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厄瓜多尔卡亚帕印第安人的HLA II类单倍型分析:一个新的DRB1等位基因揭示了86位存在趋同进化和平衡选择的证据。

Analysis of HLA class II haplotypes in the Cayapa Indians of Ecuador: a novel DRB1 allele reveals evidence for convergent evolution and balancing selection at position 86.

作者信息

Titus-Trachtenberg E A, Rickards O, De Stefano G F, Erlich H A

机构信息

Department of Human Genetics, Roche Molecular Systems, Alameda, CA 94618.

出版信息

Am J Hum Genet. 1994 Jul;55(1):160-7.

Abstract

PCR amplification, oligonucleotide probe typing, and sequencing were used to analyze the HLA class II loci (DRB1, DQA1, DQB1, and DPB1) of an isolated South Amerindian tribe. Here we report HLA class II variation, including the identification of a new DRB1 allele, several novel DR/DQ haplotypes, and an unusual distribution of DPB1 alleles, among the Cayapa Indians (N = 100) of Ecuador. A general reduction of HLA class II allelic variation in the Cayapa is consistent with a population bottle-neck during the colonization of the Americas. The new Cayapa DRB1 allele, DRB108042, which arose by a G-->T point mutation in the parental DRB10802, contains a novel Val codon (GTT) at position 86. The generation of DRB108042 (Val-86) from DRB10802 (Gly-86) in the Cayapa, by a different mechanism than the (GT-->TG) change in the creation of DRB108041 (Val-86) from DRB10802 in Africa, implicates selection in the convergent evolution of position 86 DR beta variants. The DRB108042 allele has not been found in > 1,800 Amerindian haplotypes and thus presumably arose after the Cayapa separated from other South American Amerindians. Selection pressure for increased haplotype diversity can be inferred in the generation and maintenance of three new DRB108042 haplotypes and several novel DR/DQ haplotypes in this population. The DPB1 allelic distribution in the Cayapa is also extraordinary, with two alleles, DPB11401, a very rare allele in North American Amerindian populations, and DPB10402, the most common Amerindian DPB1 allele, constituting 89% of the Cayapa DPB1.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用聚合酶链反应(PCR)扩增、寡核苷酸探针分型和测序技术,对一个与世隔绝的南美印第安部落的人类白细胞抗原(HLA)Ⅱ类基因座(DRB1、DQA1、DQB1和DPB1)进行分析。在此,我们报告了厄瓜多尔卡亚帕印第安人(N = 100)中HLAⅡ类基因的变异情况,包括一个新的DRB1等位基因的鉴定、几种新的DR/DQ单倍型以及DPB1等位基因的异常分布。卡亚帕人群中HLAⅡ类等位基因变异的普遍减少与美洲殖民时期的种群瓶颈一致。新的卡亚帕DRB1等位基因DRB108042由亲本DRB10802发生G→T点突变产生,在第86位含有一个新的缬氨酸密码子(GTT)。卡亚帕人群中由DRB10802(甘氨酸-86)产生DRB108042(缬氨酸-86)的机制,与非洲人群中由DRB10802产生DRB108041(缬氨酸-86)时发生的(GT→TG)变化不同,这暗示了第86位DRβ变体趋同进化过程中的选择作用。在超过1800个美洲印第安单倍型中未发现DRB108042等位基因,因此推测它是在卡亚帕人与其他南美印第安人分离后出现的。在该人群中三种新的DRB108042单倍型和几种新的DR/DQ单倍型的产生及维持过程中,可以推断存在增加单倍型多样性的选择压力。卡亚帕人群中DPB1等位基因的分布也很特别,两个等位基因,北美印第安人群中非常罕见的DPB11401和美洲印第安人群中最常见的DPB1等位基因DPB10402,占卡亚帕DPB1的89%。(摘要截短于250字)

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本文引用的文献

1
HLA-DR beta chain residue 86 controls DR alpha beta dimer stability.
Eur J Immunol. 1993 Jun;23(6):1346-50. doi: 10.1002/eji.1830230624.

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