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DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory
The downstream regulatory element antagonist modulator (DREAM), a multifunctional Ca(2+)-binding protein, binds specifically to DNA and several nucleoproteins regulating gene expression and with proteins outside the nucleus to regulate membrane excitability or calcium homeostasis. DREAM is highly ex...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822766/ https://www.ncbi.nlm.nih.gov/pubmed/20205763 http://dx.doi.org/10.1186/1756-6606-3-3 |
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author | Wu, Long-Jun Mellström, Britt Wang, Hansen Ren, Ming Domingo, Sofia Kim, Susan S Li, Xiang-Yao Chen, Tao Naranjo, Jose R Zhuo, Min |
author_facet | Wu, Long-Jun Mellström, Britt Wang, Hansen Ren, Ming Domingo, Sofia Kim, Susan S Li, Xiang-Yao Chen, Tao Naranjo, Jose R Zhuo, Min |
author_sort | Wu, Long-Jun |
collection | PubMed |
description | The downstream regulatory element antagonist modulator (DREAM), a multifunctional Ca(2+)-binding protein, binds specifically to DNA and several nucleoproteins regulating gene expression and with proteins outside the nucleus to regulate membrane excitability or calcium homeostasis. DREAM is highly expressed in the central nervous system including the hippocampus and cortex; however, the roles of DREAM in hippocampal synaptic transmission and plasticity have not been investigated. Taking advantage of transgenic mice overexpressing a Ca(2+)-insensitive DREAM mutant (TgDREAM), we used integrative methods including electrophysiology, biochemistry, immunostaining, and behavior tests to study the function of DREAM in synaptic transmission, long-term plasticity and fear memory in hippocampal CA1 region. We found that NMDA receptor but not AMPA receptor-mediated current was decreased in TgDREAM mice. Moreover, synaptic plasticity, such as long-term depression (LTD) but not long-term potentiation (LTP), was impaired in TgDREAM mice. Biochemical experiments found that DREAM interacts with PSD-95 and may inhibit NMDA receptor function through this interaction. Contextual fear memory was significantly impaired in TgDREAM mice. By contrast, sensory responses to noxious stimuli were not affected. Our results demonstrate that DREAM plays a novel role in postsynaptic modulation of the NMDA receptor, and contributes to synaptic plasticity and behavioral memory. |
format | Text |
id | pubmed-2822766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28227662010-02-17 DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory Wu, Long-Jun Mellström, Britt Wang, Hansen Ren, Ming Domingo, Sofia Kim, Susan S Li, Xiang-Yao Chen, Tao Naranjo, Jose R Zhuo, Min Mol Brain Research The downstream regulatory element antagonist modulator (DREAM), a multifunctional Ca(2+)-binding protein, binds specifically to DNA and several nucleoproteins regulating gene expression and with proteins outside the nucleus to regulate membrane excitability or calcium homeostasis. DREAM is highly expressed in the central nervous system including the hippocampus and cortex; however, the roles of DREAM in hippocampal synaptic transmission and plasticity have not been investigated. Taking advantage of transgenic mice overexpressing a Ca(2+)-insensitive DREAM mutant (TgDREAM), we used integrative methods including electrophysiology, biochemistry, immunostaining, and behavior tests to study the function of DREAM in synaptic transmission, long-term plasticity and fear memory in hippocampal CA1 region. We found that NMDA receptor but not AMPA receptor-mediated current was decreased in TgDREAM mice. Moreover, synaptic plasticity, such as long-term depression (LTD) but not long-term potentiation (LTP), was impaired in TgDREAM mice. Biochemical experiments found that DREAM interacts with PSD-95 and may inhibit NMDA receptor function through this interaction. Contextual fear memory was significantly impaired in TgDREAM mice. By contrast, sensory responses to noxious stimuli were not affected. Our results demonstrate that DREAM plays a novel role in postsynaptic modulation of the NMDA receptor, and contributes to synaptic plasticity and behavioral memory. BioMed Central 2010-01-21 /pmc/articles/PMC2822766/ /pubmed/20205763 http://dx.doi.org/10.1186/1756-6606-3-3 Text en Copyright ©2010 Wu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wu, Long-Jun Mellström, Britt Wang, Hansen Ren, Ming Domingo, Sofia Kim, Susan S Li, Xiang-Yao Chen, Tao Naranjo, Jose R Zhuo, Min DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title | DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title_full | DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title_fullStr | DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title_full_unstemmed | DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title_short | DREAM (Downstream Regulatory Element Antagonist Modulator) contributes to synaptic depression and contextual fear memory |
title_sort | dream (downstream regulatory element antagonist modulator) contributes to synaptic depression and contextual fear memory |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822766/ https://www.ncbi.nlm.nih.gov/pubmed/20205763 http://dx.doi.org/10.1186/1756-6606-3-3 |
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