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A subclass of evening cells promotes the switch from arousal to sleep at dusk
Animals exhibit rhythmic patterns of behavior that are shaped by an internal circadian clock and the external environment. While light intensity varies across the day, there are particularly robust differences at twilight (dawn/dusk). These periods are also associated with major changes in behaviora...
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/PMC10491161/ https://www.ncbi.nlm.nih.gov/pubmed/37693540 http://dx.doi.org/10.1101/2023.08.28.555147 |
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author | Brown, Matthew P. Verma, Shubha Palmer, Isabelle Zuniga, Adler Guerrero Rosensweig, Clark Keles, Mehmet F. Wu, Mark N. |
author_facet | Brown, Matthew P. Verma, Shubha Palmer, Isabelle Zuniga, Adler Guerrero Rosensweig, Clark Keles, Mehmet F. Wu, Mark N. |
author_sort | Brown, Matthew P. |
collection | PubMed |
description | Animals exhibit rhythmic patterns of behavior that are shaped by an internal circadian clock and the external environment. While light intensity varies across the day, there are particularly robust differences at twilight (dawn/dusk). These periods are also associated with major changes in behavioral states, such as the transition from arousal to sleep. However, the neural mechanisms by which time and environmental conditions promote these behavioral transitions are poorly defined. Here, we show that the E1 subclass of Drosophila evening clock neurons promotes the transition from arousal to sleep at dusk. We first demonstrate that the cell-autonomous clocks of E2 neurons alone are required to drive and adjust the phase of evening anticipation, the canonical behavior associated with “evening” clock neurons. We next show that conditionally silencing E1 neurons causes a significant delay in sleep onset after dusk. However, rather than simply promoting sleep, activating E1 neurons produces time- and light- dependent effects on behavior. Activation of E1 neurons has no effect early in the day, but then triggers arousal before dusk and induces sleep after dusk. Strikingly, these phenotypes critically depend on the presence of light during the day. Despite their influence on behavior around dusk, in vivo voltage imaging of E1 neurons reveals that their spiking rate does not vary between dawn and dusk. Moreover, E1-specific clock ablation has no effect on arousal or sleep. Thus, we suggest that, rather than specifying “evening” time, E1 neurons act, in concert with other rhythmic neurons, to promote behavioral transitions at dusk. |
format | Online Article Text |
id | pubmed-10491161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104911612023-09-09 A subclass of evening cells promotes the switch from arousal to sleep at dusk Brown, Matthew P. Verma, Shubha Palmer, Isabelle Zuniga, Adler Guerrero Rosensweig, Clark Keles, Mehmet F. Wu, Mark N. bioRxiv Article Animals exhibit rhythmic patterns of behavior that are shaped by an internal circadian clock and the external environment. While light intensity varies across the day, there are particularly robust differences at twilight (dawn/dusk). These periods are also associated with major changes in behavioral states, such as the transition from arousal to sleep. However, the neural mechanisms by which time and environmental conditions promote these behavioral transitions are poorly defined. Here, we show that the E1 subclass of Drosophila evening clock neurons promotes the transition from arousal to sleep at dusk. We first demonstrate that the cell-autonomous clocks of E2 neurons alone are required to drive and adjust the phase of evening anticipation, the canonical behavior associated with “evening” clock neurons. We next show that conditionally silencing E1 neurons causes a significant delay in sleep onset after dusk. However, rather than simply promoting sleep, activating E1 neurons produces time- and light- dependent effects on behavior. Activation of E1 neurons has no effect early in the day, but then triggers arousal before dusk and induces sleep after dusk. Strikingly, these phenotypes critically depend on the presence of light during the day. Despite their influence on behavior around dusk, in vivo voltage imaging of E1 neurons reveals that their spiking rate does not vary between dawn and dusk. Moreover, E1-specific clock ablation has no effect on arousal or sleep. Thus, we suggest that, rather than specifying “evening” time, E1 neurons act, in concert with other rhythmic neurons, to promote behavioral transitions at dusk. Cold Spring Harbor Laboratory 2023-08-29 /pmc/articles/PMC10491161/ /pubmed/37693540 http://dx.doi.org/10.1101/2023.08.28.555147 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Brown, Matthew P. Verma, Shubha Palmer, Isabelle Zuniga, Adler Guerrero Rosensweig, Clark Keles, Mehmet F. Wu, Mark N. A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title | A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title_full | A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title_fullStr | A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title_full_unstemmed | A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title_short | A subclass of evening cells promotes the switch from arousal to sleep at dusk |
title_sort | subclass of evening cells promotes the switch from arousal to sleep at dusk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491161/ https://www.ncbi.nlm.nih.gov/pubmed/37693540 http://dx.doi.org/10.1101/2023.08.28.555147 |
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