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A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications

Functional RNA regions are often related to recurrent secondary structure patterns (or motifs), which can exert their role in several different ways, particularly in dictating the interaction with RNA-binding proteins, and acting in the regulation of a large number of cellular processes. Among the a...

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Autores principales: Pietrosanto, Marco, Mattei, Eugenio, Helmer-Citterich, Manuela, Ferrè, Fabrizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062999/
https://www.ncbi.nlm.nih.gov/pubmed/27580722
http://dx.doi.org/10.1093/nar/gkw750
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author Pietrosanto, Marco
Mattei, Eugenio
Helmer-Citterich, Manuela
Ferrè, Fabrizio
author_facet Pietrosanto, Marco
Mattei, Eugenio
Helmer-Citterich, Manuela
Ferrè, Fabrizio
author_sort Pietrosanto, Marco
collection PubMed
description Functional RNA regions are often related to recurrent secondary structure patterns (or motifs), which can exert their role in several different ways, particularly in dictating the interaction with RNA-binding proteins, and acting in the regulation of a large number of cellular processes. Among the available motif-finding tools, the majority focuses on sequence patterns, sometimes including secondary structure as additional constraints to improve their performance. Nonetheless, secondary structures motifs may be concurrent to their sequence counterparts or even encode a stronger functional signal. Current methods for searching structural motifs generally require long pipelines and/or high computational efforts or previously aligned sequences. Here, we present BEAM (BEAr Motif finder), a novel method for structural motif discovery from a set of unaligned RNAs, taking advantage of a recently developed encoding for RNA secondary structure named BEAR (Brand nEw Alphabet for RNAs) and of evolutionary substitution rates of secondary structure elements. Tested in a varied set of scenarios, from small- to large-scale, BEAM is successful in retrieving structural motifs even in highly noisy data sets, such as those that can arise in CLIP-Seq or other high-throughput experiments.
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spelling pubmed-50629992016-10-14 A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications Pietrosanto, Marco Mattei, Eugenio Helmer-Citterich, Manuela Ferrè, Fabrizio Nucleic Acids Res Computational Biology Functional RNA regions are often related to recurrent secondary structure patterns (or motifs), which can exert their role in several different ways, particularly in dictating the interaction with RNA-binding proteins, and acting in the regulation of a large number of cellular processes. Among the available motif-finding tools, the majority focuses on sequence patterns, sometimes including secondary structure as additional constraints to improve their performance. Nonetheless, secondary structures motifs may be concurrent to their sequence counterparts or even encode a stronger functional signal. Current methods for searching structural motifs generally require long pipelines and/or high computational efforts or previously aligned sequences. Here, we present BEAM (BEAr Motif finder), a novel method for structural motif discovery from a set of unaligned RNAs, taking advantage of a recently developed encoding for RNA secondary structure named BEAR (Brand nEw Alphabet for RNAs) and of evolutionary substitution rates of secondary structure elements. Tested in a varied set of scenarios, from small- to large-scale, BEAM is successful in retrieving structural motifs even in highly noisy data sets, such as those that can arise in CLIP-Seq or other high-throughput experiments. Oxford University Press 2016-10-14 2016-08-31 /pmc/articles/PMC5062999/ /pubmed/27580722 http://dx.doi.org/10.1093/nar/gkw750 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Computational Biology
Pietrosanto, Marco
Mattei, Eugenio
Helmer-Citterich, Manuela
Ferrè, Fabrizio
A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title_full A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title_fullStr A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title_full_unstemmed A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title_short A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
title_sort novel method for the identification of conserved structural patterns in rna: from small scale to high-throughput applications
topic Computational Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062999/
https://www.ncbi.nlm.nih.gov/pubmed/27580722
http://dx.doi.org/10.1093/nar/gkw750
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