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Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning

Genes involved in synaptic plasticity, particularly genes encoding postsynaptic density proteins, have been recurrently linked to psychiatric disorders including schizophrenia and autism. Postsynaptic density Homer1 proteins contribute to synaptic plasticity through the competing actions of short an...

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Autores principales: Clifton, Nicholas E., Cameron, Darren, Trent, Simon, Sykes, Lucy H., Thomas, Kerrie L., Hall, Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697134/
https://www.ncbi.nlm.nih.gov/pubmed/29238619
http://dx.doi.org/10.1155/2017/5959182
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author Clifton, Nicholas E.
Cameron, Darren
Trent, Simon
Sykes, Lucy H.
Thomas, Kerrie L.
Hall, Jeremy
author_facet Clifton, Nicholas E.
Cameron, Darren
Trent, Simon
Sykes, Lucy H.
Thomas, Kerrie L.
Hall, Jeremy
author_sort Clifton, Nicholas E.
collection PubMed
description Genes involved in synaptic plasticity, particularly genes encoding postsynaptic density proteins, have been recurrently linked to psychiatric disorders including schizophrenia and autism. Postsynaptic density Homer1 proteins contribute to synaptic plasticity through the competing actions of short and long isoforms. The activity-induced expression of short Homer1 isoforms, Homer1a and Ania-3, is thought to be related to processes of learning and memory. However, the precise regulation of Homer1a and Ania-3 with different components of learning has not been investigated. Here, we used in situ hybridization to quantify short and long Homer1 expression in the hippocampus following consolidation, retrieval, and extinction of associative fear memory, using contextual fear conditioning in rats. Homer1a and Ania-3, but not long Homer1, were regulated by contextual fear learning or novelty detection, although their precise patterns of expression in hippocampal subregions were dependent on the isoform. We also show for the first time that the two short Homer1 isoforms are regulated after the retrieval and extinction of contextual fear memory, albeit with distinct temporal and spatial profiles. These findings support a role of activity-induced Homer1 isoforms in learning and memory processes in discrete hippocampal subregions and suggest that Homer1a and Ania-3 may play separable roles in synaptic plasticity.
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spelling pubmed-56971342017-12-13 Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning Clifton, Nicholas E. Cameron, Darren Trent, Simon Sykes, Lucy H. Thomas, Kerrie L. Hall, Jeremy Neural Plast Research Article Genes involved in synaptic plasticity, particularly genes encoding postsynaptic density proteins, have been recurrently linked to psychiatric disorders including schizophrenia and autism. Postsynaptic density Homer1 proteins contribute to synaptic plasticity through the competing actions of short and long isoforms. The activity-induced expression of short Homer1 isoforms, Homer1a and Ania-3, is thought to be related to processes of learning and memory. However, the precise regulation of Homer1a and Ania-3 with different components of learning has not been investigated. Here, we used in situ hybridization to quantify short and long Homer1 expression in the hippocampus following consolidation, retrieval, and extinction of associative fear memory, using contextual fear conditioning in rats. Homer1a and Ania-3, but not long Homer1, were regulated by contextual fear learning or novelty detection, although their precise patterns of expression in hippocampal subregions were dependent on the isoform. We also show for the first time that the two short Homer1 isoforms are regulated after the retrieval and extinction of contextual fear memory, albeit with distinct temporal and spatial profiles. These findings support a role of activity-induced Homer1 isoforms in learning and memory processes in discrete hippocampal subregions and suggest that Homer1a and Ania-3 may play separable roles in synaptic plasticity. Hindawi 2017 2017-11-07 /pmc/articles/PMC5697134/ /pubmed/29238619 http://dx.doi.org/10.1155/2017/5959182 Text en Copyright © 2017 Nicholas E. Clifton et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Clifton, Nicholas E.
Cameron, Darren
Trent, Simon
Sykes, Lucy H.
Thomas, Kerrie L.
Hall, Jeremy
Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title_full Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title_fullStr Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title_full_unstemmed Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title_short Hippocampal Regulation of Postsynaptic Density Homer1 by Associative Learning
title_sort hippocampal regulation of postsynaptic density homer1 by associative learning
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697134/
https://www.ncbi.nlm.nih.gov/pubmed/29238619
http://dx.doi.org/10.1155/2017/5959182
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