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      SNARE Regulatory Proteins in Synaptic Vesicle Fusion and Recycling

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          Abstract

          Membrane fusion is a universal feature of eukaryotic protein trafficking and is mediated by the soluble N-ethylmaleimide sensitive factor attachment protein receptor (SNARE) family. SNARE proteins embedded in opposing membranes spontaneously assemble to drive membrane fusion and cargo exchange in vitro. Evolution has generated a diverse complement of SNARE regulatory proteins (SRPs) that ensure membrane fusion occurs at the right time and place in vivo. While a core set of SNAREs and SRPs are common to all eukaryotic cells, a specialized set of SRPs within neurons confer additional regulation to synaptic vesicle (SV) fusion. Neuronal communication is characterized by precise spatial and temporal control of SNARE dynamics within presynaptic subdomains specialized for neurotransmitter release. Action potential-elicited Ca 2+ influx at these release sites triggers zippering of SNAREs embedded in the SV and plasma membrane to drive bilayer fusion and release of neurotransmitters that activate downstream targets. Here we discuss current models for how SRPs regulate SNARE dynamics and presynaptic output, emphasizing invertebrate genetic findings that advanced our understanding of SRP regulation of SV cycling.

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          Most cited references392

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          SNAREs--engines for membrane fusion.

          Since the discovery of SNARE proteins in the late 1980s, SNAREs have been recognized as key components of protein complexes that drive membrane fusion. Despite considerable sequence divergence among SNARE proteins, their mechanism seems to be conserved and is adaptable for fusion reactions as diverse as those involved in cell growth, membrane repair, cytokinesis and synaptic transmission. A fascinating picture of these robust nanomachines is emerging.
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            Membrane fusion: grappling with SNARE and SM proteins.

            The two universally required components of the intracellular membrane fusion machinery, SNARE and SM (Sec1/Munc18-like) proteins, play complementary roles in fusion. Vesicular and target membrane-localized SNARE proteins zipper up into an alpha-helical bundle that pulls the two membranes tightly together to exert the force required for fusion. SM proteins, shaped like clasps, bind to trans-SNARE complexes to direct their fusogenic action. Individual fusion reactions are executed by distinct combinations of SNARE and SM proteins to ensure specificity, and are controlled by regulators that embed the SM-SNARE fusion machinery into a physiological context. This regulation is spectacularly apparent in the exquisite speed and precision of synaptic exocytosis, where synaptotagmin (the calcium-ion sensor for fusion) cooperates with complexin (the clamp activator) to control the precisely timed release of neurotransmitters that initiates synaptic transmission and underlies brain function.
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              Rab GTPases as coordinators of vesicle traffic.

              Membrane trafficking between organelles by vesiculotubular carriers is fundamental to the existence of eukaryotic cells. Central in ensuring that cargoes are delivered to their correct destinations are the Rab GTPases, a large family of small GTPases that control membrane identity and vesicle budding, uncoating, motility and fusion through the recruitment of effector proteins, such as sorting adaptors, tethering factors, kinases, phosphatases and motors. Crosstalk between multiple Rab GTPases through shared effectors, or through effectors that recruit selective Rab activators, ensures the spatiotemporal regulation of vesicle traffic. Functional impairments of Rab pathways are associated with diseases, such as immunodeficiencies, cancer and neurological disorders.
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                Author and article information

                Contributors
                Journal
                Front Mol Neurosci
                Front Mol Neurosci
                Front. Mol. Neurosci.
                Frontiers in Molecular Neuroscience
                Frontiers Media S.A.
                1662-5099
                06 August 2021
                2021
                : 14
                : 733138
                Affiliations
                [1] 1The Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology , Cambridge, MA, United States
                [2] 2Department of Biology, Massachusetts Institute of Technology , Cambridge, MA, United States
                Author notes

                Edited by: Zhiyong Shao, Fudan University, China

                Reviewed by: Ege Kavalali, Vanderbilt University, United States; Yongli Zhang, Yale University, United States

                *Correspondence: Chad W. Sauvola, sauvolac@ 123456mit.edu
                J. Troy Littleton, troy@ 123456mit.edu

                This article was submitted to Neuroplasticity and Development, a section of the journal Frontiers in Molecular Neuroscience

                Article
                10.3389/fnmol.2021.733138
                8377282
                34421538
                1cc01e61-319f-4d3b-acbf-a75db21567cd
                Copyright © 2021 Sauvola and Littleton.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
                : 29 June 2021
                : 20 July 2021
                Page count
                Figures: 7, Tables: 1, Equations: 0, References: 392, Pages: 26, Words: 0
                Funding
                Funded by: National Institute of Neurological Disorders and Stroke 10.13039/100000065
                Funded by: National Institute of Mental Health 10.13039/100000025
                Funded by: JPB Foundation 10.13039/100007457
                Categories
                Neuroscience
                Review

                Neurosciences
                snare,synapse,synaptic vesicle,neurotransmitter release,membrane trafficking,drosophila melanogaster,caenorhabditis elegans

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