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The SMAD3 transcription factor binds complex RNA structures with high affinity

Several members of the SMAD family of transcription factors have been reported to bind RNA in addition to their canonical double-stranded DNA (dsDNA) ligand. RNA binding by SMAD has the potential to affect numerous cellular functions that involve RNA. However, the affinity and specificity of this RN...

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Detalles Bibliográficos
Autores principales: Dickey, Thayne H., Pyle, Anna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714123/
https://www.ncbi.nlm.nih.gov/pubmed/29036649
http://dx.doi.org/10.1093/nar/gkx846
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author Dickey, Thayne H.
Pyle, Anna M.
author_facet Dickey, Thayne H.
Pyle, Anna M.
author_sort Dickey, Thayne H.
collection PubMed
description Several members of the SMAD family of transcription factors have been reported to bind RNA in addition to their canonical double-stranded DNA (dsDNA) ligand. RNA binding by SMAD has the potential to affect numerous cellular functions that involve RNA. However, the affinity and specificity of this RNA binding activity has not been well characterized, which limits the ability to validate and extrapolate functional implications of this activity. Here we perform quantitative binding experiments in vitro to determine the ligand requirements for RNA binding by SMAD3. We find that SMAD3 binds poorly to single- and double-stranded RNA, regardless of sequence. However, SMAD3 binds RNA with large internal loops or bulges with high apparent affinity. This apparent affinity matches that for its canonical dsDNA ligand, suggesting a biological role for RNA binding by SMAD3.
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spelling pubmed-57141232017-12-08 The SMAD3 transcription factor binds complex RNA structures with high affinity Dickey, Thayne H. Pyle, Anna M. Nucleic Acids Res RNA and RNA-protein complexes Several members of the SMAD family of transcription factors have been reported to bind RNA in addition to their canonical double-stranded DNA (dsDNA) ligand. RNA binding by SMAD has the potential to affect numerous cellular functions that involve RNA. However, the affinity and specificity of this RNA binding activity has not been well characterized, which limits the ability to validate and extrapolate functional implications of this activity. Here we perform quantitative binding experiments in vitro to determine the ligand requirements for RNA binding by SMAD3. We find that SMAD3 binds poorly to single- and double-stranded RNA, regardless of sequence. However, SMAD3 binds RNA with large internal loops or bulges with high apparent affinity. This apparent affinity matches that for its canonical dsDNA ligand, suggesting a biological role for RNA binding by SMAD3. Oxford University Press 2017-11-16 2017-09-25 /pmc/articles/PMC5714123/ /pubmed/29036649 http://dx.doi.org/10.1093/nar/gkx846 Text en © The Author(s) 2017. 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 and RNA-protein complexes
Dickey, Thayne H.
Pyle, Anna M.
The SMAD3 transcription factor binds complex RNA structures with high affinity
title The SMAD3 transcription factor binds complex RNA structures with high affinity
title_full The SMAD3 transcription factor binds complex RNA structures with high affinity
title_fullStr The SMAD3 transcription factor binds complex RNA structures with high affinity
title_full_unstemmed The SMAD3 transcription factor binds complex RNA structures with high affinity
title_short The SMAD3 transcription factor binds complex RNA structures with high affinity
title_sort smad3 transcription factor binds complex rna structures with high affinity
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714123/
https://www.ncbi.nlm.nih.gov/pubmed/29036649
http://dx.doi.org/10.1093/nar/gkx846
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