Abstract

The circadian system produces ~24-hr oscillations in behavioral and physiological processes to ensure that they occur at optimal times of day and in the correct temporal order. At its core, the circadian system is composed of dedicated central clock neurons that keep time through a cell-autonomous molecular clock. To produce rhythmic behaviors, time-of-day information generated by clock neurons must be transmitted across output pathways to regulate the downstream neuronal populations that control the relevant behaviors. An understanding of the manner through which the circadian system enacts behavioral rhythms therefore requires the identification of the cells and molecules that make up the output pathways. To that end, we recently characterized the Drosophila pars intercerebralis (PI) as a major circadian output center that lies downstream of central clock neurons in a circuit controlling rest:activity rhythms. We have conducted single-cell RNA sequencing (scRNAseq) to identify potential circadian output genes expressed by PI cells, and used cell-specific RNA interference (RNAi) to knock down expression of ~40 of these candidate genes selectively within subsets of PI cells. We demonstrate that knockdown of the slowpoke (slo) potassium channel in PI cells reliably decreases circadian rest:activity rhythm strength. Interestingly, slo mutants have previously been shown to have aberrant rest:activity rhythms, in part due to a necessary function of slo within central clock cells. However, rescue of slo in all clock cells does not fully reestablish behavioral rhythms, indicating that expression in non-clock neurons is also necessary. Our results demonstrate that slo exerts its effects in multiple components of the circadian circuit, including PI output cells in addition to clock neurons, and we hypothesize that it does so by contributing to the generation of daily neuronal activity rhythms that allow for the propagation of circadian information throughout output circuits.

Highlights

  • Behavioral circadian rhythms depend on dedicated clock neurons in the brain that track time of day through the function of a molecular circadian clock

  • pars intercerebralis (PI) cell expression of receptors for neuropeptides and small molecular neurotransmitters implicated in circadian rhythm regulation

  • We previously demonstrated that non-Drosophila insulin-like peptides (DILPs)-expressing PI cells comprise essential components of a circadian output circuit controlling rest:activity rhythms [4, 5]

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Summary

Introduction

Behavioral circadian rhythms depend on dedicated clock neurons in the brain that track time of day through the function of a molecular circadian clock. Drosophila melanogaster, there are ~150 central clock neurons in the brain, as determined by expression of components of the molecular clock. These clock neurons include the large and small ventral lateral. Slowpoke regulates circadian outputs www.nigms.nih.gov/, Grant R15GM128170 to D.J. C, and the Brain and Behavior Research Foundation, https://www.bbrfoundation.org/, Young Investigator Grant #24045 to D.J.C. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

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