Kamiya H, Murata-Kamiya N, Koizume S, Inoue H, Nishimura S, Ohtsuka E
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Carcinogenesis. 1995 Apr;16(4):883-9. doi: 10.1093/carcin/16.4.883.
We previously reported that 8-hydroxyguanine (7,8-dihydro-8-oxoguanine) at the second position of codon 12 of the c-Ha-ras gene induces many types of mutations in NIH3T3 cells. In this study we incorporated the modified base into the first and second positions of codon 12 in the coding strand and into the first position of codon 61 in the non-coding strand of the gene using a new 8-hydroxyguanine phosphoramidite as a building block during oligonucleotide synthesis. The ras genes with 8-hydroxyguanine were transfected into NIH3T3 cells and the mutations induced were analyzed. 8-Hydroxyguanine residues at the first positions of codons 12 and 61 induced mutations to T at the modified sites almost exclusively. On the other hand, the DNA lesion at the second position of codon 12 induced a G-->A transition in addition to a G-->T transversion, confirming our previous results. Mutations in 5'-flanking sites were observed with 8-hydroxyguanine at the second position of codon 12 or the first position of codon 61. These results indicate that 8-hydroxyguanine in mammalian cells mainly induces a G-->T transversion at the modified site, but that other types of mutations are also elicited.
我们之前报道过,c-Ha-ras基因第12密码子第二位的8-羟基鸟嘌呤(7,8-二氢-8-氧代鸟嘌呤)在NIH3T3细胞中可诱导多种类型的突变。在本研究中,我们在寡核苷酸合成过程中,使用一种新的8-羟基鸟嘌呤亚磷酰胺作为构建模块,将修饰碱基掺入该基因编码链第12密码子的第一位和第二位以及非编码链第61密码子的第一位。将带有8-羟基鸟嘌呤的ras基因转染到NIH3T3细胞中,并对诱导产生的突变进行分析。第12和61密码子第一位的8-羟基鸟嘌呤残基几乎只在修饰位点诱导突变为T。另一方面,第12密码子第二位的DNA损伤除了诱导G→T颠换外,还诱导了G→A转换,证实了我们之前的结果。在第12密码子第二位或第61密码子第一位存在8-羟基鸟嘌呤时,在5'侧翼位点观察到了突变。这些结果表明,哺乳动物细胞中的8-羟基鸟嘌呤主要在修饰位点诱导G→T颠换,但也会引发其他类型的突变。