45
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      The chemical component of the mixed GF-TTMn synapse in Drosophila melanogaster uses acetylcholine as its neurotransmitter

      brief-report

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The largest central synapse in adult Drosophila is a mixed electro-chemical synapse whose gap junctions require the product of the shaking-B (shak-B) gene. Shak-B 2 mutant flies lack gap junctions at this synapse, which is between the giant fibre (GF) and the tergotrochanteral motor neuron (TTMn), but it still exhibits a long latency response upon GF stimulation. We have targeted the expression of the light chain of tetanus toxin to the GF, to block chemical transmission, in shak-B 2 flies. The long latency response in the tergotrochanteral muscle (TTM) was abolished indicating that the chemical component of the synapse mediates this response. Attenuation of GAL4-mediated labelling by a cha-GAL80 transgene, reveals the GF to be cholinergic. We have used a temperature-sensitive allele of the choline acetyltransferase gene ( cha ts2) to block cholinergic synapses in adult flies and this also abolished the long latency response in shak-B 2 flies. Taken together the data provide evidence that both components of this mixed synapse are functional and that the chemical neurotransmitter between the GF and the TTMn is acetylcholine. Our findings show that the two components of this synapse can be separated to allow further studies into the mechanisms by which mixed synapses are built and function.

          Related collections

          Most cited references37

          • Record: found
          • Abstract: found
          • Article: not found

          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.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The Mauthner cell half a century later: a neurobiological model for decision-making?

            The Mauthner (M) cell is a critical element in a vital escape "reflex" triggered by abrupt or threatening events. Its properties at the molecular and synaptic levels, their various forms of plasticity, and the design of its networks, are all well adapted for this survival function. They guarantee that this behavior is appropriately unilateral, variable, and unpredictable. The M cell sets the behavioral threshold, and, acting in concert with other elements of the brainstem escape network, determines when, where, and how the escape is executed.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Fifty years of a command neuron: the neurobiology of escape behavior in the crayfish.

              Fifty years ago C.A.G. Wiersma established that the giant axons of the crayfish nerve cord drive tail-flip escape responses. The circuitry that includes these giant neurons has now become one of the best-understood neural circuits in the animal kingdom. Although it controls a specialized behavior of a relatively simple animal, this circuitry has provided insights that are of general neurobiological interest concerning matters as diverse as the identity of the neural substrates involved in making behavioral decisions, the cellular bases of learning, subcellular neuronal computation, voltage-gated electrical synaptic transmission and modification of neuromodulator actions that result from social experience. This work illustrates the value of studying a circuit of moderate, but tractable, complexity and known behavioral function.
                Bookmark

                Author and article information

                Journal
                Eur J Neurosci
                ejn
                The European Journal of Neuroscience
                Blackwell Publishing Ltd
                0953-816X
                1460-9568
                01 July 2007
                : 26
                : 2
                : 439-445
                Affiliations
                [1 ]Department of Biosciences, University of Kent, Canterbury Kent, CT2 7NJ, UK
                [2 ]Department of Biology, Morrill Science Center, University of Massachusetts, Amherst Massachusetts 01003, USA
                Author notes
                Dr Marcus J. Allen, as above. E-mail: M.J.Allen@ 123456kent.ac.uk
                [*]

                Present address: Department of Biological Sciences, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431, USA.

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                Article
                10.1111/j.1460-9568.2007.05686.x
                1974813
                17650116
                798d21aa-30ce-420d-87ab-fa25765e6a5c
                © The Authors (2007). Journal Compilation © Federation of European Neuroscience Societies and Blackwell Publishing Ltd
                History
                : 18 April 2007
                : 05 June 2007
                : 06 June 2007
                Categories
                Research Reports

                Neurosciences
                giant fibre,neuron,neurotransmitter,innexins,tetanus toxin
                Neurosciences
                giant fibre, neuron, neurotransmitter, innexins, tetanus toxin

                Comments

                Comment on this article