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CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory

Regulated RNA translation is critical to provide proteins needed to maintain persistent modification of synaptic strength, which underlies the molecular basis of long-term memory (LTM). Cytoplasmic polyadenylation element-binding proteins (CPEBs) are sequence-specific RNA-binding proteins and regula...

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Autores principales: Tsai, Li-Yun, Chang, Yu-Wei, Lin, Pei-Yi, Chou, Hsin-Jung, Liu, Ta-Jen, Lee, Ping-Tao, Huang, Wen-Hsuan, Tsou, Yueh-Liang, Huang, Yi-Shuian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875571/
https://www.ncbi.nlm.nih.gov/pubmed/24386439
http://dx.doi.org/10.1371/journal.pone.0084978
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author Tsai, Li-Yun
Chang, Yu-Wei
Lin, Pei-Yi
Chou, Hsin-Jung
Liu, Ta-Jen
Lee, Ping-Tao
Huang, Wen-Hsuan
Tsou, Yueh-Liang
Huang, Yi-Shuian
author_facet Tsai, Li-Yun
Chang, Yu-Wei
Lin, Pei-Yi
Chou, Hsin-Jung
Liu, Ta-Jen
Lee, Ping-Tao
Huang, Wen-Hsuan
Tsou, Yueh-Liang
Huang, Yi-Shuian
author_sort Tsai, Li-Yun
collection PubMed
description Regulated RNA translation is critical to provide proteins needed to maintain persistent modification of synaptic strength, which underlies the molecular basis of long-term memory (LTM). Cytoplasmic polyadenylation element-binding proteins (CPEBs) are sequence-specific RNA-binding proteins and regulate translation in various tissues. All four CPEBs in vertebrates are expressed in the brain, including the hippocampal neurons, suggesting their potential roles in translation-dependent plasticity and memory. Although CPEB1 and CPEB3 have been shown to control specific kinds of hippocampus-related LTM, the role of CPEB2 and CPEB4 in learning and memory remains elusive. Thus, we generated CPEB4 knockout (KO) mice and analyzed them using several behavioral tests. No difference was found in the anxiety level, motor coordination, hippocampus-dependent learning and memory between the KO mice and their wild-type (WT) littermates. Electrophysiological recordings of multiple forms of synaptic plasticity in the Schaffer collateral pathway-CA1 neurons also showed normal responses in the KO hippocampal slices. Morphological analyses revealed that the CPEB4-lacking pyramidal neurons possessed slightly elongated dendritic spines. Unlike its related family members, CPEB1 and CPEB3, CPEB4 seems to be dispensable for hippocampus-dependent plasticity, learning and memory.
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spelling pubmed-38755712014-01-02 CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory Tsai, Li-Yun Chang, Yu-Wei Lin, Pei-Yi Chou, Hsin-Jung Liu, Ta-Jen Lee, Ping-Tao Huang, Wen-Hsuan Tsou, Yueh-Liang Huang, Yi-Shuian PLoS One Research Article Regulated RNA translation is critical to provide proteins needed to maintain persistent modification of synaptic strength, which underlies the molecular basis of long-term memory (LTM). Cytoplasmic polyadenylation element-binding proteins (CPEBs) are sequence-specific RNA-binding proteins and regulate translation in various tissues. All four CPEBs in vertebrates are expressed in the brain, including the hippocampal neurons, suggesting their potential roles in translation-dependent plasticity and memory. Although CPEB1 and CPEB3 have been shown to control specific kinds of hippocampus-related LTM, the role of CPEB2 and CPEB4 in learning and memory remains elusive. Thus, we generated CPEB4 knockout (KO) mice and analyzed them using several behavioral tests. No difference was found in the anxiety level, motor coordination, hippocampus-dependent learning and memory between the KO mice and their wild-type (WT) littermates. Electrophysiological recordings of multiple forms of synaptic plasticity in the Schaffer collateral pathway-CA1 neurons also showed normal responses in the KO hippocampal slices. Morphological analyses revealed that the CPEB4-lacking pyramidal neurons possessed slightly elongated dendritic spines. Unlike its related family members, CPEB1 and CPEB3, CPEB4 seems to be dispensable for hippocampus-dependent plasticity, learning and memory. Public Library of Science 2013-12-30 /pmc/articles/PMC3875571/ /pubmed/24386439 http://dx.doi.org/10.1371/journal.pone.0084978 Text en © 2013 Tsai et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tsai, Li-Yun
Chang, Yu-Wei
Lin, Pei-Yi
Chou, Hsin-Jung
Liu, Ta-Jen
Lee, Ping-Tao
Huang, Wen-Hsuan
Tsou, Yueh-Liang
Huang, Yi-Shuian
CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title_full CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title_fullStr CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title_full_unstemmed CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title_short CPEB4 Knockout Mice Exhibit Normal Hippocampus-Related Synaptic Plasticity and Memory
title_sort cpeb4 knockout mice exhibit normal hippocampus-related synaptic plasticity and memory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875571/
https://www.ncbi.nlm.nih.gov/pubmed/24386439
http://dx.doi.org/10.1371/journal.pone.0084978
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