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Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila

Circadian rhythms are orchestrated by a master clock that emerges from a network of circadian pacemaker neurons. The master clock is synchronized to external light/dark cycles through photoentrainment, but the circuit mechanisms underlying visual photoentrainment remain largely unknown. Here, we rep...

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Autores principales: Li, Meng-Tong, Cao, Li-Hui, Xiao, Na, Tang, Min, Deng, Bowen, Yang, Tian, Yoshii, Taishi, Luo, Dong-Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185921/
https://www.ncbi.nlm.nih.gov/pubmed/30315165
http://dx.doi.org/10.1038/s41467-018-06506-5
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author Li, Meng-Tong
Cao, Li-Hui
Xiao, Na
Tang, Min
Deng, Bowen
Yang, Tian
Yoshii, Taishi
Luo, Dong-Gen
author_facet Li, Meng-Tong
Cao, Li-Hui
Xiao, Na
Tang, Min
Deng, Bowen
Yang, Tian
Yoshii, Taishi
Luo, Dong-Gen
author_sort Li, Meng-Tong
collection PubMed
description Circadian rhythms are orchestrated by a master clock that emerges from a network of circadian pacemaker neurons. The master clock is synchronized to external light/dark cycles through photoentrainment, but the circuit mechanisms underlying visual photoentrainment remain largely unknown. Here, we report that Drosophila has eye-mediated photoentrainment via a parallel pacemaker neuron organization. Patch-clamp recordings of central circadian pacemaker neurons reveal that light excites most of them independently of one another. We also show that light-responding pacemaker neurons send their dendrites to a neuropil called accessary medulla (aMe), where they make monosynaptic connections with Hofbauer–Buchner eyelet photoreceptors and interneurons that transmit compound-eye signals. Laser ablation of aMe and eye removal both abolish light responses of circadian pacemaker neurons, revealing aMe as a hub to channel eye inputs to central circadian clock. Taken together, we demonstrate that the central clock receives eye inputs via hub-organized parallel circuits in Drosophila.
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spelling pubmed-61859212018-10-15 Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila Li, Meng-Tong Cao, Li-Hui Xiao, Na Tang, Min Deng, Bowen Yang, Tian Yoshii, Taishi Luo, Dong-Gen Nat Commun Article Circadian rhythms are orchestrated by a master clock that emerges from a network of circadian pacemaker neurons. The master clock is synchronized to external light/dark cycles through photoentrainment, but the circuit mechanisms underlying visual photoentrainment remain largely unknown. Here, we report that Drosophila has eye-mediated photoentrainment via a parallel pacemaker neuron organization. Patch-clamp recordings of central circadian pacemaker neurons reveal that light excites most of them independently of one another. We also show that light-responding pacemaker neurons send their dendrites to a neuropil called accessary medulla (aMe), where they make monosynaptic connections with Hofbauer–Buchner eyelet photoreceptors and interneurons that transmit compound-eye signals. Laser ablation of aMe and eye removal both abolish light responses of circadian pacemaker neurons, revealing aMe as a hub to channel eye inputs to central circadian clock. Taken together, we demonstrate that the central clock receives eye inputs via hub-organized parallel circuits in Drosophila. Nature Publishing Group UK 2018-10-12 /pmc/articles/PMC6185921/ /pubmed/30315165 http://dx.doi.org/10.1038/s41467-018-06506-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Meng-Tong
Cao, Li-Hui
Xiao, Na
Tang, Min
Deng, Bowen
Yang, Tian
Yoshii, Taishi
Luo, Dong-Gen
Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title_full Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title_fullStr Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title_full_unstemmed Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title_short Hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in Drosophila
title_sort hub-organized parallel circuits of central circadian pacemaker neurons for visual photoentrainment in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185921/
https://www.ncbi.nlm.nih.gov/pubmed/30315165
http://dx.doi.org/10.1038/s41467-018-06506-5
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