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The natural Disc1-deletion present in several inbred mouse strains does not affect sleep
The gene Disrupted in Schizophrenia-1 (DISC1) is linked to a range of psychiatric disorders. Two recent transgenic studies suggest DISC1 is also involved in homeostatic sleep regulation. Several strains of inbred mice commonly used for genome manipulation experiments, including several Swiss and lik...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515846/ https://www.ncbi.nlm.nih.gov/pubmed/28720848 http://dx.doi.org/10.1038/s41598-017-06015-3 |
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author | Dittrich, Lars Petese, Alessandro Jackson, Walker S. |
author_facet | Dittrich, Lars Petese, Alessandro Jackson, Walker S. |
author_sort | Dittrich, Lars |
collection | PubMed |
description | The gene Disrupted in Schizophrenia-1 (DISC1) is linked to a range of psychiatric disorders. Two recent transgenic studies suggest DISC1 is also involved in homeostatic sleep regulation. Several strains of inbred mice commonly used for genome manipulation experiments, including several Swiss and likely all 129 substrains, carry a natural deletion mutation of Disc1. This constitutes a potential confound for studying sleep in genetically modified mice. Since disturbed sleep can also influence psychiatric and neurodegenerative disease models, this putative confound might affect a wide range of studies in several fields. Therefore, we asked to what extent the natural Disc1 deletion affects sleep. To this end, we first compared sleep and electroencephalogram (EEG) phenotypes of 129S4 mice carrying the Disc1 deletion and C57BL/6N mice carrying the full-length version. We then bred Disc1 from C57BL/6N into the 129S4 background, resulting in S4-Disc1 mice. The differences between 129S4 and C57BL/6N were not detected in the 129S4 to S4-Disc1 comparison. We conclude that the mutation has no effect on the measured sleep and EEG characteristics. Thus, it is unlikely the widespread Disc1 deletion has led to spurious results in previous sleep studies or that it alters sleep in mouse models of psychiatric or neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-5515846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55158462017-07-19 The natural Disc1-deletion present in several inbred mouse strains does not affect sleep Dittrich, Lars Petese, Alessandro Jackson, Walker S. Sci Rep Article The gene Disrupted in Schizophrenia-1 (DISC1) is linked to a range of psychiatric disorders. Two recent transgenic studies suggest DISC1 is also involved in homeostatic sleep regulation. Several strains of inbred mice commonly used for genome manipulation experiments, including several Swiss and likely all 129 substrains, carry a natural deletion mutation of Disc1. This constitutes a potential confound for studying sleep in genetically modified mice. Since disturbed sleep can also influence psychiatric and neurodegenerative disease models, this putative confound might affect a wide range of studies in several fields. Therefore, we asked to what extent the natural Disc1 deletion affects sleep. To this end, we first compared sleep and electroencephalogram (EEG) phenotypes of 129S4 mice carrying the Disc1 deletion and C57BL/6N mice carrying the full-length version. We then bred Disc1 from C57BL/6N into the 129S4 background, resulting in S4-Disc1 mice. The differences between 129S4 and C57BL/6N were not detected in the 129S4 to S4-Disc1 comparison. We conclude that the mutation has no effect on the measured sleep and EEG characteristics. Thus, it is unlikely the widespread Disc1 deletion has led to spurious results in previous sleep studies or that it alters sleep in mouse models of psychiatric or neurodegenerative diseases. Nature Publishing Group UK 2017-07-18 /pmc/articles/PMC5515846/ /pubmed/28720848 http://dx.doi.org/10.1038/s41598-017-06015-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dittrich, Lars Petese, Alessandro Jackson, Walker S. The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title | The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title_full | The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title_fullStr | The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title_full_unstemmed | The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title_short | The natural Disc1-deletion present in several inbred mouse strains does not affect sleep |
title_sort | natural disc1-deletion present in several inbred mouse strains does not affect sleep |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515846/ https://www.ncbi.nlm.nih.gov/pubmed/28720848 http://dx.doi.org/10.1038/s41598-017-06015-3 |
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