Abstract:
BACKGROUND:Genetic studies of schizophrenia have implicated numerous risk loci including several copy number variants (CNVs) of large effect and hundreds of loci of small effect. In only a few cases has a specific gene been clearly identified. Rare CNVs affecting a single gene offer a potential avenue to discovering schizophrenia risk genes. METHODS:CNVs were generated from exome sequencing of 4913 schizophrenia cases and 6188 control subjects from Sweden. We integrated two CNV calling methods (XHMM and ExomeDepth) to expand our set of single-gene CNVs and leveraged two different approaches for validating these variants (quantitative polymerase chain reaction and NanoString). RESULTS:We found a significant excess of all rare CNVs (deletions: p = .0004, duplications: p = .0006) and single-gene CNVs (deletions: p = .04, duplications: p = .03) in schizophrenia cases compared with control subjects. An expanded set of CNVs generated from integrating multiple approaches showed a significant burden of deletions in 11 of 21 gene sets previously implicated in schizophrenia and across all genes in those sets (p = .008), although no tests survived correction. We performed an extensive validation of all deletions in the significant set of voltage-gated calcium channels among CNVs called from both exome sequencing and genotyping arrays. In total, 4 exonic, single-gene deletions were validated in schizophrenia cases and none in control subjects (p = .039), of which all were identified by exome sequencing. CONCLUSIONS:These results point to the potential contribution of single-gene CNVs to schizophrenia, indicate that the utility of exome sequencing for CNV calling has yet to be maximized, and note that single-gene CNVs should be included in gene-focused studies using other classes of variation.
journal_name
Biol Psychiatryjournal_title
Biological psychiatryauthors
Szatkiewicz JP,Fromer M,Nonneman RJ,Ancalade N,Johnson JS,Stahl EA,Rees E,Bergen SE,Hultman CM,Kirov G,O'Donovan M,Owen M,Holmans P,Sklar P,Sullivan PF,Purcell SM,Crowley JJ,Ruderfer DMdoi
10.1016/j.biopsych.2019.09.023subject
Has Abstractpub_date
2020-04-15 00:00:00pages
736-744issue
8eissn
0006-3223issn
1873-2402pii
S0006-3223(19)31748-2journal_volume
87pub_type
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