Kirsten Holger, Al-Hasani Hoor, Holdt Lesca, Gross Arnd, Beutner Frank, Krohn Knut, Horn Katrin, Ahnert Peter, Burkhardt Ralph, Reiche Kristin, Hackermüller Jörg, Löffler Markus, Teupser Daniel, Thiery Joachim, Scholz Markus
Institute for Medical Informatics, Statistics and Epidemiology, LIFE - Leipzig Research Center for Civilization Diseases, Cognitive Genetics, Department of Cell Therapy.
Department for Computer Science, Analysis Strategies Group, Department of Diagnostics, Young Investigators Group Bioinformatics and Transcriptomics, Department Proteomics, Helmholtz Centre for Environmental Research - UFZ, Leipzig, Germany and.
Hum Mol Genet. 2015 Aug 15;24(16):4746-63. doi: 10.1093/hmg/ddv194. Epub 2015 May 27.
Genetics of gene expression (eQTLs or expression QTLs) has proved an indispensable tool for understanding biological pathways and pathomechanisms of trait-associated SNPs. However, power of most genome-wide eQTL studies is still limited. We performed a large eQTL study in peripheral blood mononuclear cells of 2112 individuals increasing the power to detect trans-effects genome-wide. Going beyond univariate SNP-transcript associations, we analyse relations of eQTLs to biological pathways, polygenetic effects of expression regulation, trans-clusters and enrichment of co-localized functional elements. We found eQTLs for about 85% of analysed genes, and 18% of genes were trans-regulated. Local eSNPs were enriched up to a distance of 5 Mb to the transcript challenging typically implemented ranges of cis-regulations. Pathway enrichment within regulated genes of GWAS-related eSNPs supported functional relevance of identified eQTLs. We demonstrate that nearest genes of GWAS-SNPs might frequently be misleading functional candidates. We identified novel trans-clusters of potential functional relevance for GWAS-SNPs of several phenotypes including obesity-related traits, HDL-cholesterol levels and haematological phenotypes. We used chromatin immunoprecipitation data for demonstrating biological effects. Yet, we show for strongly heritable transcripts that still little trans-chromosomal heritability is explained by all identified trans-eSNPs; however, our data suggest that most cis-heritability of these transcripts seems explained. Dissection of co-localized functional elements indicated a prominent role of SNPs in loci of pseudogenes and non-coding RNAs for the regulation of coding genes. In summary, our study substantially increases the catalogue of human eQTLs and improves our understanding of the complex genetic regulation of gene expression, pathways and disease-related processes.
基因表达遗传学(eQTL,即表达数量性状基因座)已被证明是理解性状相关单核苷酸多态性(SNP)的生物学途径和发病机制的不可或缺的工具。然而,大多数全基因组eQTL研究的效能仍然有限。我们对2112名个体的外周血单核细胞进行了一项大型eQTL研究,提高了全基因组检测反式效应的效能。除了单变量SNP-转录本关联分析,我们还分析了eQTL与生物学途径的关系、表达调控的多基因效应、反式簇以及共定位功能元件的富集情况。我们发现约85%的分析基因存在eQTL,18%的基因受到反式调控。局部eSNP在距离转录本5 Mb范围内富集,这对通常实施的顺式调控范围提出了挑战。GWAS相关eSNP调控基因内的通路富集支持了所鉴定eQTL的功能相关性。我们证明GWAS-SNP的最邻近基因可能常常是误导性的功能候选基因。我们鉴定出了与包括肥胖相关性状、高密度脂蛋白胆固醇水平和血液学表型在内的几种表型的GWAS-SNP具有潜在功能相关性的新型反式簇。我们使用染色质免疫沉淀数据来证明生物学效应。然而,我们发现对于强遗传力的转录本,所有鉴定出的反式eSNP所解释的反式染色体遗传力仍然很少;不过,我们的数据表明这些转录本的大多数顺式遗传力似乎是可以解释的。对共定位功能元件的剖析表明,SNP在假基因和非编码RNA基因座中对编码基因的调控起着重要作用。总之,我们的研究大幅增加了人类eQTL的目录,并增进了我们对基因表达、途径和疾病相关过程的复杂遗传调控的理解。