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Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila
Sleep is a highly conserved and essential behaviour in many species, including the fruit fly Drosophila melanogaster. In the wild, sensory signalling encoding environmental information must be integrated with sleep drive to ensure that sleep is not initiated during detrimental conditions. However, t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5233985/ https://www.ncbi.nlm.nih.gov/pubmed/28084307 http://dx.doi.org/10.1038/srep40304 |
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author | Lamaze, Angelique Öztürk-Çolak, Arzu Fischer, Robin Peschel, Nicolai Koh, Kyunghee Jepson, James E. C. |
author_facet | Lamaze, Angelique Öztürk-Çolak, Arzu Fischer, Robin Peschel, Nicolai Koh, Kyunghee Jepson, James E. C. |
author_sort | Lamaze, Angelique |
collection | PubMed |
description | Sleep is a highly conserved and essential behaviour in many species, including the fruit fly Drosophila melanogaster. In the wild, sensory signalling encoding environmental information must be integrated with sleep drive to ensure that sleep is not initiated during detrimental conditions. However, the molecular and circuit mechanisms by which sleep timing is modulated by the environment are unclear. Here we introduce a novel behavioural paradigm to study this issue. We show that in male fruit flies, onset of the daytime siesta is delayed by ambient temperatures above 29 °C. We term this effect Prolonged Morning Wakefulness (PMW). We show that signalling through the TrpA1 thermo-sensor is required for PMW, and that TrpA1 specifically impacts siesta onset, but not night sleep onset, in response to elevated temperatures. We identify two critical TrpA1-expressing circuits and show that both contact DN1p clock neurons, the output of which is also required for PMW. Finally, we identify the circadian blue-light photoreceptor CRYPTOCHROME as a molecular regulator of PMW, and propose a model in which the Drosophila nervous system integrates information encoding temperature, light, and time to dynamically control when sleep is initiated. Our results provide a platform to investigate how environmental inputs co-ordinately regulate sleep plasticity. |
format | Online Article Text |
id | pubmed-5233985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52339852017-01-17 Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila Lamaze, Angelique Öztürk-Çolak, Arzu Fischer, Robin Peschel, Nicolai Koh, Kyunghee Jepson, James E. C. Sci Rep Article Sleep is a highly conserved and essential behaviour in many species, including the fruit fly Drosophila melanogaster. In the wild, sensory signalling encoding environmental information must be integrated with sleep drive to ensure that sleep is not initiated during detrimental conditions. However, the molecular and circuit mechanisms by which sleep timing is modulated by the environment are unclear. Here we introduce a novel behavioural paradigm to study this issue. We show that in male fruit flies, onset of the daytime siesta is delayed by ambient temperatures above 29 °C. We term this effect Prolonged Morning Wakefulness (PMW). We show that signalling through the TrpA1 thermo-sensor is required for PMW, and that TrpA1 specifically impacts siesta onset, but not night sleep onset, in response to elevated temperatures. We identify two critical TrpA1-expressing circuits and show that both contact DN1p clock neurons, the output of which is also required for PMW. Finally, we identify the circadian blue-light photoreceptor CRYPTOCHROME as a molecular regulator of PMW, and propose a model in which the Drosophila nervous system integrates information encoding temperature, light, and time to dynamically control when sleep is initiated. Our results provide a platform to investigate how environmental inputs co-ordinately regulate sleep plasticity. Nature Publishing Group 2017-01-13 /pmc/articles/PMC5233985/ /pubmed/28084307 http://dx.doi.org/10.1038/srep40304 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lamaze, Angelique Öztürk-Çolak, Arzu Fischer, Robin Peschel, Nicolai Koh, Kyunghee Jepson, James E. C. Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title | Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title_full | Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title_fullStr | Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title_full_unstemmed | Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title_short | Regulation of sleep plasticity by a thermo-sensitive circuit in Drosophila |
title_sort | regulation of sleep plasticity by a thermo-sensitive circuit in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5233985/ https://www.ncbi.nlm.nih.gov/pubmed/28084307 http://dx.doi.org/10.1038/srep40304 |
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