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Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development
Sleep and feeding patterns lack a clear daily rhythm during early life. As diurnal animals mature, feeding is consolidated to the day and sleep to the night. Circadian sleep patterns begin with formation of a circuit connecting the central clock to arousal output neurons; emergence of circadian slee...
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/PMC10541615/ https://www.ncbi.nlm.nih.gov/pubmed/37786713 http://dx.doi.org/10.1101/2023.09.19.558472 |
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author | Poe, Amy R. Zhu, Lucy Tang, Si Hao Valencia, Ella Kayser, Matthew S. |
author_facet | Poe, Amy R. Zhu, Lucy Tang, Si Hao Valencia, Ella Kayser, Matthew S. |
author_sort | Poe, Amy R. |
collection | PubMed |
description | Sleep and feeding patterns lack a clear daily rhythm during early life. As diurnal animals mature, feeding is consolidated to the day and sleep to the night. Circadian sleep patterns begin with formation of a circuit connecting the central clock to arousal output neurons; emergence of circadian sleep also enables long-term memory (LTM). However, the cues that trigger the development of this clock-arousal circuit are unknown. Here, we identify a role for nutritional status in driving sleep-wake rhythm development in Drosophila larvae. We find that in the 2(nd) instar (L2) period, sleep and feeding are spread across the day; these behaviors become organized into daily patterns by L3. Forcing mature (L3) animals to adopt immature (L2) feeding strategies disrupts sleep-wake rhythms and the ability to exhibit LTM. In addition, the development of the clock (DN1a)-arousal (Dh44) circuit itself is influenced by the larval nutritional environment. Finally, we demonstrate that larval arousal Dh44 neurons act through glucose metabolic genes to drive onset of daily sleep-wake rhythms. Together, our data suggest that changes to energetic demands in developing organisms triggers the formation of sleep-circadian circuits and behaviors. |
format | Online Article Text |
id | pubmed-10541615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105416152023-10-02 Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development Poe, Amy R. Zhu, Lucy Tang, Si Hao Valencia, Ella Kayser, Matthew S. bioRxiv Article Sleep and feeding patterns lack a clear daily rhythm during early life. As diurnal animals mature, feeding is consolidated to the day and sleep to the night. Circadian sleep patterns begin with formation of a circuit connecting the central clock to arousal output neurons; emergence of circadian sleep also enables long-term memory (LTM). However, the cues that trigger the development of this clock-arousal circuit are unknown. Here, we identify a role for nutritional status in driving sleep-wake rhythm development in Drosophila larvae. We find that in the 2(nd) instar (L2) period, sleep and feeding are spread across the day; these behaviors become organized into daily patterns by L3. Forcing mature (L3) animals to adopt immature (L2) feeding strategies disrupts sleep-wake rhythms and the ability to exhibit LTM. In addition, the development of the clock (DN1a)-arousal (Dh44) circuit itself is influenced by the larval nutritional environment. Finally, we demonstrate that larval arousal Dh44 neurons act through glucose metabolic genes to drive onset of daily sleep-wake rhythms. Together, our data suggest that changes to energetic demands in developing organisms triggers the formation of sleep-circadian circuits and behaviors. Cold Spring Harbor Laboratory 2023-09-22 /pmc/articles/PMC10541615/ /pubmed/37786713 http://dx.doi.org/10.1101/2023.09.19.558472 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Poe, Amy R. Zhu, Lucy Tang, Si Hao Valencia, Ella Kayser, Matthew S. Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title | Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title_full | Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title_fullStr | Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title_full_unstemmed | Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title_short | Energetic Demands Regulate Sleep-Wake Rhythm Circuit Development |
title_sort | energetic demands regulate sleep-wake rhythm circuit development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541615/ https://www.ncbi.nlm.nih.gov/pubmed/37786713 http://dx.doi.org/10.1101/2023.09.19.558472 |
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