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Drosulfakinin signaling modulates female sexual receptivity in Drosophila
Female sexual behavior as an innate behavior is of prominent biological importance for survival and reproduction. However, molecular and circuit mechanisms underlying female sexual behavior is not well understood. Here, we identify the Cholecystokinin-like peptide Drosulfakinin (DSK) to promote fema...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045819/ https://www.ncbi.nlm.nih.gov/pubmed/35475782 http://dx.doi.org/10.7554/eLife.76025 |
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author | Wang, Tao Jing, Biyang Deng, Bowen Shi, Kai Li, Jing Ma, Baoxu Wu, Fengming Zhou, Chuan |
author_facet | Wang, Tao Jing, Biyang Deng, Bowen Shi, Kai Li, Jing Ma, Baoxu Wu, Fengming Zhou, Chuan |
author_sort | Wang, Tao |
collection | PubMed |
description | Female sexual behavior as an innate behavior is of prominent biological importance for survival and reproduction. However, molecular and circuit mechanisms underlying female sexual behavior is not well understood. Here, we identify the Cholecystokinin-like peptide Drosulfakinin (DSK) to promote female sexual behavior in Drosophila. Loss of DSK function reduces female receptivity while overexpressing DSK enhances female receptivity. We identify two pairs of Dsk-expressing neurons in the central brain to promote female receptivity. We find that the DSK peptide acts through one of its receptors, CCKLR-17D3, to modulate female receptivity. Manipulation of CCKLR-17D3 and its expressing neurons alters female receptivity. We further reveal that the two pairs of Dsk-expressing neurons receive input signal from pC1 neurons that integrate sex-related cues and mating status. These results demonstrate how a neuropeptide pathway interacts with a central neural node in the female sex circuitry to modulate sexual receptivity. |
format | Online Article Text |
id | pubmed-9045819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-90458192022-04-28 Drosulfakinin signaling modulates female sexual receptivity in Drosophila Wang, Tao Jing, Biyang Deng, Bowen Shi, Kai Li, Jing Ma, Baoxu Wu, Fengming Zhou, Chuan eLife Neuroscience Female sexual behavior as an innate behavior is of prominent biological importance for survival and reproduction. However, molecular and circuit mechanisms underlying female sexual behavior is not well understood. Here, we identify the Cholecystokinin-like peptide Drosulfakinin (DSK) to promote female sexual behavior in Drosophila. Loss of DSK function reduces female receptivity while overexpressing DSK enhances female receptivity. We identify two pairs of Dsk-expressing neurons in the central brain to promote female receptivity. We find that the DSK peptide acts through one of its receptors, CCKLR-17D3, to modulate female receptivity. Manipulation of CCKLR-17D3 and its expressing neurons alters female receptivity. We further reveal that the two pairs of Dsk-expressing neurons receive input signal from pC1 neurons that integrate sex-related cues and mating status. These results demonstrate how a neuropeptide pathway interacts with a central neural node in the female sex circuitry to modulate sexual receptivity. eLife Sciences Publications, Ltd 2022-04-27 /pmc/articles/PMC9045819/ /pubmed/35475782 http://dx.doi.org/10.7554/eLife.76025 Text en © 2022, Wang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Wang, Tao Jing, Biyang Deng, Bowen Shi, Kai Li, Jing Ma, Baoxu Wu, Fengming Zhou, Chuan Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title | Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title_full | Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title_fullStr | Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title_full_unstemmed | Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title_short | Drosulfakinin signaling modulates female sexual receptivity in Drosophila |
title_sort | drosulfakinin signaling modulates female sexual receptivity in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9045819/ https://www.ncbi.nlm.nih.gov/pubmed/35475782 http://dx.doi.org/10.7554/eLife.76025 |
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