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      Salt an Essential Nutrient: Advances in Understanding Salt Taste Detection Using Drosophila as a Model System

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          Abstract

          Taste modalities are conserved in insects and mammals. Sweet gustatory signals evoke attractive behaviors while bitter gustatory information drive aversive behaviors. Salt (NaCl) is an essential nutrient required for various physiological processes, including electrolyte homeostasis, neuronal activity, nutrient absorption, and muscle contraction. Not only mammals, even in Drosophila melanogaster, the detection of NaCl induces two different behaviors: Low concentrations of NaCl act as an attractant, whereas high concentrations act as repellant. The fruit fly is an excellent model system for studying the underlying mechanisms of salt taste due to its relatively simple neuroanatomical organization of the brain and peripheral taste system, the availability of powerful genetic tools and transgenic strains. In this review, we have revisited the literature and the information provided by various laboratories using invertebrate model system Drosophila that has helped us to understand NaCl salt taste so far. We hope that this compiled information from Drosophila will be of general significance and interest for forthcoming studies of the structure, function, and behavioral role of NaCl-sensitive (low and high concentrations) gustatory circuitry for understanding NaCl salt taste in all animals.

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          Mushroom body memoir: from maps to models.

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            The receptors for mammalian sweet and umami taste.

            Sweet and umami (the taste of monosodium glutamate) are the main attractive taste modalities in humans. T1Rs are candidate mammalian taste receptors that combine to assemble two heteromeric G-protein-coupled receptor complexes: T1R1+3, an umami sensor, and T1R2+3, a sweet receptor. We now report the behavioral and physiological characterization of T1R1, T1R2, and T1R3 knockout mice. We demonstrate that sweet and umami taste are strictly dependent on T1R-receptors, and show that selective elimination of T1R-subunits differentially abolishes detection and perception of these two taste modalities. To examine the basis of sweet tastant recognition and coding, we engineered animals expressing either the human T1R2-receptor (hT1R2), or a modified opioid-receptor (RASSL) in sweet cells. Expression of hT1R2 in mice generates animals with humanized sweet taste preferences, while expression of RASSL drives strong attraction to a synthetic opiate, demonstrating that sweet cells trigger dedicated behavioral outputs, but their tastant selectivity is determined by the nature of the receptors.
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              Molecular architecture of smell and taste in Drosophila.

              The chemical senses-smell and taste-allow animals to evaluate and distinguish valuable food resources from dangerous substances in the environment. The central mechanisms by which the brain recognizes and discriminates attractive and repulsive odorants and tastants, and makes behavioral decisions accordingly, are not well understood in any organism. Recent molecular and neuroanatomical advances in Drosophila have produced a nearly complete picture of the peripheral neuroanatomy and function of smell and taste in this insect. Neurophysiological experiments have begun to provide insight into the mechanisms by which these animals process chemosensory cues. Given the considerable anatomical and functional homology in smell and taste pathways in all higher animals, experimental approaches in Drosophila will likely provide broad insights into the problem of sensory coding. Here we provide a critical review of the recent literature in this field and comment on likely future directions.
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                Author and article information

                Journal
                J Exp Neurosci
                J Exp Neurosci
                EXN
                spexn
                Journal of Experimental Neuroscience
                SAGE Publications (Sage UK: London, England )
                1179-0695
                21 November 2018
                2018
                : 12
                : 1179069518806894
                Affiliations
                [1 ]Department of Neurobiology and Genetics, Regional Centre for Biotechnology, NCR Biotech Science Cluster, Faridabad, India
                [2 ]Department of Biotechnology, Maharshi Dayanand University, Rohtak, India
                Author notes
                [*]Pinky Kain, Department of Neurobiology and Genetics, Regional Centre for Biotechnology, NCR Biotech Science Cluster, Faridabad, Haryana - 121001, India. Email: pinkykain@ 123456gmail.com ; pksharma@ 123456rcb.res.in
                Author information
                https://orcid.org/0000-0001-8548-4136
                https://orcid.org/0000-0003-4624-1291
                https://orcid.org/0000-0002-3579-6032
                Article
                10.1177_1179069518806894
                10.1177/1179069518806894
                6249657
                43dc1ff6-749b-468b-bdc5-1f31a157eb16
                © The Author(s) 2018

                This article is distributed under the terms of the Creative Commons Attribution 4.0 License ( http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 10 May 2018
                : 19 September 2018
                Funding
                Funded by: Wellcome trust DBT India Alliance, ;
                Award ID: IA/I/15/2/502074
                Categories
                Review
                Custom metadata
                January-December 2018

                taste,drosophila melanogaster,neural circuits,salt,gustatory neurons,brain

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