35 - OVEREXPRESSION OF MULTIPLE TRANSCRIPTS OF SNX19 (SORTING NEXIN 19) IN MULTIPLE BRAIN REGIONS MAY CONTRIBUTE TO SCHIZOPHRENIA RISK

Abstract

Background Genome-Wide Association Studies (GWAS) have identified many genomic loci associated with risk for schizophrenia, but unambiguous identification of specific risk genes has proved difficult. We investigated the 2 megabase genomic region flanking index SNP rs10791097, the 16th ranked SNP in the 2014 publication from the Psychiatric Genomics Consortium (PGC) GWAS for schizophrenia. Methods We performed RNA sequencing (RNAseq) on samples from human postmortem DLPFC, hippocampus, and caudate from the Lieber Institute Human Brain Repository (N=~495, of which 175 were patients diagnosed with schizophrenia). To detect expression quantitative trait loci (eQTLs), we tested for association between genotypes at regional GWAS schizophrenia risk variants and expressed features at the gene, exon, and junction levels under a simple additive genetic model. Results Dozens of PGC GWAS-significant markers in the region were strongly associated with expressed features in SNX19, with eQTL p values ranging from 3.06E-07 to 1.58E-44. In contrast, eleven other genes in the region produced much weaker results. A junction between exons 8 and 9 defined a canonical class of “full length” SNX19 transcripts (junc8.9 at hg19 position chr11:130750702-130773149) which was only weakly associated with genetic risk. In contrast, the PGC index SNP rs10791097 was associated with expression of a rarer class of transcripts, defined by a junction between exons 8 and 10 (junc8.10, chr11:130749607-130773149), in DLPFC (eQTL p= 5.98E-26), hippocampus (p=1.04E-19), and caudate (p=6.87E-19), with the clinical risk allele (T) predicting greater expression. Many of the junc8.10 eQTLs were confirmed in both GTEx (multiple brain regions) and in the CommonMind Consortium (DLPFC) datasets. Of note, only 46% of the 495 postmortem DLPFC samples had junc8.10 read counts > 0. Discussion In addition, we found highly significant eQTLs across multiple brain regions involving 4 other expressed features: 1) a novel junction at position chr11:130765052-130773149, 2) a novel junction at chr11:130750702-130764497), 3) a known exon at chr11:130762646-130762954, and 4) a known exon at chr11:130763659-130763769. These 4 features defined 4 more independent classes of transcripts, each with the clinical risk alleles predicting greater expression. Across 3 different brain regions, PGC GWAS risk genotypes were associated with expression levels of 5 classes of SNX19 protein coding transcripts. We suggest that a critical element of the molecular mechanism(s) of schizophrenia risk from this GWAS locus is likely to be over-expression in multiple brain regions of multiple SNX19 transcripts and proteins of diverse structure and function.