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Discovering sequence and structure landscapes in RNA interaction motifs
RNA molecules are able to bind proteins, DNA and other small or long RNAs using information at primary, secondary or tertiary structure level. Recent techniques that use cross-linking and immunoprecipitation of RNAs can detect these interactions and, if followed by high-throughput sequencing, molecu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547422/ https://www.ncbi.nlm.nih.gov/pubmed/31162604 http://dx.doi.org/10.1093/nar/gkz250 |
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author | Adinolfi, Marta Pietrosanto, Marco Parca, Luca Ausiello, Gabriele Ferrè, Fabrizio Helmer-Citterich, Manuela |
author_facet | Adinolfi, Marta Pietrosanto, Marco Parca, Luca Ausiello, Gabriele Ferrè, Fabrizio Helmer-Citterich, Manuela |
author_sort | Adinolfi, Marta |
collection | PubMed |
description | RNA molecules are able to bind proteins, DNA and other small or long RNAs using information at primary, secondary or tertiary structure level. Recent techniques that use cross-linking and immunoprecipitation of RNAs can detect these interactions and, if followed by high-throughput sequencing, molecules can be analysed to find recurrent elements shared by interactors, such as sequence and/or structure motifs. Many tools are able to find sequence motifs from lists of target RNAs, while others focus on structure using different approaches to find specific interaction elements. In this work, we make a systematic analysis of RBP–RNA and RNA–RNA datasets to better characterize the interaction landscape with information about multi-motifs on the same RNAs. To achieve this goal, we updated our BEAM algorithm to combine both sequence and structure information to create pairs of patterns that model motifs of interaction. This algorithm was applied to several RNA binding proteins and ncRNAs interactors, confirming already known motifs and discovering new ones. This landscape analysis on interaction variability reflects the diversity of target recognition and underlines that often both primary and secondary structure are involved in molecular recognition. |
format | Online Article Text |
id | pubmed-6547422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65474222019-06-13 Discovering sequence and structure landscapes in RNA interaction motifs Adinolfi, Marta Pietrosanto, Marco Parca, Luca Ausiello, Gabriele Ferrè, Fabrizio Helmer-Citterich, Manuela Nucleic Acids Res Computational Biology RNA molecules are able to bind proteins, DNA and other small or long RNAs using information at primary, secondary or tertiary structure level. Recent techniques that use cross-linking and immunoprecipitation of RNAs can detect these interactions and, if followed by high-throughput sequencing, molecules can be analysed to find recurrent elements shared by interactors, such as sequence and/or structure motifs. Many tools are able to find sequence motifs from lists of target RNAs, while others focus on structure using different approaches to find specific interaction elements. In this work, we make a systematic analysis of RBP–RNA and RNA–RNA datasets to better characterize the interaction landscape with information about multi-motifs on the same RNAs. To achieve this goal, we updated our BEAM algorithm to combine both sequence and structure information to create pairs of patterns that model motifs of interaction. This algorithm was applied to several RNA binding proteins and ncRNAs interactors, confirming already known motifs and discovering new ones. This landscape analysis on interaction variability reflects the diversity of target recognition and underlines that often both primary and secondary structure are involved in molecular recognition. Oxford University Press 2019-06-04 2019-04-10 /pmc/articles/PMC6547422/ /pubmed/31162604 http://dx.doi.org/10.1093/nar/gkz250 Text en © The Author(s) 2019. 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 Non-Commercial 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 Adinolfi, Marta Pietrosanto, Marco Parca, Luca Ausiello, Gabriele Ferrè, Fabrizio Helmer-Citterich, Manuela Discovering sequence and structure landscapes in RNA interaction motifs |
title | Discovering sequence and structure landscapes in RNA interaction motifs |
title_full | Discovering sequence and structure landscapes in RNA interaction motifs |
title_fullStr | Discovering sequence and structure landscapes in RNA interaction motifs |
title_full_unstemmed | Discovering sequence and structure landscapes in RNA interaction motifs |
title_short | Discovering sequence and structure landscapes in RNA interaction motifs |
title_sort | discovering sequence and structure landscapes in rna interaction motifs |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547422/ https://www.ncbi.nlm.nih.gov/pubmed/31162604 http://dx.doi.org/10.1093/nar/gkz250 |
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