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

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posted on 2025-05-11, 11:24 authored by A. Ingason, I. Giegling, D. A. Collier, M. C. O'Donovan, K. Mirnics, D. Rujescu, Frans HenskensFrans Henskens, Murray CairnsMurray Cairns, Brian KellyBrian Kelly, Carmel LoughlandCarmel Loughland, Ulrich Schall, Rodney ScottRodney Scott, A. M. Hartmann, Paul TooneyPaul Tooney, Patricia MichiePatricia Michie, Jing Qin Wu, J. Genius, B. Konte, M. Friedl, Schizophrenia Working Group of the Psychiatric Genomics Consortium (PGC), S. Ripke, P. F. Sullivan, D. St. Clair
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.

History

Journal title

Translational Psychiatry

Volume

5

Issue

10

Pagination

e656-e656

Publisher

Nature Publishing

Language

  • en, English

College/Research Centre

Faculty of Health and Medicine

School

Priority Research Centre for Health Behaviour

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