Lorente J A, Lorente M, Budowle B, Wilson M R, Villanueva E
Department of Legal Medicine, University of Granada, Spain.
Forensic Sci Int. 1994 May 13;65(3):169-75. doi: 10.1016/0379-0738(94)90272-0.
Amplification by polymerase chain reaction (PCR) of variable number of tandem repeat (VNTR) loci and subsequent typing by electrophoresis and silver staining has become a useful tool for identity testing. One viable group of genetic markers amenable to amplification by PCR is the short tandem repeat (STR) loci. A horizontal discontinuous polyacrylamide gel electrophoresis (PAGE) method was used to type the amplified products of the STR HUMVWA. Typing for VWA of 120 unrelated Spanish Caucasians was done. Six alleles were observed with frequencies in the range 0.096-0.242. The genotype distribution meets Hardy-Weinberg expectations (0.25 < P < 0.50). The heterozygosity was 73.3% and the discrimination power (DP) 0.94. Simultaneously, in a small sample of families (n = 24) no new mutations could be found.
通过聚合酶链反应(PCR)扩增可变数目串联重复序列(VNTR)位点,随后进行电泳和银染分型,已成为个体识别检测的一种有用工具。一类适合通过PCR扩增的可行基因标记是短串联重复序列(STR)位点。采用水平不连续聚丙烯酰胺凝胶电泳(PAGE)方法对STR HUMVWA的扩增产物进行分型。对120名无关的西班牙白种人进行了VWA分型。观察到6个等位基因,频率范围为0.096 - 0.242。基因型分布符合哈迪-温伯格预期(0.25 < P < 0.50)。杂合度为73.3%,鉴别力(DP)为0.94。同时,在一小部分家庭样本(n = 24)中未发现新的突变。