Oldroyd N J, Urquhart A J, Kimpton C P, Millican E S, Watson S K, Downes T, Gill P D
Forensic Science Service, North, Birmingham, UK.
Electrophoresis. 1995 Mar;16(3):334-7. doi: 10.1002/elps.1150160155.
Through the use of fluorescence-based polymerase chain reaction systems, a highly discriminating multiplex with the potential for individual identification has been developed. The use of multiple dye technology enabling loci with overlapping size ranges to be co-amplified has enabled us to successfully amplify seven tetranucleotide short tandem repeat loci within a single reaction resulting in a discriminating power in the region of 1 x 10(9). Three out of the seven loci employed exhibit alleles differing in size by only 2 bp as opposed to the conventional 4 bp, which results in such loci being more powerful in terms of distinguishing between samples, particularly when co-amplified in this manner. The size ranges of the loci contained within the system are such that windows still exist for the inclusion of additional loci at a later stage, which could increase the discriminating power of the system still further. In addition, further weight and utility is lent to the system through the incorporation of a simple and reliable sex test involving the amplification of a segment of the X-Y homologous gene Amelogenin.
通过使用基于荧光的聚合酶链反应系统,已开发出一种具有高度鉴别力且有个体识别潜力的多重检测方法。采用多染料技术能够对大小范围重叠的基因座进行共扩增,这使我们能够在单个反应中成功扩增七个四核苷酸短串联重复基因座,鉴别力达到1×10⁹左右。所采用的七个基因座中有三个的等位基因大小仅相差2 bp,而非传统的4 bp,这使得这些基因座在区分样本方面更具效力,尤其是以这种方式进行共扩增时。该系统内基因座的大小范围使得后续仍有空间纳入更多基因座,这可能会进一步提高系统的鉴别力。此外,通过纳入一个简单可靠的性别检测(涉及对X - Y同源基因牙釉蛋白一段序列的扩增),该系统的重要性和实用性得到了进一步提升。