Modulation of sleep-courtship balance by nutritional status in Drosophila
Sleep is essential but incompatible with other behaviors, and thus sleep drive competes with other motivations. We previously showed Drosophila males balance sleep and courtship via octopaminergic neurons that act upstream of courtship-regulating P1 neurons (Machado et al., 2017). Here, we show nutr...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2020-10-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/60853 |
id |
doaj-b36ab62178724ef28a697a02133ff10f |
---|---|
record_format |
Article |
spelling |
doaj-b36ab62178724ef28a697a02133ff10f2021-05-05T21:37:53ZengeLife Sciences Publications LtdeLife2050-084X2020-10-01910.7554/eLife.60853Modulation of sleep-courtship balance by nutritional status in DrosophilaJosé M Duhart0https://orcid.org/0000-0002-7652-9707Victoria Baccini1Yanan Zhang2Daniel R Machado3Kyunghee Koh4https://orcid.org/0000-0003-0847-8204Department of Neuroscience, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, United StatesDepartment of Neuroscience, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, United StatesDepartment of Neuroscience, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, United StatesDepartment of Neuroscience, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, United States; Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal; ICVS/3B’s, PT Government Associate Laboratory, Braga, PortugalDepartment of Neuroscience, Farber Institute for Neurosciences, Thomas Jefferson University, Philadelphia, United StatesSleep is essential but incompatible with other behaviors, and thus sleep drive competes with other motivations. We previously showed Drosophila males balance sleep and courtship via octopaminergic neurons that act upstream of courtship-regulating P1 neurons (Machado et al., 2017). Here, we show nutrition modulates the sleep-courtship balance and identify sleep-regulatory neurons downstream of P1 neurons. Yeast-deprived males exhibited attenuated female-induced nighttime sleep loss yet normal daytime courtship, which suggests male flies consider nutritional status in deciding whether the potential benefit of pursuing female partners outweighs the cost of losing sleep. Trans-synaptic tracing and calcium imaging identified dopaminergic neurons projecting to the protocerebral bridge (DA-PB) as postsynaptic partners of P1 neurons. Activation of DA-PB neurons led to reduced sleep in normally fed but not yeast-deprived males. Additional PB-projecting neurons regulated male sleep, suggesting several groups of PB-projecting neurons act downstream of P1 neurons to mediate nutritional modulation of the sleep-courtship balance.https://elifesciences.org/articles/60853sleepcourtshipnutritionprotein hungerprotocerebral bridgedecision making |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
José M Duhart Victoria Baccini Yanan Zhang Daniel R Machado Kyunghee Koh |
spellingShingle |
José M Duhart Victoria Baccini Yanan Zhang Daniel R Machado Kyunghee Koh Modulation of sleep-courtship balance by nutritional status in Drosophila eLife sleep courtship nutrition protein hunger protocerebral bridge decision making |
author_facet |
José M Duhart Victoria Baccini Yanan Zhang Daniel R Machado Kyunghee Koh |
author_sort |
José M Duhart |
title |
Modulation of sleep-courtship balance by nutritional status in Drosophila |
title_short |
Modulation of sleep-courtship balance by nutritional status in Drosophila |
title_full |
Modulation of sleep-courtship balance by nutritional status in Drosophila |
title_fullStr |
Modulation of sleep-courtship balance by nutritional status in Drosophila |
title_full_unstemmed |
Modulation of sleep-courtship balance by nutritional status in Drosophila |
title_sort |
modulation of sleep-courtship balance by nutritional status in drosophila |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2020-10-01 |
description |
Sleep is essential but incompatible with other behaviors, and thus sleep drive competes with other motivations. We previously showed Drosophila males balance sleep and courtship via octopaminergic neurons that act upstream of courtship-regulating P1 neurons (Machado et al., 2017). Here, we show nutrition modulates the sleep-courtship balance and identify sleep-regulatory neurons downstream of P1 neurons. Yeast-deprived males exhibited attenuated female-induced nighttime sleep loss yet normal daytime courtship, which suggests male flies consider nutritional status in deciding whether the potential benefit of pursuing female partners outweighs the cost of losing sleep. Trans-synaptic tracing and calcium imaging identified dopaminergic neurons projecting to the protocerebral bridge (DA-PB) as postsynaptic partners of P1 neurons. Activation of DA-PB neurons led to reduced sleep in normally fed but not yeast-deprived males. Additional PB-projecting neurons regulated male sleep, suggesting several groups of PB-projecting neurons act downstream of P1 neurons to mediate nutritional modulation of the sleep-courtship balance. |
topic |
sleep courtship nutrition protein hunger protocerebral bridge decision making |
url |
https://elifesciences.org/articles/60853 |
work_keys_str_mv |
AT josemduhart modulationofsleepcourtshipbalancebynutritionalstatusindrosophila AT victoriabaccini modulationofsleepcourtshipbalancebynutritionalstatusindrosophila AT yananzhang modulationofsleepcourtshipbalancebynutritionalstatusindrosophila AT danielrmachado modulationofsleepcourtshipbalancebynutritionalstatusindrosophila AT kyungheekoh modulationofsleepcourtshipbalancebynutritionalstatusindrosophila |
_version_ |
1721458032929406976 |