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Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain

Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and functional changes. Many molecular processes are involved...

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Autores principales: Pronot, Marie, Kieffer, Félicie, Gay, Anne-Sophie, Debayle, Delphine, Forquet, Raphaël, Poupon, Gwénola, Schorova, Lenka, Martin, Stéphane, Gwizdek, Carole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650717/
https://www.ncbi.nlm.nih.gov/pubmed/34887727
http://dx.doi.org/10.3389/fnmol.2021.780535
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author Pronot, Marie
Kieffer, Félicie
Gay, Anne-Sophie
Debayle, Delphine
Forquet, Raphaël
Poupon, Gwénola
Schorova, Lenka
Martin, Stéphane
Gwizdek, Carole
author_facet Pronot, Marie
Kieffer, Félicie
Gay, Anne-Sophie
Debayle, Delphine
Forquet, Raphaël
Poupon, Gwénola
Schorova, Lenka
Martin, Stéphane
Gwizdek, Carole
author_sort Pronot, Marie
collection PubMed
description Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and functional changes. Many molecular processes are involved in this regulation, including post-translational modifications by the Small Ubiquitin-like MOdifier SUMO. To get a wider view of the panel of endogenous synaptic SUMO-modified proteins in the mammalian brain, we combined subcellular fractionation of rat brains at the post-natal day 14 with denaturing immunoprecipitation using SUMO2/3 antibodies and tandem mass spectrometry analysis. Our screening identified 803 candidate SUMO2/3 targets, which represents about 18% of the synaptic proteome. Our dataset includes neurotransmitter receptors, transporters, adhesion molecules, scaffolding proteins as well as vesicular trafficking and cytoskeleton-associated proteins, defining SUMO2/3 as a central regulator of the synaptic organization and function.
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spelling pubmed-86507172021-12-08 Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain Pronot, Marie Kieffer, Félicie Gay, Anne-Sophie Debayle, Delphine Forquet, Raphaël Poupon, Gwénola Schorova, Lenka Martin, Stéphane Gwizdek, Carole Front Mol Neurosci Neuroscience Synapses are highly specialized structures that interconnect neurons to form functional networks dedicated to neuronal communication. During brain development, synapses undergo activity-dependent rearrangements leading to both structural and functional changes. Many molecular processes are involved in this regulation, including post-translational modifications by the Small Ubiquitin-like MOdifier SUMO. To get a wider view of the panel of endogenous synaptic SUMO-modified proteins in the mammalian brain, we combined subcellular fractionation of rat brains at the post-natal day 14 with denaturing immunoprecipitation using SUMO2/3 antibodies and tandem mass spectrometry analysis. Our screening identified 803 candidate SUMO2/3 targets, which represents about 18% of the synaptic proteome. Our dataset includes neurotransmitter receptors, transporters, adhesion molecules, scaffolding proteins as well as vesicular trafficking and cytoskeleton-associated proteins, defining SUMO2/3 as a central regulator of the synaptic organization and function. Frontiers Media S.A. 2021-11-23 /pmc/articles/PMC8650717/ /pubmed/34887727 http://dx.doi.org/10.3389/fnmol.2021.780535 Text en Copyright © 2021 Pronot, Kieffer, Gay, Debayle, Forquet, Poupon, Schorova, Martin and Gwizdek. https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Neuroscience
Pronot, Marie
Kieffer, Félicie
Gay, Anne-Sophie
Debayle, Delphine
Forquet, Raphaël
Poupon, Gwénola
Schorova, Lenka
Martin, Stéphane
Gwizdek, Carole
Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title_full Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title_fullStr Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title_full_unstemmed Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title_short Proteomic Identification of an Endogenous Synaptic SUMOylome in the Developing Rat Brain
title_sort proteomic identification of an endogenous synaptic sumoylome in the developing rat brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650717/
https://www.ncbi.nlm.nih.gov/pubmed/34887727
http://dx.doi.org/10.3389/fnmol.2021.780535
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