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D17S5基因座等位基因的PCR扩增:在澳大利亚人群调查中通过寡核苷酸探针检测新的和罕见的长片段等位基因。

PCR amplification of alleles at locus D17S5: detection of new and rare long-length alleles by oligoprobing in a survey of Australian populations.

作者信息

Kijas J M, Fowler J C, Van Daal A

机构信息

School of Biological Sciences, Flinders University of South Australia, Adelaide.

出版信息

Hum Biol. 1994 Apr;66(2):329-37.

PMID:8194850
Abstract

Alleles of the hypervariable human locus D17S5 were amplified by polymerase chain reaction (PCR) and categorized by length. Unlike other surveys of this locus, the products of amplification were authenticated by Southern analysis using an oligomeric probe directed to part of the 70-base-pair (bp) variable number of tandem repeat (VNTR) region. A small number of unusually long alleles were located. In a survey of 201 unrelated Caucasian individuals, 16 alleles (size range, 170-1430 bp) and 59 genotypes were observed (heterozygosity, 86.4%; discriminating power, 0.963). In a similar survey of 166 traditional Australian aboriginals, 18 alleles (size range, 170-1430 bp) and 46 genotypes were found (heterozygosity, 80.8%; discriminating power, 0.942). The allele frequencies differed significantly between these two ethnically distinct populations. Comparisons are made with other anthropologically diverse populations.

摘要

通过聚合酶链反应(PCR)扩增人高变基因座D17S5的等位基因,并按长度进行分类。与该基因座的其他研究不同,扩增产物通过Southern分析进行验证,使用的寡聚探针针对70个碱基对(bp)可变串联重复序列(VNTR)区域的一部分。发现了少数异常长的等位基因。在对201名无亲缘关系的高加索个体的研究中,观察到16个等位基因(大小范围为170 - 1430 bp)和59种基因型(杂合度为86.4%;鉴别力为0.963)。在对166名传统澳大利亚原住民的类似研究中,发现了18个等位基因(大小范围为170 - 1430 bp)和46种基因型(杂合度为80.8%;鉴别力为0.942)。这两个人口在种族上明显不同的群体之间的等位基因频率存在显著差异。还与其他人类学上不同的群体进行了比较。

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