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dc.contributor.authorFARES, MARIOen
dc.date.accessioned2017-03-27T10:54:41Z
dc.date.available2017-03-27T10:54:41Z
dc.date.created2015en
dc.date.issued2015en
dc.date.submitted2015en
dc.identifier.citationLuisi P, Alvarez-Ponce D, Pybus M, Fares M.A, Bertranpetit J, Laayouni H, Recent positive selection has acted on genes encoding proteins with more interactions within the whole human interactome, Genome Biology and Evolution, 7, 4, 2015, 1141 - 1154en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.descriptionCited By :6 Export Date: 23 March 2017en
dc.description.abstractGenes vary in their likelihood to undergo adaptive evolution. The genomic factors that determine adaptability, however, remain poorly understood. Genes function in the context of molecular networks, with some occupying more important positions than others and thus being likely to be under stronger selective pressures. However, how positive selection distributes across the different parts of molecular networks is still not fully understood. Here, we inferred positive selection using comparative genomics and population genetics approaches through the comparison of 10 mammalian and 270 human genomes, respectively. In agreement with previous results, we found that genes with lower network centralities are more likely to evolve under positive selection (as inferred from divergence data). Surprisingly, polymorphism data yield results in the opposite direction than divergence data: Genes with higher centralities are more likely to have been targeted by recent positive selection during recent human evolution. Our results indicate that the relationship between centrality and the impact of adaptive evolution highly depends on the mode of positive selection and/or the evolutionary time-scale.en
dc.description.sponsorshipThe authors thankfully acknowledge valuable discussion and corrections from Diego A. Hartasanchez, David A. Hughes, Jessica Nye, and Arcadi Navarro. They thank Gabriel Santpere for his help to compute the McDonald–Krietman test. They also thank the National Institute of Bioinformatics (http://www.inab.org) and Javier Forment, from the Bioinformatics service at the “Instituto de Biología Molecular y Celular de Plantas,” for computational support. This work was funded by the “Ministerio de Ciencia y Tecnología” (Spain) (grant BFU2013-43726-P), and the “Direcció General de Recerca, Generalitat de Catalunya (Grup de Recerca Consolidat 2009 SGR 1101)” awarded to J.B. P.L. was supported by a Ph.D. fellowship from “Acción Estratégica de Salud, en el marco del Plan Nacional de Investigación Científica, Desarrollo e Innovación Tecnológica 2008–2011” from Instituto de Salud Carlos III. D.A.-P. was a “Juan de la Cierva” fellow from the “Ministerio de Economía y Competitividad” (Spain) (JCI-2011-11089). M.A.F. was supported by a Principal Investigator grant from Science Foundation Ireland (12/IP/1673) and a project from the “Ministerio de Economía y Competitividad” (grant number BFU2012-36346).en
dc.format.extent1141en
dc.format.extent1154en
dc.relation.ispartofseriesGenome Biology and Evolutionen
dc.relation.ispartofseries7en
dc.relation.ispartofseries4en
dc.rightsYen
dc.subjectphysical protein interaction, protein interaction network, natural selection, positive selection, mammals, humansen
dc.subject.lcshphysical protein interaction, protein interaction network, natural selection, positive selection, mammals, humansen
dc.titleRecent positive selection has acted on genes encoding proteins with more interactions within the whole human interactomeen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/faresmen
dc.identifier.rssinternalid155447en
dc.identifier.doihttp://dx.doi.org/10.1093/gbe/evv055en
dc.rights.ecaccessrightsopenAccess
dc.identifier.rssurihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84942279654&doi=10.1093%2fgbe%2fevv055&partnerID=40&md5=8c97db822d734ae01aa9497c3df04197en
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.contributor.sponsorGrantNumber12/IP/1673en
dc.identifier.urihttp://hdl.handle.net/2262/79694


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