Schneider P M, Meuser S, Waiyawuth W, Seo Y, Rittner C
Institute of Legal Medicine, Johannes Gutenberg University, Mainz, Germany.
Forensic Sci Int. 1998 Oct 12;97(1):61-70. doi: 10.1016/s0379-0738(98)00146-7.
The Y-chromosomal short tandem repeat (STR) locus DYS385 can be typed using PCR amplification and separation of the resulting polymorphic fragments by non-denaturing high resolution polyacrylamide gel electrophoresis followed by silver staining. The PCR primers amplify a duplicated repeat sequence on the Y chromosome revealing a two-band pattern in male individuals. To determine the internal repeat structure as a basis for a consensus nomenclature, DNA sequence analysis was carried out after subcloning of PCR-amplified fragments revealing the uniform 4-bp repeat structure 'GAAA'. The shortest allele observed consisted of 10 repeat units thus providing the basis for the designation 'allele 10'. Except for isolated point mutations, no systematic differences could be observed either in the repeat sequence or in the flanking regions between the two fragments of a given individual. Thus it was not possible to discriminate between the two loci of the DYS385 system. Four population samples of German (n = 146), Chinese (n = 100), Japanese (n = 100), and Thai (n = 95) origin were studied. In the four groups, alleles 10 to 24 could be observed and genotype frequencies differed significantly. In Germans only one common genotype was present (11-14; 33.8% frequency). In the Asian populations, the frequencies were more evenly distributed with the 13-13 genotype (9%) in Chinese, the 13-17 genotype (14%) in Japanese and the 14-18 genotype (7%) in Thai being the most common. Overall, 69 different genotypes were found, of these 36 were observed in Germans, 36 in Chinese, 33 in Japanese and 44 in Thai. No mutations were detected in 62 father-son pairs. Thus DYS385 is a highly polymorphic STR system with population-specific genotype distributions.
Y染色体短串联重复序列(STR)位点DYS385可通过聚合酶链反应(PCR)扩增,并采用非变性高分辨率聚丙烯酰胺凝胶电泳分离所得多态性片段,随后进行银染来分型。PCR引物扩增Y染色体上的重复序列,在男性个体中呈现出两条带的模式。为确定内部重复结构以作为统一命名法的基础,在对PCR扩增片段进行亚克隆后进行DNA序列分析,结果显示其具有统一的4碱基重复结构“GAAA”。观察到的最短等位基因由10个重复单元组成,因此为命名“等位基因10”提供了依据。除了个别点突变外,在给定个体的两个片段之间,重复序列或侧翼区域均未观察到系统差异。因此,无法区分DYS385系统的两个位点。研究了来自德国(n = 146)、中国(n = 100)、日本(n = 100)和泰国(n = 95)的四个人群样本。在这四组人群中,可观察到等位基因10至24,且基因型频率存在显著差异。在德国人中,仅存在一种常见基因型(11 - 14;频率为33.8%)。在亚洲人群中,频率分布更为均匀,中国人中最常见的基因型是13 - 13(频率为9%),日本人中是13 - 17(频率为14%),泰国人中是14 - 18(频率为7%)。总体而言,共发现69种不同基因型,其中德国人中有36种,中国人中有36种,日本人中有33种,泰国人中有44种。在62对父子对中未检测到突变。因此,DYS385是一个具有人群特异性基因型分布的高度多态性STR系统。