Lin Jhih-Rong, Cai Ying, Zhang Quanwei, Zhang Wen, Nogales-Cadenas Rubén, Zhang Zhengdong D
Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.
Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461
Genetics. 2016 Dec;204(4):1587-1600. doi: 10.1534/genetics.116.187195. Epub 2016 Oct 17.
Schizophrenia is a severe mental disorder with a large genetic component. Recent genome-wide association studies (GWAS) have identified many schizophrenia-associated common variants. For most of the reported associations, however, the underlying biological mechanisms are not clear. The critical first step for their elucidation is to identify the most likely disease genes as the source of the association signals. Here, we describe a general computational framework of post-GWAS analysis for complex disease gene prioritization. We identify 132 putative schizophrenia risk genes in 76 risk regions spanning 120 schizophrenia-associated common variants, 78 of which have not been recognized as schizophrenia disease genes by previous GWAS. Even more significantly, 29 of them are outside the risk regions, likely under regulation of transcriptional regulatory elements contained therein. These putative schizophrenia risk genes are transcriptionally active in both brain and the immune system, and highly enriched among cellular pathways, consistent with leading pathophysiological hypotheses about the pathogenesis of schizophrenia. With their involvement in distinct biological processes, these putative schizophrenia risk genes, with different association strengths, show distinctive temporal expression patterns, and play specific biological roles during brain development.
精神分裂症是一种具有很大遗传成分的严重精神障碍。最近的全基因组关联研究(GWAS)已经鉴定出许多与精神分裂症相关的常见变异。然而,对于大多数已报道的关联,其潜在的生物学机制尚不清楚。阐明这些机制的关键第一步是确定最有可能的疾病基因作为关联信号的来源。在此,我们描述了一种用于复杂疾病基因优先级排序的GWAS后分析的通用计算框架。我们在跨越120个与精神分裂症相关的常见变异的76个风险区域中鉴定出132个推定的精神分裂症风险基因,其中78个基因以前的GWAS未将其识别为精神分裂症疾病基因。更重要的是,其中29个基因在风险区域之外,可能受其中所含转录调控元件的调控。这些推定的精神分裂症风险基因在大脑和免疫系统中均具有转录活性,并且在细胞途径中高度富集,这与关于精神分裂症发病机制的主要病理生理假设一致。由于它们参与不同的生物学过程,这些具有不同关联强度的推定精神分裂症风险基因表现出独特的时间表达模式,并在大脑发育过程中发挥特定的生物学作用。