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New in silico approach to assessing RNA secondary structures with non-canonical base pairs

BACKGROUND: The function of RNA is strongly dependent on its structure, so an appropriate recognition of this structure, on every level of organization, is of great importance. One particular concern is the assessment of base-base interactions, described as the secondary structure, the knowledge of...

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Autores principales: Rybarczyk, Agnieszka, Szostak, Natalia, Antczak, Maciej, Zok, Tomasz, Popenda, Mariusz, Adamiak, Ryszard, Blazewicz, Jacek, Szachniuk, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557229/
https://www.ncbi.nlm.nih.gov/pubmed/26329823
http://dx.doi.org/10.1186/s12859-015-0718-6
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author Rybarczyk, Agnieszka
Szostak, Natalia
Antczak, Maciej
Zok, Tomasz
Popenda, Mariusz
Adamiak, Ryszard
Blazewicz, Jacek
Szachniuk, Marta
author_facet Rybarczyk, Agnieszka
Szostak, Natalia
Antczak, Maciej
Zok, Tomasz
Popenda, Mariusz
Adamiak, Ryszard
Blazewicz, Jacek
Szachniuk, Marta
author_sort Rybarczyk, Agnieszka
collection PubMed
description BACKGROUND: The function of RNA is strongly dependent on its structure, so an appropriate recognition of this structure, on every level of organization, is of great importance. One particular concern is the assessment of base-base interactions, described as the secondary structure, the knowledge of which greatly facilitates an interpretation of RNA function and allows for structure analysis on the tertiary level. The RNA secondary structure can be predicted from a sequence using in silico methods often adjusted with experimental data, or assessed from 3D structure atom coordinates. Computational approaches typically consider only canonical, Watson-Crick and wobble base pairs. Handling of non-canonical interactions, important for a full description of RNA structure, is still very difficult. RESULTS: We introduce our novel approach to assessing an extended RNA secondary structure, which characterizes both canonical and non-canonical base pairs, along with their type classification. It is based on predicting the RNA 3D structure from a user-provided sequence or a secondary structure that only describes canonical base pairs, and then deriving the extended secondary structure from atom coordinates. In our example implementation, this was achieved by integrating the functionality of two fully automated, high fidelity methods in a computational pipeline: RNAComposer for the 3D RNA structure prediction and RNApdbee for base-pair annotation. CONCLUSIONS: The presented methodology ties together existing applications for RNA 3D structure prediction and base-pair annotation. The example performance, applying RNAComposer and RNApdbee, reveals better accuracy in non-canonical base pair assessment than the compared methods that directly predict RNA secondary structure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0718-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-45572292015-09-03 New in silico approach to assessing RNA secondary structures with non-canonical base pairs Rybarczyk, Agnieszka Szostak, Natalia Antczak, Maciej Zok, Tomasz Popenda, Mariusz Adamiak, Ryszard Blazewicz, Jacek Szachniuk, Marta BMC Bioinformatics Methodology Article BACKGROUND: The function of RNA is strongly dependent on its structure, so an appropriate recognition of this structure, on every level of organization, is of great importance. One particular concern is the assessment of base-base interactions, described as the secondary structure, the knowledge of which greatly facilitates an interpretation of RNA function and allows for structure analysis on the tertiary level. The RNA secondary structure can be predicted from a sequence using in silico methods often adjusted with experimental data, or assessed from 3D structure atom coordinates. Computational approaches typically consider only canonical, Watson-Crick and wobble base pairs. Handling of non-canonical interactions, important for a full description of RNA structure, is still very difficult. RESULTS: We introduce our novel approach to assessing an extended RNA secondary structure, which characterizes both canonical and non-canonical base pairs, along with their type classification. It is based on predicting the RNA 3D structure from a user-provided sequence or a secondary structure that only describes canonical base pairs, and then deriving the extended secondary structure from atom coordinates. In our example implementation, this was achieved by integrating the functionality of two fully automated, high fidelity methods in a computational pipeline: RNAComposer for the 3D RNA structure prediction and RNApdbee for base-pair annotation. CONCLUSIONS: The presented methodology ties together existing applications for RNA 3D structure prediction and base-pair annotation. The example performance, applying RNAComposer and RNApdbee, reveals better accuracy in non-canonical base pair assessment than the compared methods that directly predict RNA secondary structure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0718-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-02 /pmc/articles/PMC4557229/ /pubmed/26329823 http://dx.doi.org/10.1186/s12859-015-0718-6 Text en © Rybarczyk et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Rybarczyk, Agnieszka
Szostak, Natalia
Antczak, Maciej
Zok, Tomasz
Popenda, Mariusz
Adamiak, Ryszard
Blazewicz, Jacek
Szachniuk, Marta
New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title_full New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title_fullStr New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title_full_unstemmed New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title_short New in silico approach to assessing RNA secondary structures with non-canonical base pairs
title_sort new in silico approach to assessing rna secondary structures with non-canonical base pairs
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557229/
https://www.ncbi.nlm.nih.gov/pubmed/26329823
http://dx.doi.org/10.1186/s12859-015-0718-6
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