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      Single-cell type analysis of wing premotor circuits in the ventral nerve cord of Drosophila melanogaster

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          Summary

          To perform most behaviors, animals must send commands from higher-order processing centers in the brain to premotor circuits that reside in ganglia distinct from the brain, such as the mammalian spinal cord or insect ventral nerve cord. How these circuits are functionally organized to generate the great diversity of animal behavior remains unclear. An important first step in unraveling the organization of premotor circuits is to identify their constituent cell types and create tools to monitor and manipulate these with high specificity to assess their function. This is possible in the tractable ventral nerve cord of the fly. To generate such a toolkit, we used a combinatorial genetic technique (split-GAL4) to create 195 sparse driver lines targeting 198 individual cell types in the ventral nerve cord. These included wing and haltere motoneurons, modulatory neurons, and interneurons. Using a combination of behavioral, developmental, and anatomical analyses, we systematically characterized the cell types targeted in our collection. Taken together, the resources and results presented here form a powerful toolkit for future investigations of neural circuits and connectivity of premotor circuits while linking them to behavioral outputs.

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          A GAL4-driver line resource for Drosophila neurobiology.

          We established a collection of 7,000 transgenic lines of Drosophila melanogaster. Expression of GAL4 in each line is controlled by a different, defined fragment of genomic DNA that serves as a transcriptional enhancer. We used confocal microscopy of dissected nervous systems to determine the expression patterns driven by each fragment in the adult brain and ventral nerve cord. We present image data on 6,650 lines. Using both manual and machine-assisted annotation, we describe the expression patterns in the most useful lines. We illustrate the utility of these data for identifying novel neuronal cell types, revealing brain asymmetry, and describing the nature and extent of neuronal shape stereotypy. The GAL4 lines allow expression of exogenous genes in distinct, small subsets of the adult nervous system. The set of DNA fragments, each driving a documented expression pattern, will facilitate the generation of additional constructs for manipulating neuronal function. Copyright © 2012 The Authors. Published by Elsevier Inc. All rights reserved.
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            Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects.

            Tetanus toxin cleaves the synaptic vesicle protein synaptobrevin, and the ensuing loss of neurotransmitter exocytosis has implicated synaptobrevin in this process. To further the study of synaptic function in a genetically tractable organism and to generate a tool to disable neuronal communication for behavioural studies, we have expressed a gene encoding tetanus toxin light chain in Drosophila. Toxin expression in embryonic neurons removes detectable synaptobrevin and eliminates evoked, but not spontaneous, synaptic vesicle release. No other developmental or morphological defects are detected. Correspondingly, only synaptobrevin (n-syb), but not the ubiquitously expressed syb protein, is cleaved by tetanus toxin in vitro. Targeted expression of toxin can produce specific behavioral defects; in one case, the olfactory escape response is reduced.
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              The neuronal architecture of the mushroom body provides a logic for associative learning

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                Author and article information

                Journal
                bioRxiv
                BIORXIV
                bioRxiv
                Cold Spring Harbor Laboratory
                01 June 2023
                : 2023.05.31.542897
                Affiliations
                [1 ]Janelia Research Campus, Howard Hughes Medical Institute, 19700 Helix Dr, Ashburn, Virginia 20147, USA
                [2 ]Institute of Zoology, University of Cologne, Zülpicher Str 47b, 50674 Cologne, Germany
                [3 ]Physics Department, Cornell University, 271 Clark Hall, Ithaca, New York 14853, USA
                [4 ]Queensland Brain Institute, University of Queensland, 79 Upland Rd, Brisbane, QLD, 4072, Australia
                [5 ]California Institute of Technology, 1200 E California Blvd, Pasadena, California 91125, USA
                [6 ]Department of Biology, University of Washington, Seattle, Washington 98195, USA
                [7 ]School of Biological Sciences, Faculty of Environmental and Life Sciences, University of Southampton, Life Sciences Building, Southampton SO17 1BJ
                Author notes
                [†]

                These authors contributed equally

                [+]

                present address: Zuckerman Institute, Columbia University. 3227 Broadway, New York, NY 10027, USA

                [* ]Address correspondence to Gwyneth Card, gwyneth.card@ 123456columbia.edu and Wyatt Korff, korffw@ 123456janelia.hhmi.org
                Article
                10.1101/2023.05.31.542897
                10312520
                37398009
                5cdb2440-404d-4aae-a9b0-dd02cad2974f

                This work is licensed under a Creative Commons Attribution 4.0 International License, 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.

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                Article

                drosophila,ventral nerve cord,motoneuron,wing,split-gal4,flight,courtship song

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