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鉴定与结核病相关的新型 IRGM 启动子单核苷酸多态性。

Identification of a novel IRGM promoter single nucleotide polymorphism associated with tuberculosis.

机构信息

Department of Bacteriology and Immunology, Beijing Tuberculosis & Thoracic Tumor Research Institute, Tongzhou District, Beijing 101149, PR China.

出版信息

Clin Chim Acta. 2010 Nov 11;411(21-22):1645-9. doi: 10.1016/j.cca.2010.06.009. Epub 2010 Jun 11.

Abstract

BACKGROUND

Human immunity-related GTPase M (IRGM) is found to play an important role in defense against intracellular pathogen Mycobacterium tuberculosis in vitro by regulating autophagy. To verify whether single nucleotide polymorphisms (SNPs) in the promoter region of IRGM gene are associated with tuberculosis (TB) 1.7 kb IRGM promoter region was sequenced and SNP analysis was conducted in TB patients and healthy controls.

METHODS

A simple and rapid procedure for extracting DNA from clotted-blood was developed in this study. A 1.7 kb IRGM promoter region was amplified and sequenced for nucleotide polymorphism search. Then, 3 SNPs were selected and analyzed in 216TB patients and 275 healthy subjects by ligase detection reaction technique.

RESULTS

DNA extracted by our method was of high quality and suitable for PCR, sequencing, and genotyping. We identified 29 polymorphisms in the 1.7 kb IRGM promoter region, including 11 novel polymorphisms not yet reported. Large population analysis showed that frequencies of -1208A allele (P=0.031), -1208AA genotype (P=0.042), and -1208A/-1161C/-947C (P=0.035) and -1208G/-1161C/-947C (P=0.030) haplotypes in cases were significantly different from those in controls.

CONCLUSIONS

In 1.7 kb IRGM promoter region, only -1208A/G polymorphism is associated with susceptibility to TB.

摘要

背景

人类免疫相关 GTP 酶 M(IRGM)在体外通过调节自噬来发挥重要作用,抵抗细胞内病原体结核分枝杆菌。为了验证 IRGM 基因启动子区域中的单核苷酸多态性(SNP)是否与结核病(TB)相关,我们对 TB 患者和健康对照者进行了 1.7 kb IRGM 启动子区域的测序和 SNP 分析。

方法

本研究建立了一种从凝血血液中提取 DNA 的简单、快速方法。扩增并测序 1.7 kb 的 IRGM 启动子区域,以寻找核苷酸多态性。然后,采用连接酶检测反应技术在 216 例 TB 患者和 275 例健康对照者中分析了 3 个 SNP。

结果

我们的方法提取的 DNA 质量高,适用于 PCR、测序和基因分型。我们在 1.7 kb 的 IRGM 启动子区域中鉴定出 29 个多态性,包括 11 个尚未报道的新多态性。大规模人群分析显示,-1208A 等位基因(P=0.031)、-1208AA 基因型(P=0.042)、-1208A/-1161C/-947C(P=0.035)和-1208G/-1161C/-947C(P=0.030)单倍型在病例组中的频率明显低于对照组。

结论

在 1.7 kb 的 IRGM 启动子区域中,只有-1208A/G 多态性与 TB 的易感性相关。

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