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Role of the visual experience-dependent nascent proteome in neuronal plasticity
Experience-dependent synaptic plasticity refines brain circuits during development. To identify novel protein synthesis-dependent mechanisms contributing to experience-dependent plasticity, we conducted a quantitative proteomic screen of the nascent proteome in response to visual experience in Xenop...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815848/ https://www.ncbi.nlm.nih.gov/pubmed/29412139 http://dx.doi.org/10.7554/eLife.33420 |
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author | Liu, Han-Hsuan McClatchy, Daniel B Schiapparelli, Lucio Shen, Wanhua Yates, John R Cline, Hollis T |
author_facet | Liu, Han-Hsuan McClatchy, Daniel B Schiapparelli, Lucio Shen, Wanhua Yates, John R Cline, Hollis T |
author_sort | Liu, Han-Hsuan |
collection | PubMed |
description | Experience-dependent synaptic plasticity refines brain circuits during development. To identify novel protein synthesis-dependent mechanisms contributing to experience-dependent plasticity, we conducted a quantitative proteomic screen of the nascent proteome in response to visual experience in Xenopus optic tectum using bio-orthogonal metabolic labeling (BONCAT). We identified 83 differentially synthesized candidate plasticity proteins (CPPs). The CPPs form strongly interconnected networks and are annotated to a variety of biological functions, including RNA splicing, protein translation, and chromatin remodeling. Functional analysis of select CPPs revealed the requirement for eukaryotic initiation factor three subunit A (eIF3A), fused in sarcoma (FUS), and ribosomal protein s17 (RPS17) in experience-dependent structural plasticity in tectal neurons and behavioral plasticity in tadpoles. These results demonstrate that the nascent proteome is dynamic in response to visual experience and that de novo synthesis of machinery that regulates RNA splicing and protein translation is required for experience-dependent plasticity. |
format | Online Article Text |
id | pubmed-5815848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58158482018-02-22 Role of the visual experience-dependent nascent proteome in neuronal plasticity Liu, Han-Hsuan McClatchy, Daniel B Schiapparelli, Lucio Shen, Wanhua Yates, John R Cline, Hollis T eLife Neuroscience Experience-dependent synaptic plasticity refines brain circuits during development. To identify novel protein synthesis-dependent mechanisms contributing to experience-dependent plasticity, we conducted a quantitative proteomic screen of the nascent proteome in response to visual experience in Xenopus optic tectum using bio-orthogonal metabolic labeling (BONCAT). We identified 83 differentially synthesized candidate plasticity proteins (CPPs). The CPPs form strongly interconnected networks and are annotated to a variety of biological functions, including RNA splicing, protein translation, and chromatin remodeling. Functional analysis of select CPPs revealed the requirement for eukaryotic initiation factor three subunit A (eIF3A), fused in sarcoma (FUS), and ribosomal protein s17 (RPS17) in experience-dependent structural plasticity in tectal neurons and behavioral plasticity in tadpoles. These results demonstrate that the nascent proteome is dynamic in response to visual experience and that de novo synthesis of machinery that regulates RNA splicing and protein translation is required for experience-dependent plasticity. eLife Sciences Publications, Ltd 2018-02-07 /pmc/articles/PMC5815848/ /pubmed/29412139 http://dx.doi.org/10.7554/eLife.33420 Text en © 2018, Liu et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Liu, Han-Hsuan McClatchy, Daniel B Schiapparelli, Lucio Shen, Wanhua Yates, John R Cline, Hollis T Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title | Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title_full | Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title_fullStr | Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title_full_unstemmed | Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title_short | Role of the visual experience-dependent nascent proteome in neuronal plasticity |
title_sort | role of the visual experience-dependent nascent proteome in neuronal plasticity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815848/ https://www.ncbi.nlm.nih.gov/pubmed/29412139 http://dx.doi.org/10.7554/eLife.33420 |
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