Kaufman E R, Davidson R L
Somatic Cell Genet. 1979 Sep;5(5):653-63. doi: 10.1007/BF01542701.
The effects of purine deoxyribonucleosides on bromodeoxyurdine (BrdU) mutagenesis in Syrian hamster melanoma cells were determined. Both deoxyguanosine (dG) and deoxyadenosine (dA) were found to stimulate mutagenesis without changing the amount of BrdU in DNA. In addition, the stimulation of mutagenesis by dG and dA was suppressed by the addition of deoxycytidine (dC). These results suggest that BrdU mutagenesis involves the perturbation of dC metabolism, which perturbation is enhanced by dGTP and dATP. The mutagenic activity of dG in the absence of BrdU was tested, as was that of thymidine (dT), which we had shown previously to stimulate BrdU mutageneis. With dG alone, no increase above the spontaneous mutation frequency was detected. However, at extremely high concentration, dT in the absence of BrdU was slightly mutagenic, and the mutagenesis by dT was enhanced by dG and suppressed by dC.
测定了嘌呤脱氧核糖核苷对叙利亚仓鼠黑色素瘤细胞中溴脱氧尿苷(BrdU)诱变作用的影响。发现脱氧鸟苷(dG)和脱氧腺苷(dA)均能刺激诱变作用,而不改变DNA中BrdU的含量。此外,添加脱氧胞苷(dC)可抑制dG和dA对诱变作用的刺激。这些结果表明,BrdU诱变涉及dC代谢的扰动,而dGTP和dATP可增强这种扰动。测试了在不存在BrdU的情况下dG的诱变活性,以及胸腺嘧啶核苷(dT)的诱变活性,我们之前已证明dT可刺激BrdU诱变。单独使用dG时,未检测到高于自发突变频率的增加。然而,在极高浓度下,不存在BrdU时dT具有轻微的诱变作用,dG可增强dT的诱变作用,而dC可抑制其诱变作用。