Characterization of a REST-Regulated Internal Promoter in the Schizophrenia Genome-Wide Associated Gene MIR137

• Published in: Schizophrenia bulletin Vol. 41; no. 3; pp. 698 - 707
• Main Authors: Warburton, Alix, Breen, Gerome, Rujescu, Dan, Bubb, Vivien J, Quinn, John P
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.05.2015
• Subjects: Cell Line, Tumor; Gene Expression - genetics; Gene-Environment Interaction; Genome-Wide Association Study; Humans; MicroRNAs - genetics; Minisatellite Repeats - genetics; Promoter Regions, Genetic - genetics; Regular; Repressor Proteins - genetics; Response Elements - genetics; Schizophrenia - genetics; variable number tandem repeat; gene environment interaction; microRNA-137; cocaine
• ISSN: 0586-7614; 1745-1701
• DOI: 10.1093/schbul/sbu117

MIR137 has been identified as a candidate gene for schizophrenia from genome-wide association studies via association with an intronic single nucleotide polymorphism (SNP), rs1625579. The location of the SNP suggests one mechanism in which transcriptional or posttranscriptional regulation of miR-137 expression could underlie schizophrenia. We identified and validated a novel promoter of the MIR137 gene adjacent to miR-137 itself which can direct the expression of distinct mRNA isoforms encoding miR-137. Analysis of both endogenous gene expression and reporter gene assays determined that this internal promoter is regulated by repressor element-1 silencing transcription factor (REST), which has previously been associated with pathways linked to schizophrenia. Distinct isoforms of REST mediate differential expression at this locus, suggesting the relative levels of these isoforms are important for miR-137 expression profiles. The internal promoter contains a variable number tandem repeat (VNTR) domain adjacent to the pre-miR-137 sequence. The reporter gene activity directed by this promoter was modified by the genotype of the VNTR. Differential expression was also observed in response to cocaine, which is known to regulate the REST pathway in SH-SY5Y cells. Our data support the hypothesis that a "gene × environment" interaction could modify the level of miR-137 expression via this internal promoter and that the genotype of the VNTR could modulate transcriptional responses. We demonstrate that this promoter region is not in disequilibrium with rs1625579 and therefore would supply a distinct pathway to potentially alter miR-137 levels in response to environmental cues.