Cargando…

Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia

Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA recep...

Descripción completa

Detalles Bibliográficos
Autores principales: Ingason, A, Giegling, I, Hartmann, A M, Genius, J, Konte, B, Friedl, M, Ripke, S, Sullivan, P F, St. Clair, D, Collier, D A, O'Donovan, M C, Mirnics, K, Rujescu, D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930128/
https://www.ncbi.nlm.nih.gov/pubmed/26460480
http://dx.doi.org/10.1038/tp.2015.151
_version_ 1782440700200091648
author Ingason, A
Giegling, I
Hartmann, A M
Genius, J
Konte, B
Friedl, M
Ripke, S
Sullivan, P F
St. Clair, D
Collier, D A
O'Donovan, M C
Mirnics, K
Rujescu, D
author_facet Ingason, A
Giegling, I
Hartmann, A M
Genius, J
Konte, B
Friedl, M
Ripke, S
Sullivan, P F
St. Clair, D
Collier, D A
O'Donovan, M C
Mirnics, K
Rujescu, D
author_sort Ingason, A
collection PubMed
description Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA receptor antagonist MK-801. Subsequently, we performed an expression study and identified 20 genes showing altered expression in the brain of these rats compared with untreated animals. We then explored whether the human orthologs of these genes are associated with schizophrenia in the largest schizophrenia genome-wide association study published to date, and found evidence for association for 4 out of the 20 genes: SF3B1, FOXP1, DLG2 and VGLL4. Interestingly, three of these genes, FOXP1, SF3B1 and DLG2, have previously been implicated in neurodevelopmental disorders.
format Online
Article
Text
id pubmed-4930128
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49301282016-07-14 Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia Ingason, A Giegling, I Hartmann, A M Genius, J Konte, B Friedl, M Ripke, S Sullivan, P F St. Clair, D Collier, D A O'Donovan, M C Mirnics, K Rujescu, D Transl Psychiatry Original Article Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA receptor antagonist MK-801. Subsequently, we performed an expression study and identified 20 genes showing altered expression in the brain of these rats compared with untreated animals. We then explored whether the human orthologs of these genes are associated with schizophrenia in the largest schizophrenia genome-wide association study published to date, and found evidence for association for 4 out of the 20 genes: SF3B1, FOXP1, DLG2 and VGLL4. Interestingly, three of these genes, FOXP1, SF3B1 and DLG2, have previously been implicated in neurodevelopmental disorders. Nature Publishing Group 2015-10 2015-10-13 /pmc/articles/PMC4930128/ /pubmed/26460480 http://dx.doi.org/10.1038/tp.2015.151 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Ingason, A
Giegling, I
Hartmann, A M
Genius, J
Konte, B
Friedl, M
Ripke, S
Sullivan, P F
St. Clair, D
Collier, D A
O'Donovan, M C
Mirnics, K
Rujescu, D
Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title_full Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title_fullStr Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title_full_unstemmed Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title_short Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
title_sort expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930128/
https://www.ncbi.nlm.nih.gov/pubmed/26460480
http://dx.doi.org/10.1038/tp.2015.151
work_keys_str_mv AT ingasona expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT gieglingi expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT hartmannam expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT geniusj expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT konteb expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT friedlm expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT ripkes expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT sullivanpf expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT stclaird expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT collierda expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT odonovanmc expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT mirnicsk expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia
AT rujescud expressionanalysisinaratpsychosismodelidentifiesnovelcandidategenesvalidatedinalargecasecontrolsampleofschizophrenia