cAMP response element-binding protein (CREB) and nuclear factor kappa-B (NF-κB) are two ubiquitous transcription factors involved in a wide number of cellular processes, including the circadian system. Many previous studies on these factors use cellular assays that provide limited information on circadian activity or anatomical specificity. The ability to study transcription factors in defined tissue within intact animals will help to bridge the gap between cellular and in vivo data. We have used the GAL4-UAS and FLP-FRT systems to gain spatial control over reporter gene expression. Using a luciferase-based reporter, we show in vivo that Drosophila dCREB2- and NF-κB-mediated transcription oscillates in neuronal cells, glia, and in the mushroom body, a higher-order brain center in flies. This oscillation is under circadian control, cycling with a 24-hour rhythm, under both light-dark and dark-dark conditions. In light-light conditions, dCREB2 and NF-κB reporter flies exhibit a suppression of rhythmic activity. Furthermore, neuronal cycling of dCREB2 and NF-κB activity are modulated in period mutant flies, indicating these oscillations are controlled through the central clock. This study shows for the first time region-specific circadian oscillation of dCREB2/NF-κB activity in the Drosophila nervous system.
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Curr Biol
June 2019
Institut für Entwicklungsbiologie und Neurobiologie, Johannes Gutenberg-Universität Mainz, Hanns-Dieter-Hüsch-Weg 15, 55099 Mainz, Germany. Electronic address:
Grasping an object or crossing a trench requires the integration of information on the operating distance of our limbs with precise distance estimation. The reach of our hands and step size of our legs are learned by the visual feedback we get during our actions. This implicit knowledge of our peripersonal space is first acquired during infancy but will be continuously updated throughout our whole life [1].
View Article and Find Full Text PDFHum Mol Genet
March 2016
Department of Medical Genetics, Department of Neurology, University of Wisconsin-Madison, 1685 Highland Ave., Madison, WI 53705-2281, USA
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View Article and Find Full Text PDFNeurobiol Learn Mem
February 2015
Department of Genetics, 3434 Genetics/Biotechnology, 425 Henry Mall, University of Wisconsin-Madison, Madison, WI 53706, United States; Department of Neurology, 1685 Highland Ave., University of Wisconsin-Madison, Madison, WI 53706, United States. Electronic address:
CREB (cAMP response element-binding protein) is an evolutionarily conserved transcription factor, playing key roles in synaptic plasticity, intrinsic excitability and long-term memory (LTM) formation. The Drosophila homologue of mammalian CREB, dCREB2, is also important for LTM. However, the spatio-temporal nature of dCREB2 activity during memory consolidation is poorly understood.
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April 2014
Departments of Genetics, University of Wisconsin-Madison Madison, WI, USA ; Department of Neurology, University of Wisconsin-Madison Madison, WI, USA.
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View Article and Find Full Text PDFNeurobiol Learn Mem
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Neuroscience Training Program, University of Wisconsin-Madison, 1300 University Ave., Madison, WI 53706, United States; Department of Genetics, University of Wisconsin-Madison, 3434 Genetics/Biotechnology, 425 Henry Mall, Madison, WI 53706, United States. Electronic address:
The transcription factor CREB is an important regulator of many adaptive processes in neurons, including sleep, cellular homeostasis, and memory formation. The Drosophila dCREB2 family includes multiple protein isoforms generated from a single gene. Overexpression of an activator or blocker isoform has been shown to enhance or block memory formation, but the molecular mechanisms underlying these phenomena remain unclear.
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