Yao Fu, Jennifer A Kelly, Jaanam Gopalakrishnan, Richard C Pelikan, Kandice L Tessneer, Satish Pasula, Kiely Grundahl, David A Murphy, Patrick M Gaffney
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引用次数: 0
摘要
我们在爱泼斯坦-巴氏病毒(Epstein-Barr virus)转化的B细胞系中设计了一种大规模并行报告测定(MPRA),以直接鉴定组蛋白翻译后修饰(即组蛋白定量性状位点(hQTLs)、表达QTLs(eQTLs)以及系统性红斑狼疮和自身免疫(AI)疾病风险单倍型上的变体)以等位基因依赖方式调节调节活性的潜力。我们的研究表明,与其他被测试的变异类别(包括一组先前被证明与 hQTLs 和被测试的 AI 风险变异相互作用的 eQTLs)相比,hQTLs 作为一个群体更有可能在 MPRA 中调节调节活性。此外,我们还提名了 17 个变异(包括 11 个以前未报道的变异)为系统性红斑狼疮的假定致病变异,另外 14 个为其他各种 AI 疾病的假定致病变异,并将这些变异列为未来在原代和永生 B 细胞中进行功能研究的优先对象。因此,我们揭示了系统性红斑狼疮和人工智能疾病表型中基因型、表观遗传学和基因表达之间的机理关系。
Massively parallel reporter assay confirms regulatory potential of hQTLs and reveals important variants in lupus and other autoimmune diseases.
We designed a massively parallel reporter assay (MPRA) in an Epstein-Barr virus transformed B cell line to directly characterize the potential for histone post-translational modifications, i.e., histone quantitative trait loci (hQTLs), expression QTLs (eQTLs), and variants on systemic lupus erythematosus (SLE) and autoimmune (AI) disease risk haplotypes to modulate regulatory activity in an allele-dependent manner. Our study demonstrates that hQTLs, as a group, are more likely to modulate regulatory activity in an MPRA compared with other variant classes tested, including a set of eQTLs previously shown to interact with hQTLs and tested AI risk variants. In addition, we nominate 17 variants (including 11 previously unreported) as putative causal variants for SLE and another 14 for various other AI diseases, prioritizing these variants for future functional studies in primary and immortalized B cells. Thus, we uncover important insights into the mechanistic relationships among genotype, epigenetics, and gene expression in SLE and AI disease phenotypes.