首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Genetic variation at the TNF-alpha promoter and malaria susceptibility in rhesus (Macaca mulatta) and long-tailed (Macaca fascicularis) macaques
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Genetic variation at the TNF-alpha promoter and malaria susceptibility in rhesus (Macaca mulatta) and long-tailed (Macaca fascicularis) macaques

机译:猕猴和长尾猕猴TNF-α启动子的遗传变异和疟疾易感性

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摘要

Polymorphisms within the promoter region of the TNF-alpha gene have been associated with altered expression of TNF-a and susceptibility to a variety of diseases in humans. Although macaques (Macaca spp.) are frequently used as models to study human diseases, little is known about the extent of genetic variation at the TNF-alpha locus and its consequences for disease susceptibility in these species. The TNF-alpha(x promoter region was sequenced in a sample of 40 macaques including five M. mulatta of Chinese and Indian ancestry and 35 M.fascicularis of Malaysian, Mauritian, Indonesian, and Philippine ancestry. These groups were chosen because they exhibit differences in their susceptibilities to severe malaria upon infection with Plasmodium parasites. Sequence analysis revealed a total of 14 single nucleotide polymorphisms (SNPs), five of which are newly described, and 20 unique haplotypes. In addition, the TFSEARCH program was used to investigate the potential of these polymorphisms to influence transcription factor binding. While both species exhibited a similarly high degree of genetic variability at the TNF-alpha promoter, AMOVA analysis and FST values indicated that most of the variation is shared between species and among populations. However, two of the most common haplotypes, describing 31.7% of the observed variation, and three potentially functional polymorphisms at positions -781, -535, and -10, were exclusive to M.fascicularis. Polymorphisms in the human ortholog of the TNF-alpha promoter which are known to be associated with malaria susceptibility in humans were not shared with macaques.
机译:TNF-α基因启动子区域内的多态性与TNF-α表达的改变和人类对多种疾病的易感性有关。尽管猕猴(Macaca spp。)经常用作研究人类疾病的模型,但对于TNF-α基因座的遗传变异程度及其对这些物种疾病易感性的影响知之甚少。在40只猕猴的样本中对TNF-α(x启动子区)进行了测序,包括中国和印度血统的5个鱼和马来西亚,毛里求斯,印度尼西亚和菲律宾血统的35个fa生的M. fascicularis。序列分析显示总共有14种单核苷酸多态性(SNP),其中有5种是新描述的,还有20种独特的单倍型,此外,还使用TFSEARCH程序研究了其潜在的易感性。这些多态性影响转录因子的结合,虽然两个物种在TNF-α启动子上都表现出相似的高度遗传变异性,但AMOVA分析和FST值表明,大多数变异在物种之间和种群之间共享。最常见的单倍型,描述了观察到的变异的31.7%,以及三个潜在的功能性多态性离子-781,-535和-10仅对fascicularis有用。猕猴并没有发现与人类疟疾易感性相关的TNF-α启动子在人类直系同源物中的多态性。

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