Klintschar M, Ebner A, Reichenpfader B
Department of Legal Medicine, University of Graz, Austria.
Electrophoresis. 1999 Jun;20(8):1740-2. doi: 10.1002/(SICI)1522-2683(19990101)20:8<1740::AID-ELPS1740>3.0.CO;2-C.
The short tandem repeats (STR) D3S1358, VWA, FGA, D8S1179, D21S11, D18S51, D5S818, D13S317, D7S820 and a locus allowing sex discrimination (amelogenin) can be coamplified by the polymerase chain reaction using a commercially available kit, and subsequently typed using capillary electrophoresis. To establish databases for these loci for Austrian Caucasians, 115 unrelated persons were typed. All loci were in Hardy-Weinberg equilibrium. The combined mean paternity exclusion chance (MEC) was 0.999891 and the combined discriminating power (DP) was 3.08 x 10(-11). The allelic distributions showed no differences to those found for other Caucasian populations. Our data differed significantly from an Afro-American population at 5 loci and from a Chinese population at 4 loci. Linkage disequilibrium between any of the coamplified loci was not evident. Thus the combination of multiplex PCR and capillary electrophoresis can save time and yield excellent results for paternity testing and stain analysis.
短串联重复序列(STR)D3S1358、VWA、FGA、D8S1179、D21S11、D18S51、D5S818、D13S317、D7S820以及一个用于性别鉴定的位点(牙釉蛋白),可使用市售试剂盒通过聚合酶链反应进行共扩增,随后采用毛细管电泳进行分型。为建立奥地利高加索人的这些位点数据库,对115名无关个体进行了分型。所有位点均处于哈迪-温伯格平衡。联合平均父权排除率(MEC)为0.999891,联合鉴别力(DP)为3.08×10⁻¹¹。等位基因分布与其他高加索人群的分布无差异。我们的数据在5个位点上与非裔美国人种群显著不同,在4个位点上与中国人群显著不同。共扩增位点之间未发现连锁不平衡。因此,多重聚合酶链反应和毛细管电泳相结合可为亲子鉴定和污渍分析节省时间并产生优异结果。