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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),...

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Autores principales: van Nues, Rob, Schweikert, Gabriele, de Leau, Erica, Selega, Alina, Langford, Andrew, Franklin, Ryan, Iosub, Ira, Wadsworth, Peter, Sanguinetti, Guido, Granneman, Sander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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