Makino R, Yazyu H, Kishimoto Y, Sekiya T, Hayashi K
Oncogene Division, National Cancer Center Research Institute, Tokyo, Japan.
PCR Methods Appl. 1992 Aug;2(1):10-3. doi: 10.1101/gr.2.1.10.
A fluorescence-based method for polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) analysis, F-SSCP, was developed in which the target sequence is amplified by the PCR using fluorescent primers. The amplified products are then heat-denatured and applied to a water-jacket controlled gel in an automated DNA sequencer. The separated strands are detected as laser-excited fluorescence at the bottom of the gel, and mutations are detected as shifts in the position of the peaks in the fluorogram. The system does not involve radioactivity, and the conditions of electrophoresis are more strictly controlled than in the previous system, which relied on ambient air-cooling to maintain the gel at a constant temperature. The nature of the output data allows direct quantitative interpretation, and so the relative abundance of each allele in a mixture of two or more alleles can easily be estimated. The application of F-SSCP for detection of mutations and loss of heterozygosities of p53 in tumor tissues is reported.
开发了一种基于荧光的聚合酶链反应-单链构象多态性(PCR-SSCP)分析方法,即F-SSCP,其中使用荧光引物通过PCR扩增靶序列。然后将扩增产物进行热变性,并应用于自动DNA测序仪中的水套控制凝胶。分离的链在凝胶底部作为激光激发荧光进行检测,突变则作为荧光图谱中峰位置的偏移进行检测。该系统不涉及放射性,并且与之前依赖环境空气冷却来维持凝胶恒温的系统相比,电泳条件得到了更严格的控制。输出数据的性质允许直接进行定量解释,因此可以轻松估计两个或多个等位基因混合物中每个等位基因的相对丰度。报道了F-SSCP在肿瘤组织中检测p53突变和杂合性缺失的应用。