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Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity

Specificity of RNA-binding proteins for target sequences varies considerably. Yet, it is not understood how certain few proteins achieve markedly higher sequence specificity than most others. Here we show that the RNA Recognition Motif of RbFox accomplishes extraordinary sequence specificity by empl...

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Autores principales: Ye, Xuan, Yang, Wen, Yi, Soon, Zhao, Yanan, Varani, Gabriele, Jankowsky, Eckhard, Yang, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911399/
https://www.ncbi.nlm.nih.gov/pubmed/36759600
http://dx.doi.org/10.1038/s41467-023-36394-3
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author Ye, Xuan
Yang, Wen
Yi, Soon
Zhao, Yanan
Varani, Gabriele
Jankowsky, Eckhard
Yang, Fan
author_facet Ye, Xuan
Yang, Wen
Yi, Soon
Zhao, Yanan
Varani, Gabriele
Jankowsky, Eckhard
Yang, Fan
author_sort Ye, Xuan
collection PubMed
description Specificity of RNA-binding proteins for target sequences varies considerably. Yet, it is not understood how certain few proteins achieve markedly higher sequence specificity than most others. Here we show that the RNA Recognition Motif of RbFox accomplishes extraordinary sequence specificity by employing functionally and structurally distinct binding modes. Affinity measurements of RbFox for all binding site variants reveal the existence of two distinct binding modes. The first exclusively accommodates cognate and closely related RNAs with high affinity. The second mode accommodates all other RNAs with reduced affinity by imposing large thermodynamic penalties on non-cognate sequences. NMR studies indicate marked structural differences between the two binding modes, including large conformational rearrangements distant from the RNA-binding site. Distinct binding modes by a single RNA-binding module explain extraordinary sequence selectivity and reveal an unknown layer of functional diversity, cross talk and regulation in RNA-protein interactions.
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spelling pubmed-99113992023-02-11 Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity Ye, Xuan Yang, Wen Yi, Soon Zhao, Yanan Varani, Gabriele Jankowsky, Eckhard Yang, Fan Nat Commun Article Specificity of RNA-binding proteins for target sequences varies considerably. Yet, it is not understood how certain few proteins achieve markedly higher sequence specificity than most others. Here we show that the RNA Recognition Motif of RbFox accomplishes extraordinary sequence specificity by employing functionally and structurally distinct binding modes. Affinity measurements of RbFox for all binding site variants reveal the existence of two distinct binding modes. The first exclusively accommodates cognate and closely related RNAs with high affinity. The second mode accommodates all other RNAs with reduced affinity by imposing large thermodynamic penalties on non-cognate sequences. NMR studies indicate marked structural differences between the two binding modes, including large conformational rearrangements distant from the RNA-binding site. Distinct binding modes by a single RNA-binding module explain extraordinary sequence selectivity and reveal an unknown layer of functional diversity, cross talk and regulation in RNA-protein interactions. Nature Publishing Group UK 2023-02-09 /pmc/articles/PMC9911399/ /pubmed/36759600 http://dx.doi.org/10.1038/s41467-023-36394-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ye, Xuan
Yang, Wen
Yi, Soon
Zhao, Yanan
Varani, Gabriele
Jankowsky, Eckhard
Yang, Fan
Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title_full Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title_fullStr Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title_full_unstemmed Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title_short Two distinct binding modes provide the RNA-binding protein RbFox with extraordinary sequence specificity
title_sort two distinct binding modes provide the rna-binding protein rbfox with extraordinary sequence specificity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911399/
https://www.ncbi.nlm.nih.gov/pubmed/36759600
http://dx.doi.org/10.1038/s41467-023-36394-3
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