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P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila
How brains are hardwired to produce aggressive behavior, and how aggression circuits are related to those that mediate courtship, is not well understood. A large-scale screen for aggression-promoting neurons in Drosophila identified several independent hits that enhanced both inter-male aggression a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749567/ https://www.ncbi.nlm.nih.gov/pubmed/26714106 http://dx.doi.org/10.7554/eLife.11346 |
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author | Hoopfer, Eric D Jung, Yonil Inagaki, Hidehiko K Rubin, Gerald M Anderson, David J |
author_facet | Hoopfer, Eric D Jung, Yonil Inagaki, Hidehiko K Rubin, Gerald M Anderson, David J |
author_sort | Hoopfer, Eric D |
collection | PubMed |
description | How brains are hardwired to produce aggressive behavior, and how aggression circuits are related to those that mediate courtship, is not well understood. A large-scale screen for aggression-promoting neurons in Drosophila identified several independent hits that enhanced both inter-male aggression and courtship. Genetic intersections revealed that 8-10 P1 interneurons, previously thought to exclusively control male courtship, were sufficient to promote fighting. Optogenetic experiments indicated that P1 activation could promote aggression at a threshold below that required for wing extension. P1 activation in the absence of wing extension triggered persistent aggression via an internal state that could endure for minutes. High-frequency P1 activation promoted wing extension and suppressed aggression during photostimulation, whereas aggression resumed and wing extension was inhibited following photostimulation offset. Thus, P1 neuron activation promotes a latent, internal state that facilitates aggression and courtship, and controls the overt expression of these social behaviors in a threshold-dependent, inverse manner. DOI: http://dx.doi.org/10.7554/eLife.11346.001 |
format | Online Article Text |
id | pubmed-4749567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47495672016-02-12 P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila Hoopfer, Eric D Jung, Yonil Inagaki, Hidehiko K Rubin, Gerald M Anderson, David J eLife Neuroscience How brains are hardwired to produce aggressive behavior, and how aggression circuits are related to those that mediate courtship, is not well understood. A large-scale screen for aggression-promoting neurons in Drosophila identified several independent hits that enhanced both inter-male aggression and courtship. Genetic intersections revealed that 8-10 P1 interneurons, previously thought to exclusively control male courtship, were sufficient to promote fighting. Optogenetic experiments indicated that P1 activation could promote aggression at a threshold below that required for wing extension. P1 activation in the absence of wing extension triggered persistent aggression via an internal state that could endure for minutes. High-frequency P1 activation promoted wing extension and suppressed aggression during photostimulation, whereas aggression resumed and wing extension was inhibited following photostimulation offset. Thus, P1 neuron activation promotes a latent, internal state that facilitates aggression and courtship, and controls the overt expression of these social behaviors in a threshold-dependent, inverse manner. DOI: http://dx.doi.org/10.7554/eLife.11346.001 eLife Sciences Publications, Ltd 2015-12-29 /pmc/articles/PMC4749567/ /pubmed/26714106 http://dx.doi.org/10.7554/eLife.11346 Text en © 2015, Hoopfer et al 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 Hoopfer, Eric D Jung, Yonil Inagaki, Hidehiko K Rubin, Gerald M Anderson, David J P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title | P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title_full | P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title_fullStr | P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title_full_unstemmed | P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title_short | P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila |
title_sort | p1 interneurons promote a persistent internal state that enhances inter-male aggression in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749567/ https://www.ncbi.nlm.nih.gov/pubmed/26714106 http://dx.doi.org/10.7554/eLife.11346 |
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