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The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins
The highly conserved 5’–3’ exonuclease Xrn1 regulates gene expression in eukaryotes by coupling nuclear DNA transcription to cytosolic mRNA decay. By integrating transcriptome-wide analyses of translation with biochemical and functional studies, we demonstrate an unanticipated regulatory role of Xrn...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428865/ https://www.ncbi.nlm.nih.gov/pubmed/30899024 http://dx.doi.org/10.1038/s41467-019-09199-6 |
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author | Blasco-Moreno, Bernat de Campos-Mata, Leire Böttcher, René García-Martínez, José Jungfleisch, Jennifer Nedialkova, Danny D. Chattopadhyay, Shiladitya Gas, María-Eugenia Oliva, Baldomero Pérez-Ortín, José E. Leidel, Sebastian A. Choder, Mordechai Díez, Juana |
author_facet | Blasco-Moreno, Bernat de Campos-Mata, Leire Böttcher, René García-Martínez, José Jungfleisch, Jennifer Nedialkova, Danny D. Chattopadhyay, Shiladitya Gas, María-Eugenia Oliva, Baldomero Pérez-Ortín, José E. Leidel, Sebastian A. Choder, Mordechai Díez, Juana |
author_sort | Blasco-Moreno, Bernat |
collection | PubMed |
description | The highly conserved 5’–3’ exonuclease Xrn1 regulates gene expression in eukaryotes by coupling nuclear DNA transcription to cytosolic mRNA decay. By integrating transcriptome-wide analyses of translation with biochemical and functional studies, we demonstrate an unanticipated regulatory role of Xrn1 in protein synthesis. Xrn1 promotes translation of a specific group of transcripts encoding membrane proteins. Xrn1-dependence for translation is linked to poor structural RNA contexts for translation initiation, is mediated by interactions with components of the translation initiation machinery and correlates with an Xrn1-dependence for mRNA localization at the endoplasmic reticulum, the translation compartment of membrane proteins. Importantly, for this group of mRNAs, Xrn1 stimulates transcription, mRNA translation and decay. Our results uncover a crosstalk between the three major stages of gene expression coordinated by Xrn1 to maintain appropriate levels of membrane proteins. |
format | Online Article Text |
id | pubmed-6428865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64288652019-03-25 The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins Blasco-Moreno, Bernat de Campos-Mata, Leire Böttcher, René García-Martínez, José Jungfleisch, Jennifer Nedialkova, Danny D. Chattopadhyay, Shiladitya Gas, María-Eugenia Oliva, Baldomero Pérez-Ortín, José E. Leidel, Sebastian A. Choder, Mordechai Díez, Juana Nat Commun Article The highly conserved 5’–3’ exonuclease Xrn1 regulates gene expression in eukaryotes by coupling nuclear DNA transcription to cytosolic mRNA decay. By integrating transcriptome-wide analyses of translation with biochemical and functional studies, we demonstrate an unanticipated regulatory role of Xrn1 in protein synthesis. Xrn1 promotes translation of a specific group of transcripts encoding membrane proteins. Xrn1-dependence for translation is linked to poor structural RNA contexts for translation initiation, is mediated by interactions with components of the translation initiation machinery and correlates with an Xrn1-dependence for mRNA localization at the endoplasmic reticulum, the translation compartment of membrane proteins. Importantly, for this group of mRNAs, Xrn1 stimulates transcription, mRNA translation and decay. Our results uncover a crosstalk between the three major stages of gene expression coordinated by Xrn1 to maintain appropriate levels of membrane proteins. Nature Publishing Group UK 2019-03-21 /pmc/articles/PMC6428865/ /pubmed/30899024 http://dx.doi.org/10.1038/s41467-019-09199-6 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Blasco-Moreno, Bernat de Campos-Mata, Leire Böttcher, René García-Martínez, José Jungfleisch, Jennifer Nedialkova, Danny D. Chattopadhyay, Shiladitya Gas, María-Eugenia Oliva, Baldomero Pérez-Ortín, José E. Leidel, Sebastian A. Choder, Mordechai Díez, Juana The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title | The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title_full | The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title_fullStr | The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title_full_unstemmed | The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title_short | The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins |
title_sort | exonuclease xrn1 activates transcription and translation of mrnas encoding membrane proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428865/ https://www.ncbi.nlm.nih.gov/pubmed/30899024 http://dx.doi.org/10.1038/s41467-019-09199-6 |
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