Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan.
Mutat Res. 2010 Apr 1;686(1-2):90-5. doi: 10.1016/j.mrfmmm.2010.02.001. Epub 2010 Feb 12.
The formation of 8-hydroxyguanine (8-OH-Gua, 7,8-dihydro-8-oxoguanine) in DNA and in the nucleotide pool results in G:C-->T:A and A:T-->C:G substitution mutations, respectively, due to the ability of 8-OH-Gua to pair with both C and A. In this study, shuttle plasmid DNAs containing 8-OH-Gua paired with C and A in the supF gene were transfected into human 293T cells, in which specialized DNA polymerases were knocked-down. The DNAs replicated in the cells were recovered and then introduced into an indicator strain of Escherichia coli. Mutation analysis indicated that the knock-downs of DNA polymerases eta and zeta by siRNAs enhanced the G:C-->T:A mutations caused by 8-OH-Gua:C. The 8-OH-Gua:C-induced mutation frequency was not further increased by double knock-downs of DNA polymerases eta and zeta, suggesting that the two DNA polymerases work in the same pathway. In addition, the reduction of DNA polymerase eta slightly decreased the A:T-->C:G substitutions caused by 8-OH-Gua:A. These results suggest that DNA polymerases eta and zeta are involved in the bypass of 8-OH-Gua in human cells.
8-羟基鸟嘌呤(8-OH-Gua,7,8-二氢-8-氧鸟嘌呤)在 DNA 中和核苷酸池中形成,分别导致 G:C-->T:A 和 A:T-->C:G 取代突变,这是由于 8-OH-Gua 能够与 C 和 A 配对。在这项研究中,将含有 8-OH-Gua 与 C 和 A 配对的穿梭质粒 DNA 转染到人类 293T 细胞中,其中专门的 DNA 聚合酶被敲低。在细胞中复制的 DNA 被回收,然后引入大肠杆菌的指示菌株。突变分析表明,siRNA 对 DNA 聚合酶 eta 和 zeta 的敲低增强了 8-OH-Gua:C 引起的 G:C-->T:A 突变。8-OH-Gua:C 诱导的突变频率不会因 DNA 聚合酶 eta 和 zeta 的双重敲低而进一步增加,这表明这两种 DNA 聚合酶在相同的途径中工作。此外,DNA 聚合酶 eta 的减少略微降低了 8-OH-Gua:A 引起的 A:T-->C:G 取代。这些结果表明,DNA 聚合酶 eta 和 zeta 参与了人类细胞中 8-OH-Gua 的旁路。