dc.contributor.author
Mengual Chuliá, Beatriz
dc.contributor.author
Bedhomme, Stéphanie
dc.contributor.author
Lafforgue, Guillaume
dc.contributor.author
Elena, Santiago F.
dc.contributor.author
Bravo, Ignacio G.
dc.date.issued
2018-12-11T11:28:20Z
dc.date.issued
2018-12-11T11:28:20Z
dc.date.issued
2016-02-05
dc.date.issued
2018-07-25T07:52:26Z
dc.identifier
https://hdl.handle.net/2445/126884
dc.description.abstract
Background: The increasing abundance of sequence data has exacerbated a long known problem: gene trees and species trees for the same terminal taxa are often incongruent. Indeed, genes within a genome have not all followed the same evolutionary path due to events such as incomplete lineage sorting, horizontal gene transfer, gene duplication and deletion, or recombination. Considering conflicts between gene trees as an obstacle, numerous methods have been developed to deal with these incongruences and to reconstruct consensus evolutionary histories of species despite the heterogeneity in the history of their genes. However, inconsistencies can also be seen as a source of information about the specific evolutionary processes that have shaped genomes. Results: The goal of the approach here proposed is to exploit this conflicting information: we have compiled eleven variables describing phylogenetic relationships and evolutionary pressures and submitted them to dimensionality reduction techniques to identify genes with similar evolutionary histories. To illustrate the applicability of the method, we have chosen two viral datasets, namely papillomaviruses and Turnip mosaic virus (TuMV) isolates, largely dissimilar in genome, evolutionary distance and biology. Our method pinpoints viral genes with common evolutionary patterns. In the case of papillomaviruses, gene clusters match well our knowledge on viral biology and life cycle, illustrating the potential of our approach. For the less known TuMV, our results trigger new hypotheses about viral evolution and gene interaction. Conclusions: The approach here presented allows turning phylogenetic inconsistencies into evolutionary information, detecting gene assemblies with similar histories, and could be a powerful tool for comparative pathogenomics.
dc.format
application/pdf
dc.format
application/pdf
dc.publisher
BioMed Central
dc.relation
Reproducció del document publicat a: https://doi.org/10.1186/s12862-016-0605-4
dc.relation
BMC Evolutionary Biology, 2016, vol. 16, num. 32
dc.relation
https://doi.org/10.1186/s12862-016-0605-4
dc.rights
cc by (c) Mengual Chuliá et al., 2016
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Papil·lomavirus
dc.subject
Papillomaviruses
dc.title
Assessing parallel gene histories in viral
genomes
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion