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A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior
Although males and females largely share the same genome and nervous system, they differ profoundly in reproductive investments and require distinct behavioral, morphological, and physiological adaptations. How can the nervous system, while bound by both developmental and biophysical constraints, pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987718/ https://www.ncbi.nlm.nih.gov/pubmed/33508219 http://dx.doi.org/10.1016/j.cub.2020.12.047 |
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author | Nojima, Tetsuya Rings, Annika Allen, Aaron M. Otto, Nils Verschut, Thomas A. Billeter, Jean-Christophe Neville, Megan C. Goodwin, Stephen F. |
author_facet | Nojima, Tetsuya Rings, Annika Allen, Aaron M. Otto, Nils Verschut, Thomas A. Billeter, Jean-Christophe Neville, Megan C. Goodwin, Stephen F. |
author_sort | Nojima, Tetsuya |
collection | PubMed |
description | Although males and females largely share the same genome and nervous system, they differ profoundly in reproductive investments and require distinct behavioral, morphological, and physiological adaptations. How can the nervous system, while bound by both developmental and biophysical constraints, produce these sex differences in behavior? Here, we uncover a novel dimorphism in Drosophila melanogaster that allows deployment of completely different behavioral repertoires in males and females with minimum changes to circuit architecture. Sexual differentiation of only a small number of higher order neurons in the brain leads to a change in connectivity related to the primary reproductive needs of both sexes—courtship pursuit in males and communal oviposition in females. This study explains how an apparently similar brain generates distinct behavioral repertoires in the two sexes and presents a fundamental principle of neural circuit organization that may be extended to other species. |
format | Online Article Text |
id | pubmed-7987718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79877182021-03-24 A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior Nojima, Tetsuya Rings, Annika Allen, Aaron M. Otto, Nils Verschut, Thomas A. Billeter, Jean-Christophe Neville, Megan C. Goodwin, Stephen F. Curr Biol Article Although males and females largely share the same genome and nervous system, they differ profoundly in reproductive investments and require distinct behavioral, morphological, and physiological adaptations. How can the nervous system, while bound by both developmental and biophysical constraints, produce these sex differences in behavior? Here, we uncover a novel dimorphism in Drosophila melanogaster that allows deployment of completely different behavioral repertoires in males and females with minimum changes to circuit architecture. Sexual differentiation of only a small number of higher order neurons in the brain leads to a change in connectivity related to the primary reproductive needs of both sexes—courtship pursuit in males and communal oviposition in females. This study explains how an apparently similar brain generates distinct behavioral repertoires in the two sexes and presents a fundamental principle of neural circuit organization that may be extended to other species. Cell Press 2021-03-22 /pmc/articles/PMC7987718/ /pubmed/33508219 http://dx.doi.org/10.1016/j.cub.2020.12.047 Text en © 2021 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nojima, Tetsuya Rings, Annika Allen, Aaron M. Otto, Nils Verschut, Thomas A. Billeter, Jean-Christophe Neville, Megan C. Goodwin, Stephen F. A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title | A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title_full | A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title_fullStr | A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title_full_unstemmed | A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title_short | A sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
title_sort | sex-specific switch between visual and olfactory inputs underlies adaptive sex differences in behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987718/ https://www.ncbi.nlm.nih.gov/pubmed/33508219 http://dx.doi.org/10.1016/j.cub.2020.12.047 |
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