Krausa P, Carcassi C, Orrù S, Bodmer J G, Browning M J, Contu L
ICRF, Institute of Molecular Medicine, Oxford, UK.
Hum Immunol. 1995 Sep;44(1):35-42. doi: 10.1016/0198-8859(95)00046-7.
HLA-A30 is present in the Sardinian population at a frequency of 23%. We have designed a system using nested ARMS-PCR to determine the relative frequencies of the HLA-A30 allelic variants (A3001, A3002, and A3003) within this population. The use of a nested PCR approach, in which the first-round reaction provides HLA-A30 specificity and template DNA for the subsequent nested reactions, is a powerful means of discriminating between alleles of very similar sequence. Using this method, we performed subtyping of 35 serologically defined HLA-A30 Sardinian individuals, and taking into account homozygotes, identified 38 A30 alleles. Of these, 33 typed as A3002, four typed as A3001, and one sample did not conform to the patterns of reactivity of any of the published A30 alleles. Haplotype information showed strong linkage disequilibrium between A3002 and B18. This study underlines the potential of DNA-based methods for typing HLA class I in terms of adding further levels of definition to studies of population structure and also as a means of identifying new alleles.
HLA - A30在撒丁岛人群中的出现频率为23%。我们设计了一种使用巢式ARMS - PCR的系统,以确定该人群中HLA - A30等位基因变体(A3001、A3002和A3003)的相对频率。使用巢式PCR方法,其中第一轮反应为后续巢式反应提供HLA - A30特异性和模板DNA,是区分序列非常相似的等位基因的有力手段。使用这种方法,我们对35名血清学定义的HLA - A30撒丁岛个体进行了亚型分析,并考虑到纯合子,鉴定出38个A30等位基因。其中,33个分型为A3002,4个分型为A3001,1个样本不符合任何已发表的A30等位基因的反应模式。单倍型信息显示A3002和B18之间存在强连锁不平衡。这项研究强调了基于DNA的方法在HLA I类分型方面的潜力,即在为群体结构研究增加进一步的定义水平以及作为识别新等位基因的手段方面。