Ong T, Converse J O
Mutat Res. 1983 Oct;124(1):61-7. doi: 10.1016/0165-1218(83)90185-4.
The excision repair-deficient genetic marker uvs-2 was crossed into the tester strains N23 and N24 of Neurospora crassa. Comparison was made among the effects of selected mutagens on a repair-sufficient strain (N23 or N24) and a repair-deficient strain (N23 uvs-2 or N24 uvs-2) with regard to cell killing and induction of reverse mutation from adenine dependence to adenine independence. Methyl methanesulfonate (MMS), ethyl methanesulfonate (EMS), 1,2,7,8-diepoxyoctane (DEO), N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), 2,3,5,6-tetraethyleneimino-1,4-benzoquinone (TEB) and ICR-170 were found to be more toxic to the repair-deficient strains than to the repair-sufficient strains. For the induction of reverse mutations N23 uvs-2 appeared to be more sensitive than N23 to MNNG and TEB and to the high concentrations of MMS and DEO while N24 was 20 times more sensitive than N24 uvs-2 to ICR-170.
将切除修复缺陷型遗传标记uvs - 2导入粗糙脉孢菌的测试菌株N23和N24中。就细胞杀伤以及腺嘌呤依赖性向腺嘌呤非依赖性的回复突变诱导情况而言,对选定诱变剂在修复充足菌株(N23或N24)和修复缺陷菌株(N23 uvs - 2或N24 uvs - 2)中的作用进行了比较。发现甲磺酸甲酯(MMS)、乙磺酸乙酯(EMS)、1,2,7,8 - 二环氧辛烷(DEO)、N - 甲基 - N'-硝基 - N - 亚硝基胍(MNNG)、2,3,5,6 - 四乙烯亚胺基 - 1,4 - 苯醌(TEB)和ICR - 170对修复缺陷菌株的毒性比对修复充足菌株的毒性更大。对于回复突变的诱导,N23 uvs - 2似乎比N23对MNNG和TEB以及高浓度的MMS和DEO更敏感,而N24对ICR - 170的敏感性比N24 uvs - 2高20倍。