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Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

机译:基于途径的整合方法可确定CTCF和CACNB2基因组区域与精神分裂症之间的关联

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摘要

In the present study, an integrated hierarchical approach was applied to: (1) identify pathways associated with susceptibility to schizophrenia; (2) detect genes that may be potentially affected in these pathways since they contain an associated polymorphism; and (3) annotate the functional consequences of such single-nucleotide polymorphisms (SNPs) in the affected genes or their regulatory regions. The Global Test was applied to detect schizophrenia-associated pathways using discovery and replication datasets comprising 5,040 and 5,082 individuals of European ancestry, respectively. Information concerning functional gene-sets was retrieved from the Kyoto Encyclopedia of Genes and Genomes, Gene Ontology, and the Molecular Signatures Database. Fourteen of the gene-sets or pathways identified in the discovery dataset were confirmed in the replication dataset. These include functional processes involved in transcriptional regulation and gene expression, synapse organization, cell adhesion, and apoptosis. For two genes, i.e. CTCF and CACNB2, evidence for association with schizophrenia was available (at the gene-level) in both the discovery study and published data from the Psychiatric Genomics Consortium schizophrenia study. Furthermore, these genes mapped to four of the 14 presently identified pathways. Several of the SNPs assigned to CTCF and CACNB2 have potential functional consequences, and a gene in close proximity to CACNB2, i.e. ARL5B, was identified as a potential gene of interest. Application of the present hierarchical approach thus allowed: (1) identification of novel biological gene-sets or pathways with potential involvement in the etiology of schizophrenia, as well as replication of these findings in an independent cohort; (2) detection of genes of interest for future follow-up studies; and (3) the highlighting of novel genes in previously reported candidate regions for schizophrenia.
机译:在本研究中,一种集成的分层方法应用于:(1)识别与精神分裂症易感性相关的途径; (2)检测可能在这些途径中受到影响的基因,因为它们含有相关的多态性; (3)注释此类单核苷酸多态性(SNP)在受影响的基因或其调控区域中的功能后果。使用包含分别来自欧洲血统的5,040和5,082个个体的发现和复制数据集,将全球测试应用于检测精神分裂症相关的途径。有关功能基因集的信息可从《京都基因与基因组百科全书》,《基因本体论》和《分子标记数据库》中检索。在复制数据集中确认了发现数据集中确定的14个基因集或途径。这些包括参与转录调节和基因表达,突触组织,细胞粘附和细胞凋亡的功能过程。对于两个基因,即CTCF和CACNB2,在发现研究和Psychiatric Genomics Consortium精神分裂症研究中都可获得与精神分裂症相关的证据(在基因水平上)。此外,这些基因定位到目前鉴定的14种途径中的4种。分配给CTCF和CACNB2的多个SNP具有潜在的功能后果,并且已将与CACNB2紧密相关的基因(即ARL5B)鉴定为潜在的目标基因。因此,本分级方法的应用使得:(1)鉴定出可能与精神分裂症的病因有关的新的生物学基因集或途径,并在一个独立的队列中复制这些发现; (2)检测感兴趣的基因,以供将来的后续研究; (3)在先前报道的精神分裂症候选区域中突出新基因。

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