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Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila
Animals execute one particular behavior among many others in a context-dependent manner, yet the mechanisms underlying such behavioral choice remain poorly understood. Here we studied how two fundamental behaviors, sex and sleep, interact at genetic and neuronal levels in Drosophila. We show that an...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533705/ https://www.ncbi.nlm.nih.gov/pubmed/28754889 http://dx.doi.org/10.1038/s41467-017-00087-5 |
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author | Chen, Dandan Sitaraman, Divya Chen, Nan Jin, Xin Han, Caihong Chen, Jie Sun, Mengshi Baker, Bruce S. Nitabach, Michael N. Pan, Yufeng |
author_facet | Chen, Dandan Sitaraman, Divya Chen, Nan Jin, Xin Han, Caihong Chen, Jie Sun, Mengshi Baker, Bruce S. Nitabach, Michael N. Pan, Yufeng |
author_sort | Chen, Dandan |
collection | PubMed |
description | Animals execute one particular behavior among many others in a context-dependent manner, yet the mechanisms underlying such behavioral choice remain poorly understood. Here we studied how two fundamental behaviors, sex and sleep, interact at genetic and neuronal levels in Drosophila. We show that an increased need for sleep inhibits male sexual behavior by decreasing the activity of the male-specific P1 neurons that coexpress the sex determination genes fru (M) and dsx, but does not affect female sexual behavior. Further, we delineate a sex-specific neuronal circuit wherein the P1 neurons encoding increased courtship drive suppressed male sleep by forming mutually excitatory connections with the fru (M)-positive sleep-controlling DN1 neurons. In addition, we find that FRU(M) regulates male courtship and sleep through distinct neural substrates. These studies reveal the genetic and neuronal basis underlying the sex-specific interaction between sleep and sexual behaviors in Drosophila, and provide insights into how competing behaviors are co-regulated. |
format | Online Article Text |
id | pubmed-5533705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55337052017-08-01 Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila Chen, Dandan Sitaraman, Divya Chen, Nan Jin, Xin Han, Caihong Chen, Jie Sun, Mengshi Baker, Bruce S. Nitabach, Michael N. Pan, Yufeng Nat Commun Article Animals execute one particular behavior among many others in a context-dependent manner, yet the mechanisms underlying such behavioral choice remain poorly understood. Here we studied how two fundamental behaviors, sex and sleep, interact at genetic and neuronal levels in Drosophila. We show that an increased need for sleep inhibits male sexual behavior by decreasing the activity of the male-specific P1 neurons that coexpress the sex determination genes fru (M) and dsx, but does not affect female sexual behavior. Further, we delineate a sex-specific neuronal circuit wherein the P1 neurons encoding increased courtship drive suppressed male sleep by forming mutually excitatory connections with the fru (M)-positive sleep-controlling DN1 neurons. In addition, we find that FRU(M) regulates male courtship and sleep through distinct neural substrates. These studies reveal the genetic and neuronal basis underlying the sex-specific interaction between sleep and sexual behaviors in Drosophila, and provide insights into how competing behaviors are co-regulated. Nature Publishing Group UK 2017-07-28 /pmc/articles/PMC5533705/ /pubmed/28754889 http://dx.doi.org/10.1038/s41467-017-00087-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Dandan Sitaraman, Divya Chen, Nan Jin, Xin Han, Caihong Chen, Jie Sun, Mengshi Baker, Bruce S. Nitabach, Michael N. Pan, Yufeng Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title | Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title_full | Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title_fullStr | Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title_full_unstemmed | Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title_short | Genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in Drosophila |
title_sort | genetic and neuronal mechanisms governing the sex-specific interaction between sleep and sexual behaviors in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533705/ https://www.ncbi.nlm.nih.gov/pubmed/28754889 http://dx.doi.org/10.1038/s41467-017-00087-5 |
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