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Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals
In mammals, social and sexual behaviours are largely mediated by the vomeronasal system (VNS). The accessory olfactory bulb (AOB) is the first synaptic locus of the VNS and ranges from very large in Caviomorph rodents, small in carnivores and ungulates, to its complete absence in apes, elephants, mo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198400/ https://www.ncbi.nlm.nih.gov/pubmed/22039487 http://dx.doi.org/10.1371/journal.pone.0026436 |
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author | Suárez, Rodrigo Fernández-Aburto, Pedro Manger, Paul R. Mpodozis, Jorge |
author_facet | Suárez, Rodrigo Fernández-Aburto, Pedro Manger, Paul R. Mpodozis, Jorge |
author_sort | Suárez, Rodrigo |
collection | PubMed |
description | In mammals, social and sexual behaviours are largely mediated by the vomeronasal system (VNS). The accessory olfactory bulb (AOB) is the first synaptic locus of the VNS and ranges from very large in Caviomorph rodents, small in carnivores and ungulates, to its complete absence in apes, elephants, most bats and aquatic species. Two pathways have been described in the VNS of mammals. In mice, vomeronasal neurons expressing Gαi2 protein project to the rostral portion of the AOB and respond mostly to small volatile molecules, whereas neurons expressing Gαo project to the caudal AOB and respond mostly to large non-volatile molecules. However, the Gαo-expressing pathway is absent in several species (horses, dogs, musk shrews, goats and marmosets) but no hypotheses have been proposed to date to explain the loss of that pathway. We noted that the species that lost the Gαo pathway belong to Laurasiatheria and Primates lineages, both clades with ubiquitous sexual dimorphisms across species. To assess whether similar events of Gαo pathway loss could have occurred convergently in dimorphic species we studied G-protein expression in the AOB of two species that independently evolved sexually dimorphic traits: the California ground squirrel Spermophilus beecheyi (Rodentia; Sciurognathi) and the cape hyrax Procavia capensis (Afrotheria; Hyracoidea). We found that both species show uniform expression of Gαi2-protein throughout AOB glomeruli, while Gαo expression is restricted to main olfactory glomeruli only. Our results suggest that the degeneration of the Gαo-expressing vomeronasal pathway has occurred independently at least four times in Eutheria, possibly related to the emergence of sexual dimorphisms and the ability of detecting the gender of conspecifics at distance. |
format | Online Article Text |
id | pubmed-3198400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31984002011-10-28 Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals Suárez, Rodrigo Fernández-Aburto, Pedro Manger, Paul R. Mpodozis, Jorge PLoS One Research Article In mammals, social and sexual behaviours are largely mediated by the vomeronasal system (VNS). The accessory olfactory bulb (AOB) is the first synaptic locus of the VNS and ranges from very large in Caviomorph rodents, small in carnivores and ungulates, to its complete absence in apes, elephants, most bats and aquatic species. Two pathways have been described in the VNS of mammals. In mice, vomeronasal neurons expressing Gαi2 protein project to the rostral portion of the AOB and respond mostly to small volatile molecules, whereas neurons expressing Gαo project to the caudal AOB and respond mostly to large non-volatile molecules. However, the Gαo-expressing pathway is absent in several species (horses, dogs, musk shrews, goats and marmosets) but no hypotheses have been proposed to date to explain the loss of that pathway. We noted that the species that lost the Gαo pathway belong to Laurasiatheria and Primates lineages, both clades with ubiquitous sexual dimorphisms across species. To assess whether similar events of Gαo pathway loss could have occurred convergently in dimorphic species we studied G-protein expression in the AOB of two species that independently evolved sexually dimorphic traits: the California ground squirrel Spermophilus beecheyi (Rodentia; Sciurognathi) and the cape hyrax Procavia capensis (Afrotheria; Hyracoidea). We found that both species show uniform expression of Gαi2-protein throughout AOB glomeruli, while Gαo expression is restricted to main olfactory glomeruli only. Our results suggest that the degeneration of the Gαo-expressing vomeronasal pathway has occurred independently at least four times in Eutheria, possibly related to the emergence of sexual dimorphisms and the ability of detecting the gender of conspecifics at distance. Public Library of Science 2011-10-19 /pmc/articles/PMC3198400/ /pubmed/22039487 http://dx.doi.org/10.1371/journal.pone.0026436 Text en Suárez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Suárez, Rodrigo Fernández-Aburto, Pedro Manger, Paul R. Mpodozis, Jorge Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title | Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title_full | Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title_fullStr | Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title_full_unstemmed | Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title_short | Deterioration of the Gαo Vomeronasal Pathway in Sexually Dimorphic Mammals |
title_sort | deterioration of the gαo vomeronasal pathway in sexually dimorphic mammals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198400/ https://www.ncbi.nlm.nih.gov/pubmed/22039487 http://dx.doi.org/10.1371/journal.pone.0026436 |
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