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High-throughput characterization of protein–RNA interactions

RNA-binding proteins (RBPs) are important regulators of eukaryotic gene expression. Genomes typically encode dozens to hundreds of proteins containing RNA-binding domains, which collectively recognize diverse RNA sequences and structures. Recent advances in high-throughput methods for assaying the t...

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Detalles Bibliográficos
Autores principales: Cook, Kate B., Hughes, Timothy R., Morris, Quaid D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303715/
https://www.ncbi.nlm.nih.gov/pubmed/25504152
http://dx.doi.org/10.1093/bfgp/elu047
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author Cook, Kate B.
Hughes, Timothy R.
Morris, Quaid D.
author_facet Cook, Kate B.
Hughes, Timothy R.
Morris, Quaid D.
author_sort Cook, Kate B.
collection PubMed
description RNA-binding proteins (RBPs) are important regulators of eukaryotic gene expression. Genomes typically encode dozens to hundreds of proteins containing RNA-binding domains, which collectively recognize diverse RNA sequences and structures. Recent advances in high-throughput methods for assaying the targets of RBPs in vitro and in vivo allow large-scale derivation of RNA-binding motifs as well as determination of RNA–protein interactions in living cells. In parallel, many computational methods have been developed to analyze and interpret these data. The interplay between RNA secondary structure and RBP binding has also been a growing theme. Integrating RNA–protein interaction data with observations of post-transcriptional regulation will enhance our understanding of the roles of these important proteins.
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spelling pubmed-43037152015-02-24 High-throughput characterization of protein–RNA interactions Cook, Kate B. Hughes, Timothy R. Morris, Quaid D. Brief Funct Genomics Papers RNA-binding proteins (RBPs) are important regulators of eukaryotic gene expression. Genomes typically encode dozens to hundreds of proteins containing RNA-binding domains, which collectively recognize diverse RNA sequences and structures. Recent advances in high-throughput methods for assaying the targets of RBPs in vitro and in vivo allow large-scale derivation of RNA-binding motifs as well as determination of RNA–protein interactions in living cells. In parallel, many computational methods have been developed to analyze and interpret these data. The interplay between RNA secondary structure and RBP binding has also been a growing theme. Integrating RNA–protein interaction data with observations of post-transcriptional regulation will enhance our understanding of the roles of these important proteins. Oxford University Press 2015-01 2014-12-13 /pmc/articles/PMC4303715/ /pubmed/25504152 http://dx.doi.org/10.1093/bfgp/elu047 Text en © The Author 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Papers
Cook, Kate B.
Hughes, Timothy R.
Morris, Quaid D.
High-throughput characterization of protein–RNA interactions
title High-throughput characterization of protein–RNA interactions
title_full High-throughput characterization of protein–RNA interactions
title_fullStr High-throughput characterization of protein–RNA interactions
title_full_unstemmed High-throughput characterization of protein–RNA interactions
title_short High-throughput characterization of protein–RNA interactions
title_sort high-throughput characterization of protein–rna interactions
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303715/
https://www.ncbi.nlm.nih.gov/pubmed/25504152
http://dx.doi.org/10.1093/bfgp/elu047
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