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dc.contributor.authorYoder, ADen_US
dc.contributor.authorChan, LMen_US
dc.contributor.authordos Reis, Men_US
dc.contributor.authorLarsen, PAen_US
dc.contributor.authorCampbell, CRen_US
dc.contributor.authorRasoloarison, Ren_US
dc.contributor.authorBarrett, Men_US
dc.contributor.authorRoos, Cen_US
dc.contributor.authorKappeler, Pen_US
dc.contributor.authorBielawski, Jen_US
dc.contributor.authorYang, Zen_US
dc.date.accessioned2016-05-13T09:58:37Z
dc.date.issued2014-01en_US
dc.date.submitted2016-05-04T17:18:51.222Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/12307
dc.description.abstractVomeronasal receptor genes have frequently been invoked as integral to the establishment and maintenance of species boundaries among mammals due to the elaborate one-to-one correspondence between semiochemical signals and neuronal sensory inputs. Here, we report the most extensive sample of vomeronasal receptor class 1 (V1R) sequences ever generated for a diverse yet phylogenetically coherent group of mammals, the tooth-combed primates (suborder Strepsirrhini). Phylogenetic analysis confirms our intensive sampling from a single V1R subfamily, apparently unique to the strepsirrhine primates. We designate this subfamily as V1Rstrep. The subfamily retains extensive repertoires of gene copies that descend from an ancestral gene duplication that appears to have occurred prior to the diversification of all lemuriform primates excluding the basal genus Daubentonia (the aye-aye). We refer to the descendent clades as V1Rstrep-α and V1Rstrep-β. Comparison of the two clades reveals different amino acid compositions corresponding to the predicted ligand-binding site and thus potentially to altered functional profiles between the two. In agreement with previous studies of the mouse lemur (genus, Microcebus), the majority of V1Rstrep gene copies appear to be intact and under strong positive selection, particularly within transmembrane regions. Finally, despite the surprisingly high number of gene copies identified in this study, it is nonetheless probable that V1R diversity remains underestimated in these nonmodel primates and that complete characterization will be limited until high-coverage assembled genomes are available.en_US
dc.format.extent213 - 227en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofGenome Biol Evolen_US
dc.rightsCC-BY
dc.subjectG-protein-coupled receptorsen_US
dc.subjectchemosensory genesen_US
dc.subjectgene family evolutionen_US
dc.subjectlemursen_US
dc.subjectolfactionen_US
dc.subjectpositive selectionen_US
dc.subjectAmino Acid Sequenceen_US
dc.subjectAnimalsen_US
dc.subjectBase Sequenceen_US
dc.subjectEvolution, Molecularen_US
dc.subjectGene Dosageen_US
dc.subjectGene Duplicationen_US
dc.subjectMolecular Sequence Dataen_US
dc.subjectMultigene Familyen_US
dc.subjectPhylogenyen_US
dc.subjectProtein Structure, Tertiaryen_US
dc.subjectReceptors, G-Protein-Coupleden_US
dc.subjectStrepsirhinien_US
dc.subjectVomeronasal Organen_US
dc.titleMolecular evolutionary characterization of a V1R subfamily unique to strepsirrhine primates.en_US
dc.typeArticle
dc.rights.holder© 2014 The Author(s)
dc.identifier.doi10.1093/gbe/evu006en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/24398377en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume6en_US


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