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Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system
The disrupted in schizophrenia 1 (DISC1) gene is found at the breakpoint of an inherited chromosomal translocation, and segregates with major mental illnesses. Its potential role in central nervous system (CNS) malfunction has triggered intensive investigation of the biological roles played by DISC1...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232872/ https://www.ncbi.nlm.nih.gov/pubmed/24712987 http://dx.doi.org/10.1111/ejn.12500 |
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author | Randall, Andrew D Kurihara, Mai Brandon, Nicholas J Brown, Jon T |
author_facet | Randall, Andrew D Kurihara, Mai Brandon, Nicholas J Brown, Jon T |
author_sort | Randall, Andrew D |
collection | PubMed |
description | The disrupted in schizophrenia 1 (DISC1) gene is found at the breakpoint of an inherited chromosomal translocation, and segregates with major mental illnesses. Its potential role in central nervous system (CNS) malfunction has triggered intensive investigation of the biological roles played by DISC1, with the hope that this may shed new light on the pathobiology of psychiatric disease. Such work has ranged from investigations of animal behavior to detailed molecular-level analysis of the assemblies that DISC1 forms with other proteins. Here, we discuss the evidence for a role of DISC1 in synaptic function in the mammalian CNS. |
format | Online Article Text |
id | pubmed-4232872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42328722014-12-19 Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system Randall, Andrew D Kurihara, Mai Brandon, Nicholas J Brown, Jon T Eur J Neurosci Special Issue: Synaptic Basis of Disease The disrupted in schizophrenia 1 (DISC1) gene is found at the breakpoint of an inherited chromosomal translocation, and segregates with major mental illnesses. Its potential role in central nervous system (CNS) malfunction has triggered intensive investigation of the biological roles played by DISC1, with the hope that this may shed new light on the pathobiology of psychiatric disease. Such work has ranged from investigations of animal behavior to detailed molecular-level analysis of the assemblies that DISC1 forms with other proteins. Here, we discuss the evidence for a role of DISC1 in synaptic function in the mammalian CNS. BlackWell Publishing Ltd 2014-04 2014-04-08 /pmc/articles/PMC4232872/ /pubmed/24712987 http://dx.doi.org/10.1111/ejn.12500 Text en Copyright © 2014 Federation of European Neuroscience Societies and John Wiley & Sons Ltd http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Special Issue: Synaptic Basis of Disease Randall, Andrew D Kurihara, Mai Brandon, Nicholas J Brown, Jon T Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title | Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title_full | Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title_fullStr | Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title_full_unstemmed | Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title_short | Disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
title_sort | disrupted in schizophrenia 1 and synaptic function in the mammalian central nervous system |
topic | Special Issue: Synaptic Basis of Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232872/ https://www.ncbi.nlm.nih.gov/pubmed/24712987 http://dx.doi.org/10.1111/ejn.12500 |
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