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Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae
There is increasing evidence from yeast to humans that pre-mRNA splicing occurs mainly cotranscriptionally, such that splicing and transcription are functionally coupled. Currently, there is little insight into the contribution of the core transcription elongation machinery to cotranscriptional spli...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800482/ https://www.ncbi.nlm.nih.gov/pubmed/31289129 http://dx.doi.org/10.1261/rna.070425.119 |
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author | Maudlin, Isabella E. Beggs, Jean D. |
author_facet | Maudlin, Isabella E. Beggs, Jean D. |
author_sort | Maudlin, Isabella E. |
collection | PubMed |
description | There is increasing evidence from yeast to humans that pre-mRNA splicing occurs mainly cotranscriptionally, such that splicing and transcription are functionally coupled. Currently, there is little insight into the contribution of the core transcription elongation machinery to cotranscriptional spliceosome assembly and pre-mRNA splicing. Spt5 is a member of the core transcription elongation machinery and an essential protein, whose absence in budding yeast causes defects in pre-mRNA splicing. To determine how Spt5 affects pre-mRNA splicing, we used the auxin-inducible degron system to conditionally deplete Spt5 in Saccharomyces cerevisiae and assayed effects on cotranscriptional spliceosome assembly and splicing. We show that Spt5 is needed for efficient splicing and for the accumulation of U5 snRNPs at intron-containing genes, and therefore for stable cotranscriptional assembly of spliceosomes. The defect in cotranscriptional spliceosome assembly can explain the relatively mild splicing defect as being a consequence of the failure of cotranscriptional splicing. Coimmunoprecipitation of Spt5 with core spliceosomal proteins and all spliceosomal snRNAs suggests a model whereby Spt5 promotes cotranscriptional pre-mRNA splicing by stabilizing the association of U5 snRNP with spliceosome complexes as they assemble on the nascent transcript. If this phenomenon is conserved in higher eukaryotes, it has the potential to be important for cotranscriptional regulation of alternative splicing. |
format | Online Article Text |
id | pubmed-6800482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68004822019-10-31 Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae Maudlin, Isabella E. Beggs, Jean D. RNA Article There is increasing evidence from yeast to humans that pre-mRNA splicing occurs mainly cotranscriptionally, such that splicing and transcription are functionally coupled. Currently, there is little insight into the contribution of the core transcription elongation machinery to cotranscriptional spliceosome assembly and pre-mRNA splicing. Spt5 is a member of the core transcription elongation machinery and an essential protein, whose absence in budding yeast causes defects in pre-mRNA splicing. To determine how Spt5 affects pre-mRNA splicing, we used the auxin-inducible degron system to conditionally deplete Spt5 in Saccharomyces cerevisiae and assayed effects on cotranscriptional spliceosome assembly and splicing. We show that Spt5 is needed for efficient splicing and for the accumulation of U5 snRNPs at intron-containing genes, and therefore for stable cotranscriptional assembly of spliceosomes. The defect in cotranscriptional spliceosome assembly can explain the relatively mild splicing defect as being a consequence of the failure of cotranscriptional splicing. Coimmunoprecipitation of Spt5 with core spliceosomal proteins and all spliceosomal snRNAs suggests a model whereby Spt5 promotes cotranscriptional pre-mRNA splicing by stabilizing the association of U5 snRNP with spliceosome complexes as they assemble on the nascent transcript. If this phenomenon is conserved in higher eukaryotes, it has the potential to be important for cotranscriptional regulation of alternative splicing. Cold Spring Harbor Laboratory Press 2019-10 /pmc/articles/PMC6800482/ /pubmed/31289129 http://dx.doi.org/10.1261/rna.070425.119 Text en © 2019 Maudlin and Beggs; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Maudlin, Isabella E. Beggs, Jean D. Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title_full | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title_fullStr | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title_full_unstemmed | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title_short | Spt5 modulates cotranscriptional spliceosome assembly in Saccharomyces cerevisiae |
title_sort | spt5 modulates cotranscriptional spliceosome assembly in saccharomyces cerevisiae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800482/ https://www.ncbi.nlm.nih.gov/pubmed/31289129 http://dx.doi.org/10.1261/rna.070425.119 |
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