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      Role of Bassoon and Piccolo in Assembly and Molecular Organization of the Active Zone

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          Abstract

          Bassoon and Piccolo are two very large scaffolding proteins of the cytomatrix assembled at the active zone (CAZ) where neurotransmitter is released. They share regions of high sequence similarity distributed along their entire length and seem to share both overlapping and distinct functions in organizing the CAZ. Here, we survey our present knowledge on protein-protein interactions and recent progress in understanding of molecular functions of these two giant proteins. These include roles in the assembly of active zones (AZ), the localization of voltage-gated Ca 2+ channels (VGCCs) in the vicinity of release sites, synaptic vesicle (SV) priming and in the case of Piccolo, a role in the dynamic assembly of the actin cytoskeleton. Piccolo and Bassoon are also important for the maintenance of presynaptic structure and function, as well as for the assembly of CAZ specializations such as synaptic ribbons. Recent findings suggest that they are also involved in the regulation activity-dependent communication between presynaptic boutons and the neuronal nucleus. Together these observations suggest that Bassoon and Piccolo use their modular structure to organize super-molecular complexes essential for various aspects of presynaptic function.

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          Most cited references113

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          Ultrafast endocytosis at mouse hippocampal synapses

          To sustain neurotransmission, synaptic vesicles and their associated proteins must be recycled locally at synapses. Synaptic vesicles are thought to be regenerated ~20 s after fusion by the assembly of clathrin scaffolds or in ~1 s by the reversal of fusion pores via ‘kiss-and-run’ endocytosis. Here we use optogenetics to stimulate cultured hippocampal neurons with a single stimulus, rapidly freeze them after fixed intervals and examine the ultrastructure using electron microscopy – ‘flash-and-freeze’ electron microscopy. Docked vesicles fuse and collapse into the membrane within 30 ms of the stimulus. Compensatory endocytosis occurs with 50-100 ms at sites flanking the active zone. Invagination is blocked by inhibition of actin polymerization, and scission is blocked by inhibiting dynamin. Because intact synaptic vesicles are not recovered, this form of recycling is not compatible with kiss-and-run endocytosis; moreover it is 200-fold faster than clathrin-mediated endocytosis. It is likely that ‘ultrafast endocytosis’ is specialized to rapidly restore the surface area of the membrane.
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            Hair cell synaptic ribbons are essential for synchronous auditory signalling.

            Hearing relies on faithful synaptic transmission at the ribbon synapse of cochlear inner hair cells (IHCs). At present, the function of presynaptic ribbons at these synapses is still largely unknown. Here we show that anchoring of IHC ribbons is impaired in mouse mutants for the presynaptic scaffolding protein Bassoon. The lack of active-zone-anchored synaptic ribbons reduced the presynaptic readily releasable vesicle pool, and impaired synchronous auditory signalling as revealed by recordings of exocytic IHC capacitance changes and sound-evoked activation of spiral ganglion neurons. Both exocytosis of the hair cell releasable vesicle pool and the number of synchronously activated spiral ganglion neurons co-varied with the number of anchored ribbons during development. Interestingly, ribbon-deficient IHCs were still capable of sustained exocytosis with normal Ca2+-dependence. Endocytic membrane retrieval was intact, but an accumulation of tubular and cisternal membrane profiles was observed in ribbon-deficient IHCs. We conclude that ribbon-dependent synchronous release of multiple vesicles at the hair cell afferent synapse is essential for normal hearing.
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              RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone.

              At presynaptic active zones, neurotransmitter release is initiated by the opening of voltage-gated Ca²+ channels close to docked vesicles. The mechanisms that enrich Ca²+ channels at active zones are, however, largely unknown, possibly because of the limited presynaptic accessibility of most synapses. Here, we have established a Cre-lox based conditional knockout approach at a presynaptically accessible central nervous system synapse, the calyx of Held, to directly study the functions of RIM proteins. Removal of all RIM1/2 isoforms strongly reduced the presynaptic Ca²+ channel density, revealing a role of RIM proteins in Ca²+ channel targeting. Removal of RIMs also reduced the readily releasable pool, paralleled by a similar reduction of the number of docked vesicles, and the Ca²+ channel-vesicle coupling was decreased. Thus, RIM proteins co-ordinately regulate key functions for fast transmitter release, enabling a high presynaptic Ca²+ channel density and vesicle docking at the active zone. © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Synaptic Neurosci
                Front Synaptic Neurosci
                Front. Synaptic Neurosci.
                Frontiers in Synaptic Neuroscience
                Frontiers Media S.A.
                1663-3563
                12 January 2016
                2015
                : 7
                : 19
                Affiliations
                [1] 1Department Neurochemistry and Molecular Biology, Leibniz Institute for Neurobiology Magdeburg, Germany
                [2] 2Center for Behavioral Brain Sciences Magdeburg, Germany
                [3] 3Medical Faculty, Otto von Guericke University Magdeburg, Germany
                [4] 4German Center for Neurodegenerative Diseases (DZNE) Site Magdeburg Magdeburg, Germany
                [5] 5Institute of Anatomy and Molecular Neurobiology, Westfälische Wilhelms University Münster, Germany
                [6] 6German Center for Neurodegenerative Diseases (DZNE) Site Berlin Berlin, Germany
                [7] 7Charité Medical University Berlin, Germany
                Author notes

                Edited by: Lucia Tabares, University of Seville, Spain

                Reviewed by: Carlo Sala, CNR Institute of Neuroscience, Italy; Hiroshi Nishimune, University of Kansas Medical School, USA

                *Correspondence: Eckart D. Gundelfinger gundelfi@ 123456lin-magdeburg.de ; Craig C. Garner craig-curtis.garner@ 123456dzne.de
                Article
                10.3389/fnsyn.2015.00019
                4709825
                26793095
                319275a5-2875-4546-ad39-f217cb8c4cc2
                Copyright © 2016 Gundelfinger, Reissner and Garner.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 10 November 2015
                : 14 December 2015
                Page count
                Figures: 1, Tables: 1, Equations: 0, References: 127, Pages: 11, Words: 8846
                Categories
                Neuroscience
                Review

                Neurosciences
                bassoon,piccolo,aczonin,cytomatrix at the active zone,neurotransmitter release,synapto-nuclear signaling,actin dynamics,synaptic vesicle

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