Schizophrenia copy number variants and associative learning
| Autor: | N E, Clifton, A J, Pocklington, B, Scholz, E, Rees, J T R, Walters, G, Kirov, M C, O'Donovan, M J, Owen, L S, Wilkinson, K L, Thomas, J, Hall |
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| Rok vydání: | 2016 |
| Předmět: |
Male
congenital hereditary and neonatal diseases and abnormalities endocrine system diseases DNA Copy Number Variations Databases Factual Conditioning Classical Association Learning Fear behavioral disciplines and activities Rats Case-Control Studies mental disorders Schizophrenia Animals Humans Female Genetic Predisposition to Disease Immediate Communication CA1 Region Hippocampal Genome-Wide Association Study |
| Zdroj: | Molecular Psychiatry |
| ISSN: | 1476-5578 |
| Popis: | Large-scale genomic studies have made major progress in identifying genetic risk variants for schizophrenia. A key finding from these studies is that there is an increased burden of genomic copy number variants (CNVs) in schizophrenia cases compared with controls. The mechanism through which these CNVs confer risk for the symptoms of schizophrenia, however, remains unclear. One possibility is that schizophrenia risk CNVs impact basic associative learning processes, abnormalities of which have long been associated with the disorder. To investigate whether genes in schizophrenia CNVs impact on specific phases of associative learning we combined human genetics with experimental gene expression studies in animals. In a sample of 11 917 schizophrenia cases and 16 416 controls, we investigated whether CNVs from patients with schizophrenia are enriched for genes expressed during the consolidation, retrieval or extinction of associative memories. We show that CNVs from cases are enriched for genes expressed during fear extinction in the hippocampus, but not genes expressed following consolidation or retrieval. These results suggest that CNVs act to impair inhibitory learning in schizophrenia, potentially contributing to the development of core symptoms of the disorder. |
| Databáze: | OpenAIRE |
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