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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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.
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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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