RCLINK, Department of Cellular and Molecular Medicine, Panum Institute, University of Copenhagen, Blegdamsvej 3, DK-2200, Copenhagen N, Denmark.
Department of Science and Environment, Roskilde University, Roskilde, Denmark.
Eur J Hum Genet. 2023 Dec;31(12):1440-1446. doi: 10.1038/s41431-023-01298-9. Epub 2023 Feb 3.
We have mapped a locus on chromosome 7p22.3-7p15.3 spanning a 22.4 Mb region for ulcerative colitis (UC) by whole genome linkage analyses of a large Danish family. The family represent three generations with UC segregating as an autosomal dominant trait with variable expressivity. The whole-genome scan resulted in a logarithm of odds score (LOD score) of Z = 3.31, and a whole genome sequencing (WGS) of two affected excluded disease-causing mutations in the protein coding genes. Two rare heterozygote variants, rs182281985:G>A and rs541426369:G>A, both with low allele frequencies (MAF A:0.0001, gnomAD ver3.1.2), were found in clusters of ChiP-seq transcription factors binding sites close to the AHR (aryl hydrocarbon receptor) gene and the UC associated SNP rs1077773:G>A. Testing the two SNPs in a promoter reporter assay for regulatory activity revealed that rs182281985:G>A influenced the AHR promoter. These results suggest a regulatory region that include rs182281985:G>A close to the UC GWAS SNP rs1077773:G>A and further demonstrate evidence that the AHR gene on the 7p-tel region is a candidate susceptible gene for UC.
我们通过对一个丹麦大家庭的全基因组连锁分析,在染色体 7p22.3-7p15.3 上定位了一个与溃疡性结肠炎 (UC) 相关的基因座,跨度为 22.4Mb。该家系代表了三代人,UC 作为一种常染色体显性遗传疾病,具有不同的外显率。全基因组扫描得到的对数优势分数 (LOD 分数) 为 Z=3.31,对两个受影响的个体进行全基因组测序 (WGS) 排除了蛋白质编码基因中的致病突变。两个罕见的杂合变体,rs182281985:G>A 和 rs541426369:G>A,均具有较低的等位基因频率 (MAF A:0.0001,gnomAD ver3.1.2),在 ChiP-seq 转录因子结合位点的簇中被发现,靠近 AHR(芳香烃受体)基因和与 UC 相关的 SNP rs1077773:G>A。在启动子报告基因检测中检测这两个 SNP 的调控活性表明,rs182281985:G>A 影响 AHR 启动子。这些结果表明,一个包含 rs182281985:G>A 的调控区域,靠近 UC GWAS SNP rs1077773:G>A,并进一步证明了 7p 端区域的 AHR 基因是 UC 的候选易感基因。