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首页> 外文期刊>Sociedade Brasileira de Medicina Tropical. Revista >Distribution of QPY and RAH haplotypes of granzyme B gene in distinct Brazilian populations
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Distribution of QPY and RAH haplotypes of granzyme B gene in distinct Brazilian populations

机译:不同巴西人群中颗粒酶B基因的QPY和RAH单倍型分布

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INTRODUCTION: The cytolysis mediated by granules is one of the most important effector functions of cytotoxic T lymphocytes and natural killer cells. Recently, three single nucleotide polymorphisms (SNPs) were identified at exons 2, 3, and 5 of the granzyme B gene, resulting in a haplotype in which three amino acids of mature protein Q48P88Y245 are changed to R48A88H245, which leads to loss of cytotoxic activity of the protein. In this study, we evaluated the frequency of these polymorphisms in Brazilian populations. METHODS: We evaluated the frequency of these polymorphisms in Brazilian ethnic groups (white, Afro-Brazilian, and Asian) by sequencing these regions. RESULTS: The allelic and genotypic frequencies of SNP 2364A/G at exon 2 in Afro-Brazilian individuals (42.3% and 17.3%) were significantly higher when compared with those in whites and Asians (p 0.0001 and p = 0.0007, respectively). The polymorphisms 2933C/G and 4243C/T also were more frequent in Afro-Brazilians but without any significant difference regarding the other groups. The Afro-Brazilian group presented greater diversity of haplotypes, and the RAH haplotype seemed to be more frequent in this group (25%), followed by the whites (20.7%) and by the Asians (11.9%), similar to the frequency presented in the literature. CONCLUSIONS: There is a higher frequency of polymorphisms in Afro-Brazilians, and the RAH haplotype was more frequent in these individuals. We believe that further studies should aim to investigate the correlation of this haplotype with diseases related to immunity mediated by cytotoxic lymphocytes, and if this correlation is confirmed, novel treatment strategies might be elaborated.
机译:简介:颗粒介导的细胞溶解是细胞毒性T淋巴细胞和自然杀伤细胞最重要的效应器功能之一。最近,在粒酶B基因的外显子2、3和5处鉴定出三个单核苷酸多态性(SNP),导致单倍型,其中成熟蛋白Q48P88Y245的三个氨基酸变为R48A88H245,这导致细胞毒活性丧失蛋白质。在这项研究中,我们评估了巴西人群中这些多态性的频率。方法:通过对这些区域进行测序,我们评估了巴西多族裔(白人,非裔巴西人和亚洲人)中这些多态性的频率。结果:与白人和亚洲人相比,非洲裔巴西人第2外显子的SNP 2364A / G等位基因和基因型频率(分别为42.3%和17.3%)显着更高(分别为p <0.0001和p = 0.0007)。在非洲裔巴西人中,多态性2933C / G和4243C / T也较常见,但在其他群体上没有任何显着差异。非洲裔巴西人组的单倍型多样性更高,该组中RAH单倍型似乎更为频繁(25%),其次是白人(20.7%)和亚洲人(11.9%),与所呈现的频率相似在文学中。结论:非洲裔巴西人中多态性的频率更高,而这些个体中RAH单倍型的频率更高。我们认为,进一步的研究应旨在研究这种单倍型与细胞毒性淋巴细胞介导的免疫相关疾病的相关性,如果这种相关性得到证实,可能会制定出新的治疗策略。

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