Minaguchi K
Department of Forensic Ondotology, Tokyo Dental College, Chiba City, Japan.
Electrophoresis. 1997 Oct;18(11):1923-7. doi: 10.1002/elps.1150181106.
The STR system D12S67 was amplified by polymerase chain reaction (PCR) and analyzed by denaturing gel electrophoresis followed by silver staining. Among 133 DNA samples from Japanese individuals, 11 alleles were observed and the heterozygosity was 80%. When sequences of the alleles were compared, each allelic segment contained 35-45 gata or gaca tetranucleotide repeats. Although a (gaca)n repeat block was concentrated in a defined region, nine different blocks of (gata)n repeats were observed separated by the (gaca)n repeat and single copy sequences. In addition, the allelic differences result from the total number of repeats of at least three (gata)n and the (gaca)n repeat regions. Novel primers overlapping part of the sequence with each other were constructed in the center of the D12S67 sequence, and the 5' and 3' segments were amplified by PCR. Both of these segments were highly polymorphic and showed heterozygosities of 77 and 78% with 7 and 10 alleles, respectively. The genotypes of the two polymorphisms were not concordant with the original polymorphism and the combination of the 5' and 3' side segment polymorphisms enabled further detailed classification of the D12S67 locus by simple comparison of the PCR product sizes. The number of the allele types increased up to 35 and the heterozygosity to 93%.
采用聚合酶链反应(PCR)扩增STR系统D12S67,并通过变性凝胶电泳及银染进行分析。在133份来自日本个体的DNA样本中,观察到11个等位基因,杂合度为80%。对等位基因序列进行比较时,每个等位基因片段包含35 - 45个gata或gaca四核苷酸重复序列。虽然一个(gaca)n重复序列块集中在一个特定区域,但观察到九个不同的(gata)n重复序列块被(gaca)n重复序列和单拷贝序列分隔开。此外,等位基因差异源于至少三个(gata)n重复序列和(gaca)n重复区域的重复序列总数。在D12S67序列中心构建了彼此部分重叠的新型引物,并通过PCR扩增5'和3'片段。这两个片段均具有高度多态性,分别显示出77%和78%的杂合度,等位基因数分别为7个和10个。这两种多态性的基因型与原始多态性不一致,5'和3'侧翼片段多态性的组合通过简单比较PCR产物大小实现了D12S67位点的进一步详细分类。等位基因类型数量增加到35个,杂合度增加到93%。