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Here, we describe the embryonic central nervous system expression of 5,000 GAL4 lines made using molecularly defined cis-regulatory DNA inserted into a single attP genomic location. We document and annotate the patterns in early embryos when neurogenesis is at its peak, and in older embryos where there is maximal neuronal diversity and the first neural circuits are established. We note expression in other tissues, such as the lateral body wall (muscle, sensory neurons, and trachea) and viscera. Companion papers report on the adult brain and larval imaginal discs, and the integrated data sets are available online (http://www.janelia.org/gal4-gen1). This collection of embryonically expressed GAL4 lines will be valuable for determining neuronal morphology and function. The 1,862 lines expressed in small subsets of neurons (<20/segment) will be especially valuable for characterizing interneuronal diversity and function, because although interneurons comprise the majority of all central nervous system neurons, their gene expression profile and function remain virtually unexplored.
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http://dx.doi.org/10.1016/j.celrep.2012.09.009 | DOI Listing |
Biomed J
August 2025
Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Department of Biochemistry, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Department of Neurology, New Taipei Municipal TuCheng Hospital, Chang Gung Memorial Hospital, New Taipei Ci
Background: Thirst and hunger are fundamental survival drives that modulate various aspects of animal behavior through specific neural circuits. Previous studies have demonstrated that dopaminergic neurons (DANs) innervating the mushroom body (MB) in the Drosophila brain play essential roles in innate and learned thirst- and hunger-dependent behaviors, with most experiments focusing on acute water or food deprivation. However, it is unclear whether acute water or food deprivation alters dopamine production and neural activity in MB-innervating DANs.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Entomology, Cornell University, Ithaca, NY, United States of America.
The ability to direct tissue-specific overexpression of transgenic proteins in genetically tractable organisms like has facilitated innumerable biological discoveries. However, transgenic proteins can themselves impact cellular and physiological processes in ways that are often ignored or poorly defined. Here we discovered that the transgene, which directs strong expression of the yeast GAL4 transcription factor in the fat body, induces significant physiological defects in adult female flies.
View Article and Find Full Text PDFDis Model Mech
July 2025
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Peroxisomal biogenesis disorders (PBD) are autosomal recessive diseases caused by mutations in specific PEX genes that impair peroxisome formation, leading to multi-systemic failure. Symptoms vary, even in patients with variants in the same PEX gene. Our goal is to select PEX mutations and use Drosophila to model a severity spectrum based on genotype-phenotype correlations.
View Article and Find Full Text PDFbioRxiv
May 2025
Princeton Neuroscience Institute, Princeton University, Princeton, NJ USA.
Nervous systems rely on sensory feature maps, where the tuning of neighboring neurons for some ethologically-relevant parameter varies systematically, to control behavior. Such maps can be organized topographically or based on some computational principle. However, it is unclear how the central organization of a sensory system corresponds to the functional logic of the motor system.
View Article and Find Full Text PDFElife
June 2025
School of Science and Engineering, Division Biological and Biomedical Systems, University of Missouri-Kansas City, Kansas City, United States.
Understanding developmental changes in neuronal lineages is crucial to elucidate how they assemble into functional neural networks. Studies investigating nervous system development in model systems have only focused on select regions of the CNS due to the limited availability of genetic drivers that target specific neuronal lineages throughout development and adult life. This has hindered our understanding of how distinct neuronal lineages interconnect to form neuronal circuits during development.
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