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本文引用的文献

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Int J Mol Sci. 2021 Dec 28;23(1):288. doi: 10.3390/ijms23010288.
2
The UCSC Genome Browser database: 2022 update.UCSC 基因组浏览器数据库:2022 年更新。
Nucleic Acids Res. 2022 Jan 7;50(D1):D1115-D1122. doi: 10.1093/nar/gkab959.
3
Inflammatory bowel disease: between genetics and microbiota.炎症性肠病:遗传与微生物组之间。
Mol Biol Rep. 2020 Apr;47(4):3053-3063. doi: 10.1007/s11033-020-05318-5. Epub 2020 Feb 21.
4
Increased Risk of Inflammatory Bowel Disease in Families with Tonsillectomy: A Danish National Cohort Study.扁桃体切除术家族中炎症性肠病风险增加:一项丹麦全国队列研究。
Epidemiology. 2019 Mar;30(2):256-262. doi: 10.1097/EDE.0000000000000946.
5
The Environmental Sensor AHR Protects from Inflammatory Damage by Maintaining Intestinal Stem Cell Homeostasis and Barrier Integrity.环境传感器 AHR 通过维持肠道干细胞稳态和屏障完整性来防止炎症损伤。
Immunity. 2018 Aug 21;49(2):353-362.e5. doi: 10.1016/j.immuni.2018.07.010. Epub 2018 Aug 14.
6
Genetic Markers Predict Primary Nonresponse and Durable Response to Anti-Tumor Necrosis Factor Therapy in Ulcerative Colitis.遗传标志物可预测溃疡性结肠炎患者对抗肿瘤坏死因子治疗的原发性无应答和持久应答。
Inflamm Bowel Dis. 2018 Jul 12;24(8):1840-1848. doi: 10.1093/ibd/izy083.
7
Aryl hydrocarbon receptor and intestinal immunity.芳烃受体与肠道免疫。
Mucosal Immunol. 2018 Jul;11(4):1024-1038. doi: 10.1038/s41385-018-0019-2. Epub 2018 Apr 7.
8
Identification and Functional Analysis of Gene Regulatory Sequences Interacting with Colorectal Tumor Suppressors.与结直肠癌肿瘤抑制因子相互作用的基因调控序列的鉴定与功能分析
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9
NOD2 and inflammation: current insights.NOD2与炎症:当前见解
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10
Familial and ethnic risk in inflammatory bowel disease.炎症性肠病中的家族和种族风险。
Ann Gastroenterol. 2018 Jan-Feb;31(1):14-23. doi: 10.20524/aog.2017.0208. Epub 2017 Oct 26.

一个溃疡性结肠炎的家系定位于 7p21.1,该区域包含一个芳烃受体基因的调控活性区域。

A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor gene.

机构信息

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.

出版信息

Eur J Hum Genet. 2023 Dec;31(12):1440-1446. doi: 10.1038/s41431-023-01298-9. Epub 2023 Feb 3.

DOI:10.1038/s41431-023-01298-9
PMID:36732664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10689720/
Abstract

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.

摘要

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。