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A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo

BACKGROUND: Optimal reproductive fitness is essential for the biological success and survival of species. The vomeronasal organ is strongly implicated in the display of sexual and reproductive behaviors in female mice, yet the roles that apical and basal vomeronasal neuron populations play in contro...

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Autores principales: Oboti, Livio, Pérez-Gómez, Anabel, Keller, Matthieu, Jacobi, Eric, Birnbaumer, Lutz, Leinders-Zufall, Trese, Zufall, Frank, Chamero, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038847/
https://www.ncbi.nlm.nih.gov/pubmed/24886577
http://dx.doi.org/10.1186/1741-7007-12-31
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author Oboti, Livio
Pérez-Gómez, Anabel
Keller, Matthieu
Jacobi, Eric
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
author_facet Oboti, Livio
Pérez-Gómez, Anabel
Keller, Matthieu
Jacobi, Eric
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
author_sort Oboti, Livio
collection PubMed
description BACKGROUND: Optimal reproductive fitness is essential for the biological success and survival of species. The vomeronasal organ is strongly implicated in the display of sexual and reproductive behaviors in female mice, yet the roles that apical and basal vomeronasal neuron populations play in controlling these gender-specific behaviors remain largely unclear. RESULTS: To dissect the neural pathways underlying these functions, we genetically inactivated the basal vomeronasal organ layer using conditional, cell-specific ablation of the G protein Gαo. Female mice mutant for Gαo show severe alterations in sexual and reproductive behaviors, timing of puberty onset, and estrous cycle. These mutant mice are insensitive to reproductive facilitation stimulated by male pheromones that accelerate puberty and induce ovulation. Gαo-mutant females exhibit a striking reduction in sexual receptivity or lordosis behavior to males, but gender discrimination seems to be intact. These mice also show a loss in male scent preference, which requires a learned association for volatile olfactory signals with other nonvolatile ownership signals that are contained in the high molecular weight fraction of male urine. Thus, Gαo impacts on both instinctive and learned social responses to pheromones. CONCLUSIONS: These results highlight that sensory neurons of the Gαo-expressing vomeronasal subsystem, together with the receptors they express and the molecular cues they detect, control a wide range of fundamental mating and reproductive behaviors in female mice.
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spelling pubmed-40388472014-05-31 A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo Oboti, Livio Pérez-Gómez, Anabel Keller, Matthieu Jacobi, Eric Birnbaumer, Lutz Leinders-Zufall, Trese Zufall, Frank Chamero, Pablo BMC Biol Research Article BACKGROUND: Optimal reproductive fitness is essential for the biological success and survival of species. The vomeronasal organ is strongly implicated in the display of sexual and reproductive behaviors in female mice, yet the roles that apical and basal vomeronasal neuron populations play in controlling these gender-specific behaviors remain largely unclear. RESULTS: To dissect the neural pathways underlying these functions, we genetically inactivated the basal vomeronasal organ layer using conditional, cell-specific ablation of the G protein Gαo. Female mice mutant for Gαo show severe alterations in sexual and reproductive behaviors, timing of puberty onset, and estrous cycle. These mutant mice are insensitive to reproductive facilitation stimulated by male pheromones that accelerate puberty and induce ovulation. Gαo-mutant females exhibit a striking reduction in sexual receptivity or lordosis behavior to males, but gender discrimination seems to be intact. These mice also show a loss in male scent preference, which requires a learned association for volatile olfactory signals with other nonvolatile ownership signals that are contained in the high molecular weight fraction of male urine. Thus, Gαo impacts on both instinctive and learned social responses to pheromones. CONCLUSIONS: These results highlight that sensory neurons of the Gαo-expressing vomeronasal subsystem, together with the receptors they express and the molecular cues they detect, control a wide range of fundamental mating and reproductive behaviors in female mice. BioMed Central 2014-05-02 /pmc/articles/PMC4038847/ /pubmed/24886577 http://dx.doi.org/10.1186/1741-7007-12-31 Text en Copyright © 2014 Oboti et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Oboti, Livio
Pérez-Gómez, Anabel
Keller, Matthieu
Jacobi, Eric
Birnbaumer, Lutz
Leinders-Zufall, Trese
Zufall, Frank
Chamero, Pablo
A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title_full A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title_fullStr A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title_full_unstemmed A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title_short A wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on G protein Gαo
title_sort wide range of pheromone-stimulated sexual and reproductive behaviors in female mice depend on g protein gαo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038847/
https://www.ncbi.nlm.nih.gov/pubmed/24886577
http://dx.doi.org/10.1186/1741-7007-12-31
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