因子V Leiden突变的快速DNA筛选程序的发展。

G A Scobie, S T Ho, G Dolan, N A Kalsheker
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引用次数: 10

摘要

目的:建立一种基于扩增难解突变系统(ARMS)的快速、简便、高特异性的DNA筛查方法,检测全血中Leiden突变。方法:构建-2或-3附加错配的arms PCR扩增引物,检测凝血结果异常患者全血中正常因子V基因和Leiden突变,大大提高特异性。结果构建的ARMS引物在引物3'端添加-2或-3错配,可在3小时内检测0.5 μ l全血中的Leiden突变。在-3位置失稳的引物可以在较低的退火温度下使用,这提供了更高的灵敏度,现在通常使用。在同一反应中加入一组对照引物作为阳性对照。结论:这种快速、特异的因子V Leiden突变检测方法是对血栓性血管疾病患者或有血栓性血管疾病风险患者进行调查的有用补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a rapid DNA screening procedure for the Factor V Leiden mutation.

Aim-To develop a rapid, simple and highly specific DNA screening procedure based on the amplification refractory mutation system (ARMS) to detect the Leiden mutation in whole blood.Methods-ARMS PCR amplification primers with additional mismatches at either -2 or -3, which greatly improves specificity, were constructed to detect the normal Factor V gene and the Leiden mutation in whole blood samples from patients with abnormal clotting results.Results-Construction of ARMS primers with either an additional mismatch at -2 or -3 at the 3' end of the primer could be used to detect the Leiden mutation in 0.5 mu1 whole blood in under three hours. Primers destabilised at position -3 could be used at a lower annealing temperature, which gave greater sensitivity and are now routinely used. A control set of primers was included in the same reaction to act as a positive control.Conclusions-This rapid and specific assay for the factor V Leiden mutation is a useful addition to the investigation of patients with or at risk from thrombovascular disease.

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