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Nucleic acid-binding specificity of human FUS protein

FUS, a nuclear RNA-binding protein, plays multiple roles in RNA processing. Five specific FUS-binding RNA sequence/structure motifs have been proposed, but their affinities for FUS have not been directly compared. Here we find that human FUS binds all these sequences with K(d)(app) values spanning a...

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Detalles Bibliográficos
Autores principales: Wang, Xueyin, Schwartz, Jacob C., Cech, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551922/
https://www.ncbi.nlm.nih.gov/pubmed/26150427
http://dx.doi.org/10.1093/nar/gkv679
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author Wang, Xueyin
Schwartz, Jacob C.
Cech, Thomas R.
author_facet Wang, Xueyin
Schwartz, Jacob C.
Cech, Thomas R.
author_sort Wang, Xueyin
collection PubMed
description FUS, a nuclear RNA-binding protein, plays multiple roles in RNA processing. Five specific FUS-binding RNA sequence/structure motifs have been proposed, but their affinities for FUS have not been directly compared. Here we find that human FUS binds all these sequences with K(d)(app) values spanning a 10-fold range. Furthermore, some RNAs that do not contain any of these motifs bind FUS with similar affinity. FUS binds RNA in a length-dependent manner, consistent with a substantial non-specific component to binding. Finally, investigation of FUS binding to different nucleic acids shows that it binds single-stranded DNA with three-fold lower affinity than ssRNA of the same length and sequence, while binding to double-stranded nucleic acids is weaker. We conclude that FUS has quite general nucleic acid-binding activity, with the various proposed RNA motifs being neither necessary for FUS binding nor sufficient to explain its diverse binding partners.
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spelling pubmed-45519222015-08-28 Nucleic acid-binding specificity of human FUS protein Wang, Xueyin Schwartz, Jacob C. Cech, Thomas R. Nucleic Acids Res RNA FUS, a nuclear RNA-binding protein, plays multiple roles in RNA processing. Five specific FUS-binding RNA sequence/structure motifs have been proposed, but their affinities for FUS have not been directly compared. Here we find that human FUS binds all these sequences with K(d)(app) values spanning a 10-fold range. Furthermore, some RNAs that do not contain any of these motifs bind FUS with similar affinity. FUS binds RNA in a length-dependent manner, consistent with a substantial non-specific component to binding. Finally, investigation of FUS binding to different nucleic acids shows that it binds single-stranded DNA with three-fold lower affinity than ssRNA of the same length and sequence, while binding to double-stranded nucleic acids is weaker. We conclude that FUS has quite general nucleic acid-binding activity, with the various proposed RNA motifs being neither necessary for FUS binding nor sufficient to explain its diverse binding partners. Oxford University Press 2015-09-03 2015-07-06 /pmc/articles/PMC4551922/ /pubmed/26150427 http://dx.doi.org/10.1093/nar/gkv679 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 RNA
Wang, Xueyin
Schwartz, Jacob C.
Cech, Thomas R.
Nucleic acid-binding specificity of human FUS protein
title Nucleic acid-binding specificity of human FUS protein
title_full Nucleic acid-binding specificity of human FUS protein
title_fullStr Nucleic acid-binding specificity of human FUS protein
title_full_unstemmed Nucleic acid-binding specificity of human FUS protein
title_short Nucleic acid-binding specificity of human FUS protein
title_sort nucleic acid-binding specificity of human fus protein
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551922/
https://www.ncbi.nlm.nih.gov/pubmed/26150427
http://dx.doi.org/10.1093/nar/gkv679
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