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研究南非人群中染色体 17 候选基因对结核病易感性的影响。

Investigation of chromosome 17 candidate genes in susceptibility to TB in a South African population.

机构信息

Molecular Biology and Human Genetics, MRC Centre for Molecular and Cellular Biology and the DST/NRF Centre of Excellence for Biomedical TB Research, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa.

出版信息

Tuberculosis (Edinb). 2009 Mar;89(2):189-94. doi: 10.1016/j.tube.2008.10.001. Epub 2009 Jan 14.

Abstract

Chromosome 17 is known to contain TB susceptibility genes. Polymorphisms in two of these genes, namely NOS2A and CCL2, have been associated with TB in various populations. To investigate a possible association of gene variants with TB in the South African Coloured population we genotyped SNPs from NOS2A and CCL2 in over 800 TB cases and controls. We found a significant association between TB and two haplotypes, containing the functional rs9282799 and rs8078340 SNPs, in the NOS2A promoter. The T allele of rs8078340, found in the haplotype over-represented in cases (p=0.015, p(c)=0.038, OR=1.4, 95% CI [1.1-1.8]), was previously shown to decrease the quantity of DNA-protein complex bound as well as the duration of binding and may decrease nitric oxide (NO) production. The C allele of rs8078340 was present in the haplotype more frequent in controls (p=0.011, p(c)=0.029, OR=1.4, 95% CI [1.1-1.8]). In the single-point analysis of NOS2A, rs2779249 (previously associated with TB in Brazilians) and the functional rs8078340 were nominally associated with disease. No association was found between any of the other SNPs or haplotypes studied and TB. This study presents evidence that haplotypes in the NOS2A promoter influence susceptibility to TB and confirms the importance of NO production in the disease.

摘要

17 号染色体已知包含结核易感性基因。这些基因中的两个基因,即 NOS2A 和 CCL2 的多态性与各种人群中的结核病有关。为了研究基因变异与南非有色人种结核病之间的可能关联,我们对超过 800 例结核病病例和对照者的 NOS2A 和 CCL2 中的 SNP 进行了基因分型。我们发现,NOS2A 启动子中包含功能性 rs9282799 和 rs8078340 SNP 的两个单倍型与结核病之间存在显著关联。在病例中过度表达的单倍型中发现了 rs8078340 的 T 等位基因(p=0.015,p(c)=0.038,OR=1.4,95%CI[1.1-1.8]),先前的研究表明,该等位基因降低了 DNA-蛋白质复合物的结合量和结合持续时间,可能会降低一氧化氮(NO)的产生。rs8078340 的 C 等位基因在对照组中更为常见的单倍型中存在(p=0.011,p(c)=0.029,OR=1.4,95%CI[1.1-1.8])。在 NOS2A 的单点分析中,rs2779249(先前与巴西人的结核病有关)和功能性 rs8078340 与疾病具有名义关联。未发现研究中的其他 SNP 或单倍型与结核病之间存在关联。这项研究提供了证据表明,NOS2A 启动子中的单倍型影响结核病的易感性,并证实了一氧化氮产生在疾病中的重要性。

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