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Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes
BACKGROUND: Alternative splicing is a key mechanism underlying cellular differentiation and a driver of complexity in mammalian neuronal tissues. However, understanding of which isoforms are differentially used or expressed and how this affects cellular differentiation remains unclear. Long read seq...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744310/ https://www.ncbi.nlm.nih.gov/pubmed/35012468 http://dx.doi.org/10.1186/s12864-021-08261-2 |
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author | Wright, David J. Hall, Nicola A. L. Irish, Naomi Man, Angela L. Glynn, Will Mould, Arne Angeles, Alejandro De Los Angiolini, Emily Swarbreck, David Gharbi, Karim Tunbridge, Elizabeth M. Haerty, Wilfried |
author_facet | Wright, David J. Hall, Nicola A. L. Irish, Naomi Man, Angela L. Glynn, Will Mould, Arne Angeles, Alejandro De Los Angiolini, Emily Swarbreck, David Gharbi, Karim Tunbridge, Elizabeth M. Haerty, Wilfried |
author_sort | Wright, David J. |
collection | PubMed |
description | BACKGROUND: Alternative splicing is a key mechanism underlying cellular differentiation and a driver of complexity in mammalian neuronal tissues. However, understanding of which isoforms are differentially used or expressed and how this affects cellular differentiation remains unclear. Long read sequencing allows full-length transcript recovery and quantification, enabling transcript-level analysis of alternative splicing processes and how these change with cell state. Here, we utilise Oxford Nanopore Technologies sequencing to produce a custom annotation of a well-studied human neuroblastoma cell line SH-SY5Y, and to characterise isoform expression and usage across differentiation. RESULTS: We identify many previously unannotated features, including a novel transcript of the voltage-gated calcium channel subunit gene, CACNA2D2. We show differential expression and usage of transcripts during differentiation identifying candidates for future research into state change regulation. CONCLUSIONS: Our work highlights the potential of long read sequencing to uncover previously unknown transcript diversity and mechanisms influencing alternative splicing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08261-2. |
format | Online Article Text |
id | pubmed-8744310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87443102022-01-11 Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes Wright, David J. Hall, Nicola A. L. Irish, Naomi Man, Angela L. Glynn, Will Mould, Arne Angeles, Alejandro De Los Angiolini, Emily Swarbreck, David Gharbi, Karim Tunbridge, Elizabeth M. Haerty, Wilfried BMC Genomics Research Article BACKGROUND: Alternative splicing is a key mechanism underlying cellular differentiation and a driver of complexity in mammalian neuronal tissues. However, understanding of which isoforms are differentially used or expressed and how this affects cellular differentiation remains unclear. Long read sequencing allows full-length transcript recovery and quantification, enabling transcript-level analysis of alternative splicing processes and how these change with cell state. Here, we utilise Oxford Nanopore Technologies sequencing to produce a custom annotation of a well-studied human neuroblastoma cell line SH-SY5Y, and to characterise isoform expression and usage across differentiation. RESULTS: We identify many previously unannotated features, including a novel transcript of the voltage-gated calcium channel subunit gene, CACNA2D2. We show differential expression and usage of transcripts during differentiation identifying candidates for future research into state change regulation. CONCLUSIONS: Our work highlights the potential of long read sequencing to uncover previously unknown transcript diversity and mechanisms influencing alternative splicing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08261-2. BioMed Central 2022-01-10 /pmc/articles/PMC8744310/ /pubmed/35012468 http://dx.doi.org/10.1186/s12864-021-08261-2 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Wright, David J. Hall, Nicola A. L. Irish, Naomi Man, Angela L. Glynn, Will Mould, Arne Angeles, Alejandro De Los Angiolini, Emily Swarbreck, David Gharbi, Karim Tunbridge, Elizabeth M. Haerty, Wilfried Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title | Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title_full | Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title_fullStr | Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title_full_unstemmed | Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title_short | Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
title_sort | long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744310/ https://www.ncbi.nlm.nih.gov/pubmed/35012468 http://dx.doi.org/10.1186/s12864-021-08261-2 |
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