Parisien Marc, Khoury Samar, Chabot-Doré Anne-Julie, Sotocinal Susana G, Slade Gary D, Smith Shad B, Fillingim Roger B, Ohrbach Richard, Greenspan Joel D, Maixner William, Mogil Jeffrey S, Belfer Inna, Diatchenko Luda
Alan Edwards Centre for Research on Pain, McGill University, Montréal, QC H3A 0G4, Canada.
Department of Psychology, McGill University, Montréal, QC H3A 0G4, Canada.
Cell Rep. 2017 May 30;19(9):1940-1952. doi: 10.1016/j.celrep.2017.05.018.
Dorsal root ganglia (DRG) relay sensory information to the brain, giving rise to the perception of pain, disorders of which are prevalent and burdensome. Here, we mapped expression quantitative trait loci (eQTLs) in a collection of human DRGs. DRG eQTLs were enriched within untranslated regions of coding genes of low abundance, with some overlapping with other brain regions and blood cell cis-eQTLs. We confirm functionality of identified eQTLs through their significant enrichment within open chromatin and highly deleterious SNPs, particularly at the exon level, suggesting substantial contribution of eQTLs to alternative splicing regulation. We illustrate pain-related genetic association results explained by DRG eQTLs, with the strongest evidence for contribution of the human leukocyte antigen (HLA) locus, confirmed using a mouse inflammatory pain model. Finally, we show that DRG eQTLs are found among hits in numerous genome-wide association studies, suggesting that this dataset will help address pain components of non-pain disorders.
背根神经节(DRG)将感觉信息传递至大脑,引发疼痛感知,其功能紊乱十分普遍且负担沉重。在此,我们在一组人类DRG中绘制了表达定量性状位点(eQTL)图谱。DRG的eQTL在低丰度编码基因的非翻译区域富集,部分与其他脑区和血细胞顺式eQTL重叠。我们通过在开放染色质和高度有害单核苷酸多态性(SNP)中显著富集,尤其是在外显子水平,证实了所鉴定eQTL的功能,这表明eQTL对可变剪接调控有重要贡献。我们展示了由DRG的eQTL解释的与疼痛相关的遗传关联结果,其中人类白细胞抗原(HLA)位点贡献的证据最为有力,这在小鼠炎性疼痛模型中得到了证实。最后,我们表明在众多全基因组关联研究的结果中发现了DRG的eQTL,这表明该数据集将有助于解决非疼痛性疾病的疼痛成分问题。