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通过酶促扩增和寡核苷酸探针测定的不同人群中HLA-DQα等位基因和基因型频率。

HLA-DQ alpha allele and genotype frequencies in various human populations, determined by using enzymatic amplification and oligonucleotide probes.

作者信息

Helmuth R, Fildes N, Blake E, Luce M C, Chimera J, Madej R, Gorodezky C, Stoneking M, Schmill N, Klitz W

机构信息

Department of Human Genetics, Cetus Corporation, Emeryville, CA 94608.

出版信息

Am J Hum Genet. 1990 Sep;47(3):515-23.

Abstract

Allele and genotype frequencies at the HLA-DQ alpha locus have been determined by the use of polymerase chain reaction (PCR) amplification and nonradioactive oligonucleotide probes. The probes define six alleles and 21 genotypes in a dot-blot format. A total of over 1,400 individuals from 11 populations has been typed by two different laboratories using this method. In contrast to some variable-number-of-tandem-repeat markers that have been used for identity determination, DQ alpha genotype frequencies do not deviate significantly from Hardy-Weinberg equilibrium in all populations studied. The distribution of alleles varies significantly between most of these populations. In Caucasians, the allele frequencies range from 4.3% to 28.5%. In this population, the power of discrimination is .94, and, for paternity determination, the power of exclusion is .642. These population data will allow the use of the HLA-DQ alpha marker in paternity determination, the analysis of individual identity in forensic samples, and anthropological studies.

摘要

通过聚合酶链反应(PCR)扩增和非放射性寡核苷酸探针,已确定了HLA-DQα位点的等位基因和基因型频率。这些探针以斑点杂交形式定义了6个等位基因和21种基因型。两个不同实验室使用此方法对来自11个群体的总共1400多名个体进行了分型。与一些用于身份鉴定的可变串联重复标记不同,在所有研究的群体中,DQα基因型频率并未显著偏离哈迪-温伯格平衡。在大多数这些群体之间,等位基因的分布存在显著差异。在白种人中,等位基因频率范围为4.3%至28.5%。在该群体中,鉴别力为0.94,用于亲子鉴定时,排除力为0.642。这些群体数据将允许在亲子鉴定、法医样本个体身份分析和人类学研究中使用HLA-DQα标记。

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