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Expression and splicing mediate distinct biological signals
BACKGROUND: Through alternative splicing, most human genes produce multiple isoforms in a cell-, tissue-, and disease-specific manner. Numerous studies show that alternative splicing is essential for development, diseases, and their treatments. Despite these important examples, the extent and biolog...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588054/ https://www.ncbi.nlm.nih.gov/pubmed/37858135 http://dx.doi.org/10.1186/s12915-023-01724-w |
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author | Dam, Søren Helweg Olsen, Lars Rønn Vitting-Seerup, Kristoffer |
author_facet | Dam, Søren Helweg Olsen, Lars Rønn Vitting-Seerup, Kristoffer |
author_sort | Dam, Søren Helweg |
collection | PubMed |
description | BACKGROUND: Through alternative splicing, most human genes produce multiple isoforms in a cell-, tissue-, and disease-specific manner. Numerous studies show that alternative splicing is essential for development, diseases, and their treatments. Despite these important examples, the extent and biological relevance of splicing are currently unknown. RESULTS: To solve this problem, we developed pairedGSEA and used it to profile transcriptional changes in 100 representative RNA-seq datasets. Our systematic analysis demonstrates that changes in splicing, on average, contribute to 48.1% of the biological signal in expression analyses. Gene-set enrichment analysis furthermore indicates that expression and splicing both convey shared and distinct biological signals. CONCLUSIONS: These findings establish alternative splicing as a major regulator of the human condition and suggest that most contemporary RNA-seq studies likely miss out on critical biological insights. We anticipate our results will contribute to the transition from a gene-centric to an isoform-centric research paradigm. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01724-w. |
format | Online Article Text |
id | pubmed-10588054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105880542023-10-21 Expression and splicing mediate distinct biological signals Dam, Søren Helweg Olsen, Lars Rønn Vitting-Seerup, Kristoffer BMC Biol Research Article BACKGROUND: Through alternative splicing, most human genes produce multiple isoforms in a cell-, tissue-, and disease-specific manner. Numerous studies show that alternative splicing is essential for development, diseases, and their treatments. Despite these important examples, the extent and biological relevance of splicing are currently unknown. RESULTS: To solve this problem, we developed pairedGSEA and used it to profile transcriptional changes in 100 representative RNA-seq datasets. Our systematic analysis demonstrates that changes in splicing, on average, contribute to 48.1% of the biological signal in expression analyses. Gene-set enrichment analysis furthermore indicates that expression and splicing both convey shared and distinct biological signals. CONCLUSIONS: These findings establish alternative splicing as a major regulator of the human condition and suggest that most contemporary RNA-seq studies likely miss out on critical biological insights. We anticipate our results will contribute to the transition from a gene-centric to an isoform-centric research paradigm. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01724-w. BioMed Central 2023-10-20 /pmc/articles/PMC10588054/ /pubmed/37858135 http://dx.doi.org/10.1186/s12915-023-01724-w Text en © The Author(s) 2023 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 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 Dam, Søren Helweg Olsen, Lars Rønn Vitting-Seerup, Kristoffer Expression and splicing mediate distinct biological signals |
title | Expression and splicing mediate distinct biological signals |
title_full | Expression and splicing mediate distinct biological signals |
title_fullStr | Expression and splicing mediate distinct biological signals |
title_full_unstemmed | Expression and splicing mediate distinct biological signals |
title_short | Expression and splicing mediate distinct biological signals |
title_sort | expression and splicing mediate distinct biological signals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588054/ https://www.ncbi.nlm.nih.gov/pubmed/37858135 http://dx.doi.org/10.1186/s12915-023-01724-w |
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