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Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses

BACKGROUND: After mating, Drosophila females undergo a remarkable phenotypic switch resulting in decreased sexual receptivity and increased egg laying. Transfer of male sex peptide (SP) during copulation mediates these postmating responses via sensory neurons that coexpress the sex-determination gen...

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Autores principales: Rezával, Carolina, Pavlou, Hania J., Dornan, Anthony J., Chan, Yick-Bun, Kravitz, Edward A., Goodwin, Stephen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396843/
https://www.ncbi.nlm.nih.gov/pubmed/22658598
http://dx.doi.org/10.1016/j.cub.2012.04.062
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author Rezával, Carolina
Pavlou, Hania J.
Dornan, Anthony J.
Chan, Yick-Bun
Kravitz, Edward A.
Goodwin, Stephen F.
author_facet Rezával, Carolina
Pavlou, Hania J.
Dornan, Anthony J.
Chan, Yick-Bun
Kravitz, Edward A.
Goodwin, Stephen F.
author_sort Rezával, Carolina
collection PubMed
description BACKGROUND: After mating, Drosophila females undergo a remarkable phenotypic switch resulting in decreased sexual receptivity and increased egg laying. Transfer of male sex peptide (SP) during copulation mediates these postmating responses via sensory neurons that coexpress the sex-determination gene fruitless (fru) and the proprioceptive neuronal marker pickpocket (ppk) in the female reproductive system. Little is known about the neuronal pathways involved in relaying SP-sensory information to central circuits and how these inputs are processed to direct female-specific changes that occur in response to mating. RESULTS: We demonstrate an essential role played by neurons expressing the sex-determination gene doublesex (dsx) in regulating the female postmating response. We uncovered shared circuitry between dsx and a subset of the previously described SP-responsive fru(+)/ppk(+)-expressing neurons in the reproductive system. In addition, we identified sexually dimorphic dsx circuitry within the abdominal ganglion (Abg) critical for mediating postmating responses. Some of these dsx neurons target posterior regions of the brain while others project onto the uterus. CONCLUSIONS: We propose that dsx-specified circuitry is required to induce female postmating behavioral responses, from sensing SP to conveying this signal to higher-order circuits for processing and through to the generation of postmating behavioral and physiological outputs.
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spelling pubmed-33968432012-07-24 Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses Rezával, Carolina Pavlou, Hania J. Dornan, Anthony J. Chan, Yick-Bun Kravitz, Edward A. Goodwin, Stephen F. Curr Biol Article BACKGROUND: After mating, Drosophila females undergo a remarkable phenotypic switch resulting in decreased sexual receptivity and increased egg laying. Transfer of male sex peptide (SP) during copulation mediates these postmating responses via sensory neurons that coexpress the sex-determination gene fruitless (fru) and the proprioceptive neuronal marker pickpocket (ppk) in the female reproductive system. Little is known about the neuronal pathways involved in relaying SP-sensory information to central circuits and how these inputs are processed to direct female-specific changes that occur in response to mating. RESULTS: We demonstrate an essential role played by neurons expressing the sex-determination gene doublesex (dsx) in regulating the female postmating response. We uncovered shared circuitry between dsx and a subset of the previously described SP-responsive fru(+)/ppk(+)-expressing neurons in the reproductive system. In addition, we identified sexually dimorphic dsx circuitry within the abdominal ganglion (Abg) critical for mediating postmating responses. Some of these dsx neurons target posterior regions of the brain while others project onto the uterus. CONCLUSIONS: We propose that dsx-specified circuitry is required to induce female postmating behavioral responses, from sensing SP to conveying this signal to higher-order circuits for processing and through to the generation of postmating behavioral and physiological outputs. Cell Press 2012-07-10 /pmc/articles/PMC3396843/ /pubmed/22658598 http://dx.doi.org/10.1016/j.cub.2012.04.062 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Rezával, Carolina
Pavlou, Hania J.
Dornan, Anthony J.
Chan, Yick-Bun
Kravitz, Edward A.
Goodwin, Stephen F.
Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title_full Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title_fullStr Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title_full_unstemmed Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title_short Neural Circuitry Underlying Drosophila Female Postmating Behavioral Responses
title_sort neural circuitry underlying drosophila female postmating behavioral responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396843/
https://www.ncbi.nlm.nih.gov/pubmed/22658598
http://dx.doi.org/10.1016/j.cub.2012.04.062
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