Pablo V Gejman , Qiuhe Cao , Françoise Guedj , Steve Sommer
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引用次数: 32
Abstract
Denaturing gradient gel electrophoresis (DGGE) is considered one of the most sensitive and specific of the mutational scanning techniques, yet blinded analyses have not been reported. We report the results of a blinded study of the efficiency of DGGE to detect mutations in the Human Coagulation Factor IX. Two overlapping genomic DNA sequences from exon 8 of Factor IX (290 bp and 539 bp length) with an unknown number of mutations were amplified with a 40 bp GC-clamp and tested blindly by DGGE. DGGE detected all mutations in the 290 bp genomic DNA segment. DGGE detected all but one mutation in the 539 bp genomic segment after experimental conditions were fully optimized but missed multiple mutations in an initial blinded experiment. These results demonstrate the utility of blinded analyses and confirm the exquisite power of DGGE for detecting mutations.
变性梯度凝胶电泳(DGGE)被认为是最敏感和特异的突变扫描技术之一,但盲法分析尚未报道。我们报告了DGGE检测人凝血因子IX突变效率的盲法研究结果。用40 bp GC-clamp扩增因子IX外显子8的两个重叠的基因组DNA序列(290 bp和539 bp长度),突变数未知,并进行DGGE盲测。DGGE检测到290bp基因组DNA片段的所有突变。在实验条件完全优化后,DGGE检测到了539bp基因组片段中除1个突变外的所有突变,但在最初的盲法实验中遗漏了多个突变。这些结果证明了盲法分析的实用性,并证实了DGGE在检测突变方面的卓越能力。