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Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress
RNA-binding proteins play a key role in shaping gene expression profiles during stress, however, little is known about the dynamic nature of these interactions and how this influences the kinetics of gene expression. To address this, we developed kinetic cross-linking and analysis of cDNAs (χCRAC),...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432031/ https://www.ncbi.nlm.nih.gov/pubmed/28400552 http://dx.doi.org/10.1038/s41467-017-00025-5 |
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author | van Nues, Rob Schweikert, Gabriele de Leau, Erica Selega, Alina Langford, Andrew Franklin, Ryan Iosub, Ira Wadsworth, Peter Sanguinetti, Guido Granneman, Sander |
author_facet | van Nues, Rob Schweikert, Gabriele de Leau, Erica Selega, Alina Langford, Andrew Franklin, Ryan Iosub, Ira Wadsworth, Peter Sanguinetti, Guido Granneman, Sander |
author_sort | van Nues, Rob |
collection | PubMed |
description | RNA-binding proteins play a key role in shaping gene expression profiles during stress, however, little is known about the dynamic nature of these interactions and how this influences the kinetics of gene expression. To address this, we developed kinetic cross-linking and analysis of cDNAs (χCRAC), an ultraviolet cross-linking method that enabled us to quantitatively measure the dynamics of protein–RNA interactions in vivo on a minute time-scale. Here, using χCRAC we measure the global RNA-binding dynamics of the yeast transcription termination factor Nab3 in response to glucose starvation. These measurements reveal rapid changes in protein–RNA interactions within 1 min following stress imposition. Changes in Nab3 binding are largely independent of alterations in transcription rate during the early stages of stress response, indicating orthogonal transcriptional control mechanisms. We also uncover a function for Nab3 in dampening expression of stress-responsive genes. χCRAC has the potential to greatly enhance our understanding of in vivo dynamics of protein–RNA interactions. |
format | Online Article Text |
id | pubmed-5432031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54320312017-05-18 Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress van Nues, Rob Schweikert, Gabriele de Leau, Erica Selega, Alina Langford, Andrew Franklin, Ryan Iosub, Ira Wadsworth, Peter Sanguinetti, Guido Granneman, Sander Nat Commun Article RNA-binding proteins play a key role in shaping gene expression profiles during stress, however, little is known about the dynamic nature of these interactions and how this influences the kinetics of gene expression. To address this, we developed kinetic cross-linking and analysis of cDNAs (χCRAC), an ultraviolet cross-linking method that enabled us to quantitatively measure the dynamics of protein–RNA interactions in vivo on a minute time-scale. Here, using χCRAC we measure the global RNA-binding dynamics of the yeast transcription termination factor Nab3 in response to glucose starvation. These measurements reveal rapid changes in protein–RNA interactions within 1 min following stress imposition. Changes in Nab3 binding are largely independent of alterations in transcription rate during the early stages of stress response, indicating orthogonal transcriptional control mechanisms. We also uncover a function for Nab3 in dampening expression of stress-responsive genes. χCRAC has the potential to greatly enhance our understanding of in vivo dynamics of protein–RNA interactions. Nature Publishing Group UK 2017-04-11 /pmc/articles/PMC5432031/ /pubmed/28400552 http://dx.doi.org/10.1038/s41467-017-00025-5 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article van Nues, Rob Schweikert, Gabriele de Leau, Erica Selega, Alina Langford, Andrew Franklin, Ryan Iosub, Ira Wadsworth, Peter Sanguinetti, Guido Granneman, Sander Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title | Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title_full | Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title_fullStr | Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title_full_unstemmed | Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title_short | Kinetic CRAC uncovers a role for Nab3 in determining gene expression profiles during stress |
title_sort | kinetic crac uncovers a role for nab3 in determining gene expression profiles during stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432031/ https://www.ncbi.nlm.nih.gov/pubmed/28400552 http://dx.doi.org/10.1038/s41467-017-00025-5 |
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