Gao Q, Pang H M, Yeung E S
Ames Laboratory-USDOE and Department of Chemistry, Iowa State University, 50011, USA.
Electrophoresis. 1999 Jun;20(7):1518-26. doi: 10.1002/(SICI)1522-2683(19990601)20:7<1518::AID-ELPS1518>3.0.CO;2-5.
Short tandem repeat (STR) markers are highly polymorphic and widely used in human identification and genetic mapping. We demonstrate fast and reliable genotyping based on the four STR loci vWF, THO1, TPOX, CSF1PO by multiple-capillary array electrophoresis. Extracted human genomic DNA was amplified by polymerase chain reaction (PCR). The PCR products were mixed with pooled allelic ladder as an absolute standard and coinjected from a 96-vial tray. Separations were performed in polyvinylpyrrolidone (PVP) sieving matrix with a one-hour turnaround time, with no degradation over 27 runs. Simultaneous one-color laser-induced fluorescence detection was achieved by using a charge-coupled device (CCD) camera. The allele peaks for the unknown sample were identified by comparing the normalized peak intensities of the mixtures to those of the pooled ladder by using a straightforward algorithm. An extremely high level of confidence in matching the bands was indicated with negligible crosstalk (< 0.89%) between adjacent capillaries. This scheme is applicable for STR genotyping with high resolution, high speed and high throughput.
短串联重复序列(STR)标记具有高度多态性,广泛应用于人类身份识别和基因图谱绘制。我们通过多毛细管阵列电泳展示了基于四个STR基因座vWF、THO1、TPOX、CSF1PO的快速可靠基因分型。提取的人类基因组DNA通过聚合酶链反应(PCR)进行扩增。PCR产物与混合等位基因阶梯作为绝对标准混合,并从96孔板中同时进样。在聚乙烯吡咯烷酮(PVP)筛分基质中进行分离,周转时间为一小时,在27次运行中无降解。使用电荷耦合器件(CCD)相机实现了同步单色激光诱导荧光检测。通过使用一种简单的算法,将混合物的归一化峰强度与混合阶梯的峰强度进行比较,从而识别未知样品的等位基因峰。相邻毛细管之间的串扰可忽略不计(<0.89%),这表明在匹配条带方面具有极高的置信度。该方案适用于高分辨率、高速和高通量的STR基因分型。