Sugano K, Kyogoku A, Fukayama N, Ohkura H, Shimosato Y, Sekiya T, Hayashi K
Division of Clinical Laboratory Oncology, National Cancer Center Hospital, Tokyo, Japan.
Lab Invest. 1993 Mar;68(3):361-6.
To achieve simple and rapid detection of codon 12 mutations of the c-Ki-ras2 gene, we developed a nonradioisotopic single-strand conformation polymorphism analysis using silver stain.
After a conventional polymerase chain reaction, amplified DNA fragments were mixed with formamide, heated and subjected to electrophoresis for 1.5 hours using minigels of polyacrylamide. The gels were then silver stained and single-strand DNA fragments were visualized directly.
Electrophoresis and subsequent silver staining were completed within 2.5 hours. Plasmids carrying various codon 12 mutations of the c-Ki-ras2 gene were used as controls of Nonradioisotopic single-strand confirmation polymorphism analysis, and all six mutations were successfully separated from the normal allele in a single electrophoretic run. In the analysis of tumor cell lines and tumor samples, the results were identical with those of conventional dot blot hybridization using 32P-labeled oligonucleotide probes. Of 10 colorectal carcinoma tissues examined, 4 tumors were shown to carry codon 12 mutations of the c-Ki-ras2 gene.
We conclude that this novel technique is a rapid, simple and useful method that may replace conventional methods.
为了实现对c-Ki-ras2基因第12密码子突变的简单快速检测,我们开发了一种使用银染的非放射性单链构象多态性分析方法。
经过常规聚合酶链反应后,将扩增的DNA片段与甲酰胺混合,加热,然后使用聚丙烯酰胺微型凝胶进行1.5小时的电泳。然后对凝胶进行银染,直接观察单链DNA片段。
电泳及随后的银染在2.5小时内完成。携带c-Ki-ras2基因各种第12密码子突变的质粒用作非放射性单链构象多态性分析的对照,在一次电泳中,所有六种突变均成功地与正常等位基因分离。在肿瘤细胞系和肿瘤样本的分析中,结果与使用32P标记的寡核苷酸探针进行的传统点杂交结果一致。在所检测的10例结肠直肠癌组织中,有4例肿瘤显示携带c-Ki-ras2基因第12密码子突变。
我们得出结论,这种新技术是一种快速、简单且有用的方法,可能会取代传统方法。