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澳大利亚原住民的细胞因子基因多态性。

Cytokine gene polymorphism among Indigenous Australians.

作者信息

Cox Amanda J, Moscovis Sophia M, Blackwell C Caroline, Scott Rodney J

机构信息

1Faculty of Health, University of Newcastle, Newcastle, NSW, Australia.

出版信息

Innate Immun. 2014 May;20(4):431-9. doi: 10.1177/1753425913498911. Epub 2013 Aug 12.

DOI:10.1177/1753425913498911
PMID:23940076
Abstract

The health profile of Indigenous Australians is characterised by high rates of classic 'lifestyle' diseases. Potential roles of inflammation in pathophysiology of these diseases requires investigation. It is not clear if genetic regulation of inflammation in Indigenous Australians is similar to other populations. This study characterised frequencies of single nucleotide polymorphisms (SNPs) for eight cytokine genes for 100 individuals from a remote Indigenous Australian community and assessed novel genetic variants in four cytokine genes. We used a commercially-available allelic discrimination assay for SNP genotyping; re-sequencing was undertaken by standard Sanger sequencing methodologies for 26 samples. Frequencies of cytokine gene SNPs differed significantly from the Caucasian population (P < 0.001-0.044). Twenty-five novel variants were identified across four re-sequenced genes; frequencies ranged from <5% to 100%. Genotype frequencies observed in Indigenous Australians did not consistently resemble reported HapMap frequencies in Northern and Western European populations, Yoruba Nigerian or Han Chinese. Our findings indicate Indigenous Australians might have an inherited propensity for strong inflammatory responses. Preliminary evidence of novel genetic variants highlights the need to catalogue the extent of genetic variation in specific population groups. Improved understanding of differences in genetic variation between specific population groups could assist in assessment of risk for lifestyle diseases.

摘要

澳大利亚原住民的健康状况以典型“生活方式”疾病的高发病率为特征。炎症在这些疾病病理生理学中的潜在作用需要进行研究。目前尚不清楚澳大利亚原住民炎症的基因调控是否与其他人群相似。本研究对来自澳大利亚偏远原住民社区的100名个体的8种细胞因子基因的单核苷酸多态性(SNP)频率进行了特征分析,并评估了4种细胞因子基因中的新型遗传变异。我们使用市售的等位基因鉴别分析进行SNP基因分型;对26个样本采用标准桑格测序方法进行重测序。细胞因子基因SNP的频率与白种人群有显著差异(P < 0.001 - 0.044)。在4个重测序基因中鉴定出25个新型变异;频率范围从<5%到100%。在澳大利亚原住民中观察到的基因型频率并不总是与北欧和西欧人群、约鲁巴尼日利亚人或汉族人群中报道的HapMap频率相似。我们的研究结果表明,澳大利亚原住民可能具有强烈炎症反应的遗传倾向。新型遗传变异的初步证据凸显了对特定人群基因变异程度进行编目的必要性。更好地理解特定人群之间基因变异的差异有助于评估生活方式疾病的风险。

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