Kamiya H, Miura H, Murata-Kamiya N, Ishikawa H, Sakaguchi T, Inoue H, Sasaki T, Masutani C, Hanaoka F, Nishimura S
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Nucleic Acids Res. 1995 Aug 11;23(15):2893-9. doi: 10.1093/nar/23.15.2893.
An oligodeoxyribonucleotide containing 8-hydroxyadenine (OH8Ade) was chemically synthesized and single- and double-stranded c-Ha-ras gene fragments with OH8Ade at the second position of codon 61 were prepared. The single-stranded ras gene fragment was used as a template for in vitro DNA synthesis with the Klenow fragment of Escherichia coli DNA polymerase I, Taq DNA polymerase, rat DNA polymerase beta and mouse DNA polymerase alpha. The former two enzymes exclusively incorporated dTMP opposite OH8Ade. The DNA polymerases alpha and beta misinserted dGMP, and dAMP and dGMP, respectively. The c-Ha-ras gene was constructed using the double-stranded ras gene fragment containing OH8Ade and was transfected into NIH 3T3 cells. The gene with OH8Ade induced focus formation, indicating that OH8Ade elicited point mutations in cells. When c-Ha-ras genes present in transformed cells were analyzed, an A-->G transition and an A-->C transversion were detected. These results indicate that OH8Ade induced misincorporation in in vitro DNA synthesis and mutations in mammalian cells.
化学合成了一种含有8-羟基腺嘌呤(OH8Ade)的寡脱氧核糖核苷酸,并制备了密码子61第二位带有OH8Ade的单链和双链c-Ha-ras基因片段。单链ras基因片段用作模板,用大肠杆菌DNA聚合酶I的Klenow片段、Taq DNA聚合酶、大鼠DNA聚合酶β和小鼠DNA聚合酶α进行体外DNA合成。前两种酶在OH8Ade相对位置专一性地掺入dTMP。DNA聚合酶α和β分别错误插入dGMP以及dAMP和dGMP。使用含有OH8Ade的双链ras基因片段构建c-Ha-ras基因,并将其转染到NIH 3T3细胞中。含有OH8Ade的基因诱导了集落形成,表明OH8Ade在细胞中引发了点突变。当分析转化细胞中存在的c-Ha-ras基因时,检测到A→G转换和A→C颠换。这些结果表明,OH8Ade在体外DNA合成中诱导错误掺入,并在哺乳动物细胞中诱导突变。