org/10.1038/s41467-022-30963-8
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