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Polymorphic allele of human MRC1 confer protection against tuberculosis in a Chinese population

机译:人类MRC1的多态性等位基因赋予中国人群预防结核病的能力

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Mannose receptor is a member of the C-type lectin receptor family involved in pathogen molecular-pattern recognition and plays a critical role in shaping host immune response. Single nucleotide polymorphisms (SNPs) in the MRC1 gene may affect expression levels and differences in the structure and function of proteins in different individuals thereby affecting individual susceptibility to pulmonary tuberculosis. However to date MRC1 polymorphisms associated with susceptibility to pulmonary tuberculosis have not yet been reported. The present study aimed to investigate potential associations of SNPs in the MRC1 gene with pulmonary tuberculosis in a Chinese population. Six SNPs (G1186A G1195A T1212C C1221G C1303T and C1323T) in exon 7 of the MRC1 gene were genotyped using the PCR and DNA sequencing methods in the pulmonary tuberculosis patients and the healthy controls. Linkage disequilibrium analysis was performed between polymorphic sites. The study found that the allele frequency of G1186A (rs34039386) of the MRC1 gene in a Chinese population was higher in the pulmonary tuberculosis group than the healthy control group. There was a significant difference in frequency distribution between the two groups (P = 0.037; OR = 0.76; 95% CI 0.58-0.98). Genotypic analysis also indicated that the AG genotypes in a Chinese population were significantly correlated with pulmonary tuberculosis (P < 0.01; OR = 0.57; 95% CI 0.37-0.87). After adjustment for age and gender G1186A sites were found to be dominant (P < 0.01; OR = 0.59; 95% CI 0.40-0.87) over-dominant (P = 0.045; OR = 0.69; 95% CI 0.47-0.99) and additive models (P = 0.041; OR = 0.76; 95% CI 0.59-0.99) in association with pulmonary tuberculosis. But no association was found between the other 5 SNPs (G1195A, T1212C, C1221G, C1303T and C1323T) and tuberculosis (P > 0.05). This study is the first to report that genetic variants in the MRC1 gene can be associated with pulmonary tuberculosis in a Chinese population, and may reduce the risk of infecting pulmonary tuberculosis. This also provides a new experimental basis to clarify the pathogenesis of pulmonary tuberculosis.
机译:甘露糖受体是参与病原体分子模式识别的C型凝集素受体家族的成员,在塑造宿主免疫应答中起关键作用。 MRC1基因中的单核苷酸多态性(SNP)可能会影响不同个体的表达水平以及蛋白质结构和功能的差异,从而影响个体对肺结核的易感性。然而,迄今为止,尚未报道与肺结核易感性相关的MRC1多态性。本研究旨在调查中国人群中MRC1基因中SNP与肺结核的潜在关联。使用PCR和DNA测序方法对肺结核患者和健康对照组的MRC1基因第7外显子中的六个SNP(G1186A G1195A T1212C C1221G C1303T和C1323T)进行基因分型。在多态性位点之间进行连锁不平衡分析。研究发现,肺结核组中中国人群中MRC1基因G1186A(rs34039386)的等位基因频率高于健康对照组。两组之间的频率分布存在显着差异(P = 0.037; OR = 0.76; 95%CI 0.58-0.98)。基因型分析还表明,中国人群中AG基因型与肺结核显着相关(P <0.01; OR = 0.57; 95%CI 0.37-0.87)。调整年龄和性别后,发现G1186A位点占优势(P <0.01; OR = 0.59; 95%CI 0.40-0.87)高于优势(P = 0.045; OR = 0.69; 95%CI 0.47-0.99)与肺结核相关的模型(P = 0.041; OR = 0.76; 95%CI 0.59-0.99)。但在其他5个SNP(G1195A,T1212C,C1221G,C1303T和C1323T)与结核之间未发现关联(P> 0.05)。这项研究是第一个报告说MRC1基因的遗传变异可能与中国人群的肺结核有关,并可能降低感染肺结核的风险。这也为阐明肺结核的发病机理提供了新的实验基础。

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