Finding causal variants within schizophrenia risk loci

Project: Research project

Description

Schizophrenia is highly heritable and the cause of substantial morbidity, mortality, and personal and societal costs. To increase our understanding of the biological basis of schizophrenia, it is essential to identify precise causal mutations that influence risk. GWAS have been remarkably successful in identifying genomic regions harboring common SNPs associated with schizophrenia. The most recent PGC analysis yielded 128 genome-wide significant loci and this number will likely increase. However, the causative variants underlying nearly all GWAS loci have proven elusive. Existing imputation resources are not optimized for GWAS loci. The overarching goal of this proposal is to identify causative mutations within schizophrenia GWAS loci. Common risk loci resulting from changes in copy number (i.e., copy number polymorphism, or CNP) are attractive casual mutations. CNPs that reside within GWAS loci (i.e., “tagged” by the associated SNPs) can alter the dosage or structure of regulatory elements and genes and exert functional impact to drive the observed association with SCZ. Multiple examples are in the literature. The contribution of CNPs to schizophrenia is unknown because large-scale surveys of CNPs have not been done. CNPs are inaccessible to most current methods, and CNP imputation methods are underdeveloped. Since CNPs are highly plausible but largely unexplored, we propose to deeply sequence schizophrenia samples at the PGC GWAS loci to identify CNPs and uncommon single nucleotide variants (SNVs), and then impute them into very large samples to test for association with schizophrenia. Identifying uncommon SNVs maximizes expenditure of the proposed study. Successful completion of the proposed work will enhance our understanding of biological mechanisms underlying the etiology of schizophrenia. If we can identify even a few CNPs or uncommon SNVs altering schizophrenia risk, it will represent an important advance in the field. Any CNP association is likely to have immediate biological relevance and amenability to current molecular biology and neuroscience methods. Furthermore, these schizophrenia-associated GWAS loci have never been deeply sequenced in the world-literature. The targeted resequencing data, the imputation reference, and CNP imputation method generated from this R01 will be useful resources for the human genetics community.
StatusActive
Effective start/end date5/15/152/29/20

Funding

  • NIH National Institute of Mental Health (NIMH)

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Schizophrenia
Genome-Wide Association Study
Nucleotides
Mutation
Single Nucleotide Polymorphism
DNA Copy Number Variations
Medical Genetics
Regulator Genes
Neurosciences
Health Expenditures
Molecular Biology
Genome
Morbidity
Costs and Cost Analysis
Mortality