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Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour

Genes responsible for generating circadian oscillations are expressed in a variety of brain regions not typically associated with circadian timing. The functions of this clock gene expression are largely unknown, and in the present study we sought to explore the role of the Per2 (Period 2) gene in h...

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Autores principales: Wang, Louisa M-C, Dragich, Joanna M, Kudo, Takashi, Odom, Irene H, Welsh, David K, O'Dell, Thomas J, Colwell, Christopher S
Formato: Texto
Lenguaje:English
Publicado: American Society for Neurochemistry 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695588/
https://www.ncbi.nlm.nih.gov/pubmed/19570032
http://dx.doi.org/10.1042/AN20090020
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author Wang, Louisa M-C
Dragich, Joanna M
Kudo, Takashi
Odom, Irene H
Welsh, David K
O'Dell, Thomas J
Colwell, Christopher S
author_facet Wang, Louisa M-C
Dragich, Joanna M
Kudo, Takashi
Odom, Irene H
Welsh, David K
O'Dell, Thomas J
Colwell, Christopher S
author_sort Wang, Louisa M-C
collection PubMed
description Genes responsible for generating circadian oscillations are expressed in a variety of brain regions not typically associated with circadian timing. The functions of this clock gene expression are largely unknown, and in the present study we sought to explore the role of the Per2 (Period 2) gene in hippocampal physiology and learned behaviour. We found that PER2 protein is highly expressed in hippocampal pyramidal cell layers and that the expression of both protein and mRNA varies with a circadian rhythm. The peaks of these rhythms occur in the late night or early morning and are almost 180° out-of-phase with the expression rhythms measured from the suprachiasmatic nucleus of the same animals. The rhythms in Per2 expression are autonomous as they are present in isolated hippocampal slices maintained in culture. Physiologically, Per2-mutant mice exhibit abnormal long-term potentiation. The underlying mechanism is suggested by the finding that levels of phosphorylated cAMP-response-element-binding protein, but not phosphorylated extracellular-signal-regulated kinase, are reduced in hippocampal tissue from mutant mice. Finally, Per2-mutant mice exhibit deficits in the recall of trace, but not cued, fear conditioning. Taken together, these results provide evidence that hippocampal cells contain an autonomous circadian clock. Furthermore, the clock gene Per2 may play a role in the regulation of long-term potentiation and in the recall of some forms of learned behaviour.
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spelling pubmed-26955882009-06-23 Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour Wang, Louisa M-C Dragich, Joanna M Kudo, Takashi Odom, Irene H Welsh, David K O'Dell, Thomas J Colwell, Christopher S ASN Neuro Research Article Genes responsible for generating circadian oscillations are expressed in a variety of brain regions not typically associated with circadian timing. The functions of this clock gene expression are largely unknown, and in the present study we sought to explore the role of the Per2 (Period 2) gene in hippocampal physiology and learned behaviour. We found that PER2 protein is highly expressed in hippocampal pyramidal cell layers and that the expression of both protein and mRNA varies with a circadian rhythm. The peaks of these rhythms occur in the late night or early morning and are almost 180° out-of-phase with the expression rhythms measured from the suprachiasmatic nucleus of the same animals. The rhythms in Per2 expression are autonomous as they are present in isolated hippocampal slices maintained in culture. Physiologically, Per2-mutant mice exhibit abnormal long-term potentiation. The underlying mechanism is suggested by the finding that levels of phosphorylated cAMP-response-element-binding protein, but not phosphorylated extracellular-signal-regulated kinase, are reduced in hippocampal tissue from mutant mice. Finally, Per2-mutant mice exhibit deficits in the recall of trace, but not cued, fear conditioning. Taken together, these results provide evidence that hippocampal cells contain an autonomous circadian clock. Furthermore, the clock gene Per2 may play a role in the regulation of long-term potentiation and in the recall of some forms of learned behaviour. American Society for Neurochemistry 2009-06-10 /pmc/articles/PMC2695588/ /pubmed/19570032 http://dx.doi.org/10.1042/AN20090020 Text en © 2009 The Author(s). http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commerical use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Louisa M-C
Dragich, Joanna M
Kudo, Takashi
Odom, Irene H
Welsh, David K
O'Dell, Thomas J
Colwell, Christopher S
Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title_full Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title_fullStr Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title_full_unstemmed Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title_short Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
title_sort expression of the circadian clock gene period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695588/
https://www.ncbi.nlm.nih.gov/pubmed/19570032
http://dx.doi.org/10.1042/AN20090020
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