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Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
Saccharomyces cerevisiae has been used as a model system to investigate the mechanisms of pre-mRNA splicing but only a few examples of alternative splice site usage have been described in this organism. Using RNA-Seq analysis of nonsense-mediated mRNA decay (NMD) mutant strains, we show that many S....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983031/ https://www.ncbi.nlm.nih.gov/pubmed/24722551 http://dx.doi.org/10.1371/journal.pgen.1004249 |
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author | Kawashima, Tadashi Douglass, Stephen Gabunilas, Jason Pellegrini, Matteo Chanfreau, Guillaume F. |
author_facet | Kawashima, Tadashi Douglass, Stephen Gabunilas, Jason Pellegrini, Matteo Chanfreau, Guillaume F. |
author_sort | Kawashima, Tadashi |
collection | PubMed |
description | Saccharomyces cerevisiae has been used as a model system to investigate the mechanisms of pre-mRNA splicing but only a few examples of alternative splice site usage have been described in this organism. Using RNA-Seq analysis of nonsense-mediated mRNA decay (NMD) mutant strains, we show that many S. cerevisiae intron-containing genes exhibit usage of alternative splice sites, but many transcripts generated by splicing at these sites are non-functional because they introduce premature termination codons, leading to degradation by NMD. Analysis of splicing mutants combined with NMD inactivation revealed the role of specific splicing factors in governing the use of these alternative splice sites and identified novel functions for Prp17p in enhancing the use of branchpoint-proximal upstream 3′ splice sites and for Prp18p in suppressing the usage of a non-canonical AUG 3′-splice site in GCR1. The use of non-productive alternative splice sites can be increased in stress conditions in a promoter-dependent manner, contributing to the down-regulation of genes during stress. These results show that alternative splicing is frequent in S. cerevisiae but masked by RNA degradation and that the use of alternative splice sites in this organism is mostly aimed at controlling transcript levels rather than increasing proteome diversity. |
format | Online Article Text |
id | pubmed-3983031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39830312014-04-15 Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae Kawashima, Tadashi Douglass, Stephen Gabunilas, Jason Pellegrini, Matteo Chanfreau, Guillaume F. PLoS Genet Research Article Saccharomyces cerevisiae has been used as a model system to investigate the mechanisms of pre-mRNA splicing but only a few examples of alternative splice site usage have been described in this organism. Using RNA-Seq analysis of nonsense-mediated mRNA decay (NMD) mutant strains, we show that many S. cerevisiae intron-containing genes exhibit usage of alternative splice sites, but many transcripts generated by splicing at these sites are non-functional because they introduce premature termination codons, leading to degradation by NMD. Analysis of splicing mutants combined with NMD inactivation revealed the role of specific splicing factors in governing the use of these alternative splice sites and identified novel functions for Prp17p in enhancing the use of branchpoint-proximal upstream 3′ splice sites and for Prp18p in suppressing the usage of a non-canonical AUG 3′-splice site in GCR1. The use of non-productive alternative splice sites can be increased in stress conditions in a promoter-dependent manner, contributing to the down-regulation of genes during stress. These results show that alternative splicing is frequent in S. cerevisiae but masked by RNA degradation and that the use of alternative splice sites in this organism is mostly aimed at controlling transcript levels rather than increasing proteome diversity. Public Library of Science 2014-04-10 /pmc/articles/PMC3983031/ /pubmed/24722551 http://dx.doi.org/10.1371/journal.pgen.1004249 Text en © 2014 Kawashima et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kawashima, Tadashi Douglass, Stephen Gabunilas, Jason Pellegrini, Matteo Chanfreau, Guillaume F. Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae |
title | Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
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title_full | Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
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title_fullStr | Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
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title_full_unstemmed | Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
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title_short | Widespread Use of Non-productive Alternative Splice Sites in Saccharomyces cerevisiae
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title_sort | widespread use of non-productive alternative splice sites in saccharomyces cerevisiae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983031/ https://www.ncbi.nlm.nih.gov/pubmed/24722551 http://dx.doi.org/10.1371/journal.pgen.1004249 |
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