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Reconstruction of ancestral RNA sequences under multiple structural constraints
BACKGROUND: Secondary structures form the scaffold of multiple sequence alignment of non-coding RNA (ncRNA) families. An accurate reconstruction of ancestral ncRNAs must use this structural signal. However, the inference of ancestors of a single ncRNA family with a single consensus structure may bia...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123390/ https://www.ncbi.nlm.nih.gov/pubmed/28185557 http://dx.doi.org/10.1186/s12864-016-3105-4 |
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author | Tremblay-Savard, Olivier Reinharz, Vladimir Waldispühl, Jérôme |
author_facet | Tremblay-Savard, Olivier Reinharz, Vladimir Waldispühl, Jérôme |
author_sort | Tremblay-Savard, Olivier |
collection | PubMed |
description | BACKGROUND: Secondary structures form the scaffold of multiple sequence alignment of non-coding RNA (ncRNA) families. An accurate reconstruction of ancestral ncRNAs must use this structural signal. However, the inference of ancestors of a single ncRNA family with a single consensus structure may bias the results towards sequences with high affinity to this structure, which are far from the true ancestors. METHODS: In this paper, we introduce achARNement, a maximum parsimony approach that, given two alignments of homologous ncRNA families with consensus secondary structures and a phylogenetic tree, simultaneously calculates ancestral RNA sequences for these two families. RESULTS: We test our methodology on simulated data sets, and show that achARNement outperforms classical maximum parsimony approaches in terms of accuracy, but also reduces by several orders of magnitude the number of candidate sequences. To conclude this study, we apply our algorithms on the Glm clan and the FinP-traJ clan from the Rfam database. CONCLUSIONS: Our results show that our methods reconstruct small sets of high-quality candidate ancestors with better agreement to the two target structures than with classical approaches. Our program is freely available at: http://csb.cs.mcgill.ca/acharnement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3105-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5123390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51233902016-12-08 Reconstruction of ancestral RNA sequences under multiple structural constraints Tremblay-Savard, Olivier Reinharz, Vladimir Waldispühl, Jérôme BMC Genomics Research BACKGROUND: Secondary structures form the scaffold of multiple sequence alignment of non-coding RNA (ncRNA) families. An accurate reconstruction of ancestral ncRNAs must use this structural signal. However, the inference of ancestors of a single ncRNA family with a single consensus structure may bias the results towards sequences with high affinity to this structure, which are far from the true ancestors. METHODS: In this paper, we introduce achARNement, a maximum parsimony approach that, given two alignments of homologous ncRNA families with consensus secondary structures and a phylogenetic tree, simultaneously calculates ancestral RNA sequences for these two families. RESULTS: We test our methodology on simulated data sets, and show that achARNement outperforms classical maximum parsimony approaches in terms of accuracy, but also reduces by several orders of magnitude the number of candidate sequences. To conclude this study, we apply our algorithms on the Glm clan and the FinP-traJ clan from the Rfam database. CONCLUSIONS: Our results show that our methods reconstruct small sets of high-quality candidate ancestors with better agreement to the two target structures than with classical approaches. Our program is freely available at: http://csb.cs.mcgill.ca/acharnement. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3105-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-11 /pmc/articles/PMC5123390/ /pubmed/28185557 http://dx.doi.org/10.1186/s12864-016-3105-4 Text en © The Author(s) 2016 Open Access This 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 | Research Tremblay-Savard, Olivier Reinharz, Vladimir Waldispühl, Jérôme Reconstruction of ancestral RNA sequences under multiple structural constraints |
title | Reconstruction of ancestral RNA sequences under multiple structural constraints |
title_full | Reconstruction of ancestral RNA sequences under multiple structural constraints |
title_fullStr | Reconstruction of ancestral RNA sequences under multiple structural constraints |
title_full_unstemmed | Reconstruction of ancestral RNA sequences under multiple structural constraints |
title_short | Reconstruction of ancestral RNA sequences under multiple structural constraints |
title_sort | reconstruction of ancestral rna sequences under multiple structural constraints |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123390/ https://www.ncbi.nlm.nih.gov/pubmed/28185557 http://dx.doi.org/10.1186/s12864-016-3105-4 |
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