Casadei S, Cortesi L, Pensotti V, Radice P, Pierotti M, Amadori D, Calistri D
Istituto Oncologico Romagnolo, 47100 Forlì, Italy.
Br J Cancer. 2001 Sep 14;85(6):845-9. doi: 10.1054/bjoc.2001.1988.
We describe the Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method set up for a sensitive and preliminary rapid screening of BRCA1 mutations. We analysed exons 11 and 16, which are known to cover slightly more than 70% of the whole coding region of the gene, subdivided into 4 amplicons and labelled with different fluorescent dUTPs. MD-CFLP was first utilised on a panel of 30 DNA samples in which the presence of single-base substitutions or small deletions/insertions had been previously identified by direct sequencing as gold standard, in order to define the optimal conditions in terms of PCR amplification and temperature of digestion. In a second step, we blindly analysed 21 DNA samples by MD-CFLP to verify its reliability. The sensitivity and specificity of MD-CFLP were both 100% in the first study, and 80% and 94%, respectively, in the blind sample assay. Our results demonstrate the capability of the MD-CFLP method to detect DNA sequence alterations in fragments of more than 1 kb. We conclude that CFLP is a powerful tool in mutational analysis, offering reliable results in a shorter time and at a lower cost than conventional methods, and its potential can be enhanced when internal fluorescent labelling and laser detection are used.
我们描述了用于敏感且初步快速筛查BRCA1突变的多染料裂解酶片段长度多态性(MD-CFLP)方法。我们分析了第11和16外显子,已知这两个外显子覆盖该基因整个编码区的70%多一点,将其细分为4个扩增子并用不同的荧光dUTP进行标记。MD-CFLP首先应用于一组30个DNA样本,其中单碱基取代或小的缺失/插入的存在先前已通过直接测序作为金标准确定,以便确定PCR扩增和消化温度方面的最佳条件。第二步,我们通过MD-CFLP盲目分析了21个DNA样本以验证其可靠性。在第一项研究中MD-CFLP的敏感性和特异性均为100%,在盲样检测中分别为80%和94%。我们的结果证明了MD-CFLP方法检测超过1kb片段中DNA序列改变的能力。我们得出结论,CFLP是突变分析中的一种强大工具,与传统方法相比能在更短时间内以更低成本提供可靠结果,并且当使用内部荧光标记和激光检测时其潜力可以增强。