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Deep Phenotyping of Sleep in Drosophila
Sleep is an evolutionarily conserved behavior, whose function is unknown. Here, we present a method for deep phenotyping of sleep in Drosophila, consisting of a high-resolution video imaging system, coupled with closed-loop laser perturbation to measure arousal threshold. To quantify sleep-associate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635029/ https://www.ncbi.nlm.nih.gov/pubmed/37961473 http://dx.doi.org/10.1101/2023.10.30.564733 |
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author | Keles, Mehmet F. Sapci, Ali Brody, Casey Palmer, Isabelle Le, Christin Tastan, Oznur Keles, Sunduz Wu, Mark N. |
author_facet | Keles, Mehmet F. Sapci, Ali Brody, Casey Palmer, Isabelle Le, Christin Tastan, Oznur Keles, Sunduz Wu, Mark N. |
author_sort | Keles, Mehmet F. |
collection | PubMed |
description | Sleep is an evolutionarily conserved behavior, whose function is unknown. Here, we present a method for deep phenotyping of sleep in Drosophila, consisting of a high-resolution video imaging system, coupled with closed-loop laser perturbation to measure arousal threshold. To quantify sleep-associated microbehaviors, we trained a deep-learning network to annotate body parts in freely moving flies and developed a semi-supervised computational pipeline to classify behaviors. Quiescent flies exhibit a rich repertoire of microbehaviors, including proboscis pumping (PP) and haltere switches, which vary dynamically across the night. Using this system, we characterized the effects of optogenetically activating two putative sleep circuits. These data reveal that activating dFB neurons produces micromovements, inconsistent with sleep, while activating R5 neurons triggers PP followed by behavioral quiescence. Our findings suggest that sleep in Drosophila is polyphasic with different stages and set the stage for a rigorous analysis of sleep and other behaviors in this species. |
format | Online Article Text |
id | pubmed-10635029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106350292023-11-13 Deep Phenotyping of Sleep in Drosophila Keles, Mehmet F. Sapci, Ali Brody, Casey Palmer, Isabelle Le, Christin Tastan, Oznur Keles, Sunduz Wu, Mark N. bioRxiv Article Sleep is an evolutionarily conserved behavior, whose function is unknown. Here, we present a method for deep phenotyping of sleep in Drosophila, consisting of a high-resolution video imaging system, coupled with closed-loop laser perturbation to measure arousal threshold. To quantify sleep-associated microbehaviors, we trained a deep-learning network to annotate body parts in freely moving flies and developed a semi-supervised computational pipeline to classify behaviors. Quiescent flies exhibit a rich repertoire of microbehaviors, including proboscis pumping (PP) and haltere switches, which vary dynamically across the night. Using this system, we characterized the effects of optogenetically activating two putative sleep circuits. These data reveal that activating dFB neurons produces micromovements, inconsistent with sleep, while activating R5 neurons triggers PP followed by behavioral quiescence. Our findings suggest that sleep in Drosophila is polyphasic with different stages and set the stage for a rigorous analysis of sleep and other behaviors in this species. Cold Spring Harbor Laboratory 2023-11-02 /pmc/articles/PMC10635029/ /pubmed/37961473 http://dx.doi.org/10.1101/2023.10.30.564733 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Keles, Mehmet F. Sapci, Ali Brody, Casey Palmer, Isabelle Le, Christin Tastan, Oznur Keles, Sunduz Wu, Mark N. Deep Phenotyping of Sleep in Drosophila |
title | Deep Phenotyping of Sleep in Drosophila |
title_full | Deep Phenotyping of Sleep in Drosophila |
title_fullStr | Deep Phenotyping of Sleep in Drosophila |
title_full_unstemmed | Deep Phenotyping of Sleep in Drosophila |
title_short | Deep Phenotyping of Sleep in Drosophila |
title_sort | deep phenotyping of sleep in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635029/ https://www.ncbi.nlm.nih.gov/pubmed/37961473 http://dx.doi.org/10.1101/2023.10.30.564733 |
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