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Nuclear pore components affect distinct stages of intron-containing gene expression
Several nuclear pore-associated factors, including the SUMO-protease Ulp1, have been proposed to prevent the export of intron-containing messenger ribonucleoparticles (mRNPs) in yeast. However, the molecular mechanisms of this nuclear pore-dependent mRNA quality control, including the sumoylated tar...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417180/ https://www.ncbi.nlm.nih.gov/pubmed/25845599 http://dx.doi.org/10.1093/nar/gkv280 |
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author | Bonnet, Amandine Bretes, Hugo Palancade, Benoit |
author_facet | Bonnet, Amandine Bretes, Hugo Palancade, Benoit |
author_sort | Bonnet, Amandine |
collection | PubMed |
description | Several nuclear pore-associated factors, including the SUMO-protease Ulp1, have been proposed to prevent the export of intron-containing messenger ribonucleoparticles (mRNPs) in yeast. However, the molecular mechanisms of this nuclear pore-dependent mRNA quality control, including the sumoylated targets of Ulp1, have remained unidentified. Here, we demonstrate that the apparent ‘pre-mRNA leakage’ phenotype arising upon ULP1 inactivation is shared by sumoylation mutants of the THO complex, an early mRNP biogenesis factor. Importantly, we establish that alteration of THO complex activity differentially impairs the expression of intronless and intron-containing reporter genes, rather than triggering bona fide ‘pre-mRNA leakage’. Indeed, we show that the presence of introns within THO target genes attenuates the effect of THO inactivation on their transcription. Epistasis analyses further clarify that different nuclear pore components influence intron-containing gene expression at distinct stages. Ulp1, whose maintenance at nuclear pores depends on the Nup84 complex, impacts on THO-dependent gene expression, whereas the nuclear basket-associated Mlp1/Pml39 proteins prevent pre-mRNA export at a later stage, contributing to mRNA quality control. Our study thus highlights the multiplicity of mechanisms by which nuclear pores contribute to gene expression, and further provides the first evidence that intronic sequences can alleviate early mRNP biogenesis defects. |
format | Online Article Text |
id | pubmed-4417180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44171802015-05-12 Nuclear pore components affect distinct stages of intron-containing gene expression Bonnet, Amandine Bretes, Hugo Palancade, Benoit Nucleic Acids Res RNA Several nuclear pore-associated factors, including the SUMO-protease Ulp1, have been proposed to prevent the export of intron-containing messenger ribonucleoparticles (mRNPs) in yeast. However, the molecular mechanisms of this nuclear pore-dependent mRNA quality control, including the sumoylated targets of Ulp1, have remained unidentified. Here, we demonstrate that the apparent ‘pre-mRNA leakage’ phenotype arising upon ULP1 inactivation is shared by sumoylation mutants of the THO complex, an early mRNP biogenesis factor. Importantly, we establish that alteration of THO complex activity differentially impairs the expression of intronless and intron-containing reporter genes, rather than triggering bona fide ‘pre-mRNA leakage’. Indeed, we show that the presence of introns within THO target genes attenuates the effect of THO inactivation on their transcription. Epistasis analyses further clarify that different nuclear pore components influence intron-containing gene expression at distinct stages. Ulp1, whose maintenance at nuclear pores depends on the Nup84 complex, impacts on THO-dependent gene expression, whereas the nuclear basket-associated Mlp1/Pml39 proteins prevent pre-mRNA export at a later stage, contributing to mRNA quality control. Our study thus highlights the multiplicity of mechanisms by which nuclear pores contribute to gene expression, and further provides the first evidence that intronic sequences can alleviate early mRNP biogenesis defects. Oxford University Press 2015-04-30 2015-04-06 /pmc/articles/PMC4417180/ /pubmed/25845599 http://dx.doi.org/10.1093/nar/gkv280 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA Bonnet, Amandine Bretes, Hugo Palancade, Benoit Nuclear pore components affect distinct stages of intron-containing gene expression |
title | Nuclear pore components affect distinct stages of intron-containing gene expression |
title_full | Nuclear pore components affect distinct stages of intron-containing gene expression |
title_fullStr | Nuclear pore components affect distinct stages of intron-containing gene expression |
title_full_unstemmed | Nuclear pore components affect distinct stages of intron-containing gene expression |
title_short | Nuclear pore components affect distinct stages of intron-containing gene expression |
title_sort | nuclear pore components affect distinct stages of intron-containing gene expression |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417180/ https://www.ncbi.nlm.nih.gov/pubmed/25845599 http://dx.doi.org/10.1093/nar/gkv280 |
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