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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...

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Autores principales: Dam, Søren Helweg, Olsen, Lars Rønn, Vitting-Seerup, Kristoffer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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.
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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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