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      Liprin-α/SYD-2 determines the size of dense projections in presynaptic active zones in C. elegans

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          Abstract

          Liprin-α/SYD-2 activity promotes the polymerization of electron-dense projections in the presynaptic active zone through increased recruitment of ELKS-1/ELKS.

          Abstract

          Synaptic vesicle (SV) release is spatially and temporally regulated by a network of proteins that form the presynaptic active zone (AZ). The hallmark of most AZs is an electron-dense projection (DP) surrounded by SVs. Despite their importance for our understanding of triggered SV release, high-resolution analyses of DP structures are limited. Using electron microscopy, we show that DPs at Caenorhabditis elegans neuromuscular junctions (NMJs) were highly structured, composed of building units forming bays in which SVs are docked to the AZ membrane. Furthermore, larger ribbonlike DPs that were multimers of the NMJ building unit are found at synapses between inter- and motoneurons. We also demonstrate that DP size is determined by the activity of the AZ protein SYD-2/Liprin-α. Whereas loss of syd-2 function led to smaller DPs, syd-2 gain-of-function mutants displayed larger ribbonlike DPs through increased recruitment of ELKS-1/ELKS. Therefore, our data suggest that a main role of SYD-2/Liprin-α in synaptogenesis is to regulate the polymerization of DPs.

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          Most cited references45

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          Maturation of active zone assembly by Drosophila Bruchpilot

          Synaptic vesicles fuse at active zone (AZ) membranes where Ca2+ channels are clustered and that are typically decorated by electron-dense projections. Recently, mutants of the Drosophila melanogaster ERC/CAST family protein Bruchpilot (BRP) were shown to lack dense projections (T-bars) and to suffer from Ca2+ channel–clustering defects. In this study, we used high resolution light microscopy, electron microscopy, and intravital imaging to analyze the function of BRP in AZ assembly. Consistent with truncated BRP variants forming shortened T-bars, we identify BRP as a direct T-bar component at the AZ center with its N terminus closer to the AZ membrane than its C terminus. In contrast, Drosophila Liprin-α, another AZ-organizing protein, precedes BRP during the assembly of newly forming AZs by several hours and surrounds the AZ center in few discrete punctae. BRP seems responsible for effectively clustering Ca2+ channels beneath the T-bar density late in a protracted AZ formation process, potentially through a direct molecular interaction with intracellular Ca2+ channel domains.
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            RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone.

            Neurotransmitters are released by synaptic vesicle fusion at the active zone. The active zone of a synapse mediates Ca2+-triggered neurotransmitter release, and integrates presynaptic signals in regulating this release. Much is known about the structure of active zones and synaptic vesicles, but the functional relation between their components is poorly understood. Here we show that RIM1alpha, an active zone protein that was identified as a putative effector for the synaptic vesicle protein Rab3A, interacts with several active zone molecules, including Munc13-1 (ref. 6) and alpha-liprins, to form a protein scaffold in the presynaptic nerve terminal. Abolishing the expression of RIM1alpha in mice shows that RIM1alpha is essential for maintaining normal probability of neurotransmitter release, and for regulating release during short-term synaptic plasticity. These data indicate that RIM1alpha has a central function in integrating active zone proteins and synaptic vesicles into a molecular scaffold that controls neurotransmitter release.
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              Systematic analysis of genes required for synapse structure and function.

              Chemical synapses are complex structures that mediate rapid intercellular signalling in the nervous system. Proteomic studies suggest that several hundred proteins will be found at synaptic specializations. Here we describe a systematic screen to identify genes required for the function or development of Caenorhabditis elegans neuromuscular junctions. A total of 185 genes were identified in an RNA interference screen for decreased acetylcholine secretion; 132 of these genes had not previously been implicated in synaptic transmission. Functional profiles for these genes were determined by comparing secretion defects observed after RNA interference under a variety of conditions. Hierarchical clustering identified groups of functionally related genes, including those involved in the synaptic vesicle cycle, neuropeptide signalling and responsiveness to phorbol esters. Twenty-four genes encoded proteins that were localized to presynaptic specializations. Loss-of-function mutations in 12 genes caused defects in presynaptic structure.
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                Author and article information

                Journal
                J Cell Biol
                J. Cell Biol
                jcb
                The Journal of Cell Biology
                The Rockefeller University Press
                0021-9525
                1540-8140
                9 December 2013
                : 203
                : 5
                : 849-863
                Affiliations
                [1 ]European Neuroscience Institute, 37077 Göttingen, Germany
                [2 ]Cellular Neurobiology, Schwann-Schleiden-Centre for Molecular Cell Biology, 37077 Göttingen, Germany
                [3 ]Center for Molecular Physiology of the Brain, 37073 Göttingen, Germany
                [4 ]Institute of Functional and Applied Anatomy, Hannover Medical School, 30625 Hannover, Germany
                [5 ]Howard Hughes Medical Institute, Division of Biological Sciences ; and [6 ]Center for Research on Biological Systems, National Center for Microscopy and Imaging Research and Department of Neurosciences; University of California, San Diego, La Jolla, CA 92093
                [7 ]Laboratory of Neuronal Cell Biology, Graduate School of Pharmaceutical Sciences and Creative Research Institute, Hokkaido University, Kita-ku, Sapporo 060-0812, Japan
                [8 ]Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL 60607
                [9 ]BIOSS Centre for Biological Signalling Studies, University of Freiburg, 79108 Freiburg, Germany
                Author notes
                Correspondence to Stefan Eimer: seimer@ 123456gwdg.de

                M. Kittelmann and J. Hegermann contributed equally to this paper.

                Article
                201302022
                10.1083/jcb.201302022
                3857474
                24322429
                0c70ee85-7c19-40c5-8292-60c1bb329870
                © 2013 Kittelmann et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

                History
                : 5 February 2013
                : 6 November 2013
                Categories
                Research Articles
                Article

                Cell biology
                Cell biology

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