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Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue

机译:正常脑组织中与精神分裂症和情感障碍相关的表达数量性状基因座的鉴定

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摘要

Schizophrenia and the affective disorders, here comprising bipolar disorder and major depressive disorder, are psychiatric illnesses that lead to significant morbidity and mortality worldwide. Whilst understanding of their pathobiology remains limited, large case-control studies have recently identified single nucleotide polymorphisms (SNPs) associated with these disorders. However, discerning the functional effects of these SNPs has been difficult as the associated causal genes are unknown. Here we evaluated whether schizophrenia and affective disorder associated-SNPs are correlated with gene expression within human brain tissue. Specifically, to identify expression quantitative trait loci (eQTLs), we leveraged disorder-associated SNPs identified from 11 genome-wide association studies with gene expression levels in post-mortem, neurologically-normal tissue from two independent human brain tissue expression datasets (UK Brain Expression Consortium (UKBEC) and Genotype-Tissue Expression (GTEx)). Utilizing stringent multi-region meta-analyses, we identified 2,224 cis-eQTLs associated with expression of 40 genes, including 11 non-coding RNAs. One cis-eQTL, rs16969968, results in a functionally disruptive missense mutation in CHRNA5, a schizophrenia-implicated gene. Importantly, comparing across tissues, we find that blood eQTLs capture < 10% of brain cis-eQTLs. Contrastingly, > 30% of brain-associated eQTLs are significant in tibial nerve. This study identifies putatively causal genes whose expression in region-specific tissue may contribute to the risk of schizophrenia and affective disorders.
机译:精神分裂症和情感障碍,这里包括躁郁症和重度抑郁症,是精神病,导致全世界范围内高发病率和高死亡率。尽管对其病理生物学的了解仍然有限,但大型病例对照研究最近发现了与这些疾病相关的单核苷酸多态性(SNP)。然而,由于相关的致病基因是未知的,因此很难识别这些SNP的功能作用。在这里,我们评估了精神分裂症和与情感障碍相关的SNP是否与人脑组织内的基因表达相关。具体而言,为了鉴定表达定量特征位点(eQTL),我们利用了从11个全基因组关联研究中鉴定的与疾病相关的SNP,以及来自两个独立的人脑组织表达数据集(英国脑组织)的验尸,神经系统正常组织中的基因表达水平。表达协会(UKBEC)和基因型组织表达(GTEx))。利用严格的多区域荟萃分析,我们鉴定了2,224个与40个基因的表达相关的顺式eQTL,其中包括11个非编码RNA。一个顺式eQTL rs16969968在精神分裂症相关基因CHRNA5中导致功能破坏性错义突变。重要的是,通过比较不同组织,我们发现血液eQTL捕获的脑顺式eQTL小于10%。相反,在胫骨神经中,有超过30%的与大脑相关的eQTL很重要。这项研究确定了可能的致病基因,其在特定区域组织中的表达可能会导致精神分裂症和情感障碍。

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