Zeillinger R, Schneeberger C, Speiser P, Kury F
First Department of Obstetrics & Gynecology, University of Vienna Medical School, Austria.
Biotechniques. 1993 Jul;15(1):89-95.
We describe the use of high-performance liquid chromatography (HPLC) for the rapid quantitative analysis of short DNA fragments generated in differential PCR, where a target gene and a control gene are in vitro coamplified in one single reaction. Using an anion-exchange nonporous column, both separation and quantitation of the differential PCR products are achieved in about 5 min per sample. The performance of this technique proved to be superior to that of conventional gel electrophoresis and subsequent analysis by a laser densitometer, a solid-state scanner and a charge coupled device video camera imaging system. The usefulness for clinical testing is described in the example of the quantitative analysis of the c-erbB-2 oncogene copy number of human breast carcinomas by differential PCR. The combined use of differential PCR and automated HPLC analysis of the PCR products may well substitute for classical Southern blot hybridization in routine clinical analysis of oncogene amplification.
我们描述了使用高效液相色谱法(HPLC)对差异PCR中产生的短DNA片段进行快速定量分析的方法,其中靶基因和对照基因在一个单一反应中进行体外共扩增。使用阴离子交换无孔柱,每个样品的差异PCR产物的分离和定量大约在5分钟内即可完成。事实证明,该技术的性能优于传统的凝胶电泳以及随后使用激光密度计、固态扫描仪和电荷耦合器件摄像机成像系统进行的分析。通过对人乳腺癌c-erbB-2癌基因拷贝数进行差异PCR定量分析的实例,阐述了该技术在临床检测中的实用性。差异PCR与PCR产物的自动HPLC分析相结合,很可能在癌基因扩增的常规临床分析中替代经典的Southern印迹杂交。