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不同人类单倍型中主要组织相容性复合体微卫星CL1的分析。

Analysis of the major histocompatibility complex microsatellite CL1 in different human haplotypes.

作者信息

Grimsley G, Ulgiati D, Abraham L J

机构信息

Department of Biochemistry, University of Western Australia, Nedlands, Australia.

出版信息

Eur J Immunogenet. 1996 Jun;23(3):205-9. doi: 10.1111/j.1744-313x.1996.tb00115.x.

Abstract

Characterization of the region between HLA-B and the TNF loci in the human MHC revealed the presence of duplicated loci, named CL1 and CL2, that included repeat sequences. Development and use of a PCR typing methodology that amplified both CL microsatellites simultaneously indicated that PCR product patterns analysed on native agarose gels were allelic (Abraham et al., 1992). The purpose of the current study was to determine the molecular explanation for the unique patterns achieved. Sequence analysis of the CL1 locus from 32 chromosomes representing 10 ancestral haplotypes indicated that six alleles were present. The CL microsatellites also provided an opportunity to study the evolutionary relationships between MHC haplotypes from different racial groups. Sequence comparison of closely related ancestral haplotypes from different racial groups suggested that the CL1 microsatellite has not changed in the period since divergence.

摘要

对人类主要组织相容性复合体(MHC)中HLA - B与肿瘤坏死因子(TNF)基因座之间区域的特征分析揭示了存在名为CL1和CL2的重复基因座,其中包含重复序列。一种能同时扩增两个CL微卫星的聚合酶链反应(PCR)分型方法的开发和应用表明,在天然琼脂糖凝胶上分析的PCR产物模式具有等位基因特征(亚伯拉罕等人,1992年)。本研究的目的是确定实现这些独特模式的分子解释。对代表10种祖先单倍型的32条染色体上的CL1基因座进行序列分析表明存在6个等位基因。CL微卫星还提供了一个研究不同种族群体MHC单倍型之间进化关系的机会。对不同种族群体密切相关的祖先单倍型进行序列比较表明,自分化以来,CL1微卫星没有发生变化。

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