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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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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. |
format | Online Article Text |
id | pubmed-5062999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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