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Cell types and neuronal circuitry underlying female aggression in Drosophila
Aggressive social interactions are used to compete for limited resources and are regulated by complex sensory cues and the organism’s internal state. While both sexes exhibit aggression, its neuronal underpinnings are understudied in females. Here, we identify a population of sexually dimorphic aIPg...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787668/ https://www.ncbi.nlm.nih.gov/pubmed/33141021 http://dx.doi.org/10.7554/eLife.58942 |
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author | Schretter, Catherine E Aso, Yoshinori Robie, Alice A Dreher, Marisa Dolan, Michael-John Chen, Nan Ito, Masayoshi Yang, Tansy Parekh, Ruchi Branson, Kristin M Rubin, Gerald M |
author_facet | Schretter, Catherine E Aso, Yoshinori Robie, Alice A Dreher, Marisa Dolan, Michael-John Chen, Nan Ito, Masayoshi Yang, Tansy Parekh, Ruchi Branson, Kristin M Rubin, Gerald M |
author_sort | Schretter, Catherine E |
collection | PubMed |
description | Aggressive social interactions are used to compete for limited resources and are regulated by complex sensory cues and the organism’s internal state. While both sexes exhibit aggression, its neuronal underpinnings are understudied in females. Here, we identify a population of sexually dimorphic aIPg neurons in the adult Drosophila melanogaster central brain whose optogenetic activation increased, and genetic inactivation reduced, female aggression. Analysis of GAL4 lines identified in an unbiased screen for increased female chasing behavior revealed the involvement of another sexually dimorphic neuron, pC1d, and implicated aIPg and pC1d neurons as core nodes regulating female aggression. Connectomic analysis demonstrated that aIPg neurons and pC1d are interconnected and suggest that aIPg neurons may exert part of their effect by gating the flow of visual information to descending neurons. Our work reveals important regulatory components of the neuronal circuitry that underlies female aggressive social interactions and provides tools for their manipulation. |
format | Online Article Text |
id | pubmed-7787668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-77876682021-01-11 Cell types and neuronal circuitry underlying female aggression in Drosophila Schretter, Catherine E Aso, Yoshinori Robie, Alice A Dreher, Marisa Dolan, Michael-John Chen, Nan Ito, Masayoshi Yang, Tansy Parekh, Ruchi Branson, Kristin M Rubin, Gerald M eLife Neuroscience Aggressive social interactions are used to compete for limited resources and are regulated by complex sensory cues and the organism’s internal state. While both sexes exhibit aggression, its neuronal underpinnings are understudied in females. Here, we identify a population of sexually dimorphic aIPg neurons in the adult Drosophila melanogaster central brain whose optogenetic activation increased, and genetic inactivation reduced, female aggression. Analysis of GAL4 lines identified in an unbiased screen for increased female chasing behavior revealed the involvement of another sexually dimorphic neuron, pC1d, and implicated aIPg and pC1d neurons as core nodes regulating female aggression. Connectomic analysis demonstrated that aIPg neurons and pC1d are interconnected and suggest that aIPg neurons may exert part of their effect by gating the flow of visual information to descending neurons. Our work reveals important regulatory components of the neuronal circuitry that underlies female aggressive social interactions and provides tools for their manipulation. eLife Sciences Publications, Ltd 2020-11-03 /pmc/articles/PMC7787668/ /pubmed/33141021 http://dx.doi.org/10.7554/eLife.58942 Text en © 2020, Schretter et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Schretter, Catherine E Aso, Yoshinori Robie, Alice A Dreher, Marisa Dolan, Michael-John Chen, Nan Ito, Masayoshi Yang, Tansy Parekh, Ruchi Branson, Kristin M Rubin, Gerald M Cell types and neuronal circuitry underlying female aggression in Drosophila |
title | Cell types and neuronal circuitry underlying female aggression in Drosophila |
title_full | Cell types and neuronal circuitry underlying female aggression in Drosophila |
title_fullStr | Cell types and neuronal circuitry underlying female aggression in Drosophila |
title_full_unstemmed | Cell types and neuronal circuitry underlying female aggression in Drosophila |
title_short | Cell types and neuronal circuitry underlying female aggression in Drosophila |
title_sort | cell types and neuronal circuitry underlying female aggression in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787668/ https://www.ncbi.nlm.nih.gov/pubmed/33141021 http://dx.doi.org/10.7554/eLife.58942 |
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