@article{307c5d9d2c81485d940199794c4b632f,
title = "Balance of Activity between LNvs and Glutamatergic Dorsal Clock Neurons Promotes Robust Circadian Rhythms in Drosophila",
abstract = "Circadian rhythms offer an excellent opportunity to dissect the neural circuits underlying innate behavior because the genes and neurons involved are relatively well understood. We first sought to understand how Drosophila clock neurons interact in the simple circuit that generates circadian rhythms in larval light avoidance. We used genetics to manipulate two groups of clock neurons, increasing or reducing excitability, stopping their molecular clocks, and blocking neurotransmitter release and reception. Our results revealed that lateral neurons (LNvs) promote and dorsal clock neurons (DN1s) inhibit light avoidance, these neurons probably signal at different times of day, and both signals are required for rhythmic behavior. We found that similar principles apply in the more complex adult circadian circuit that generates locomotor rhythms. Thus, the changing balance in activity between clock neurons with opposing behavioral effects generates robust circadian behavior and probably helps organisms transition between discrete behavioral states, such as sleep and wakefulness.",
author = "Ben Collins and Kane, {Elizabeth A.} and Reeves, {David C.} and Akabas, {Myles H.} and Justin Blau",
note = "Funding Information: We are very grateful to the following for their generous gifts of antibodies and flies: Ravi Allada, Patrick Emery, Paul Hardin, Rob Jackson, Michael Nitabach, Jae Park, Marie-Laure Parmentier, Michael Rosbash, Amita Sehgal, and Mike Young. Additional fly stocks were obtained from the Vienna Drosophila RNAi and Bloomington Stock centers, and PDF antisera were obtained from the DSHB. We also thank Afroditi Petsakou for advice on qPCR and Ravi Allada, Matthieu Cavey, Claude Desplan, Bambos Kyriacou, and Afroditi Petsakou for helpful comments on the manuscript. B.C. was supported by The Robert Leet and Clara Guthrie Patterson Trust Postdoctoral Fellowship, Bank of America, Trustee. E.A.K. was supported by a Dean's Undergraduate Research Fellowship from NYU. This investigation was conducted in a facility constructed with support from Research Facilities Improvement Grant Number C06 RR-15518-01 from the National Center for Research Resources, National Institutes of Health (NIH). Confocal microscopy was performed in the NYU Center for Genomics and Systems Biology Core Facility. This work was supported by NIH grants NS030808 (M.H.A.) and GM063911 (J.B.). ",
year = "2012",
month = may,
day = "24",
doi = "10.1016/j.neuron.2012.02.034",
language = "English (US)",
volume = "74",
pages = "706--718",
journal = "Neuron",
issn = "0896-6273",
publisher = "Cell Press",
number = "4",
}