Vlasakova Katerina, Skopek Thomas R, Glaab Warren E
Molecular and Investigative Toxicology, Merck Research Laboratories, WP45-320, West Point, PA 19486, USA.
Mutat Res. 2005 Oct 15;578(1-2):225-37. doi: 10.1016/j.mrfmmm.2005.05.022.
A novel forward mutation assay has been developed in Salmonella typhimurium based on resistance to 5-fluorouracil (FU). The mutational target in the FU assay was determined to be the uracil phosphoribosyl transferase (upp) gene. To validate the upp gene as a suitable target for monitoring a variety of induced mutations, the mutational specificity was determined for five mechanistically different mutagens. The mutagens included a polycyclic hydrocarbon (benzo[a]pyrene, B[a]P), SN1 and SN2 alkylating agents (N-nitroso-N-methylurea, MNU, and methyl methanesulfonate, MMS, respectively), a frameshift mutagen (ICR-191), and an oxidative-damaging agent (hydrogen peroxide, H2O2). Induced mutation frequencies were measured in the presence and absence of the plasmid pKM101 (strain FU100 and FU1535, respectively). pKM101 renders FU100 more susceptible to induced mutation by providing error-prone replicative bypass of DNA adducts. B[a]P, MMS, and H2O2 failed to induce the mutant frequency in FU1535, demonstrating the dependence of pKM101 on induced mutations with these agents. ICR-191 and MNU were not dependent on pKM101, and did significantly induce mutations in FU1535. In contrast to FU1535, all agents significantly induced mutations in FU100. Approximately 60 independent mutants were sequenced for each agent that significantly induced the mutant frequency above background. The resulting mutational spectra illustrated predictable molecular fingerprints based on known mutagenic mechanisms for each agent. The predominant mutations observed were G:C to T:A transversions for B[a]P, A:T to T:A and G:C to T:A transversions for MMS, G:C to T:A transversions and A:T frameshifts for H2O2, G:C frameshifts for ICR-191, and G:C to A:T transitions for MNU. It can be concluded that the upp gene in the FU assay is a sensitive and suitable target to monitor a variety of induced mutations in Salmonella.
基于对5-氟尿嘧啶(FU)的抗性,在鼠伤寒沙门氏菌中开发了一种新型的正向突变试验。FU试验中的突变靶点被确定为尿嘧啶磷酸核糖转移酶(upp)基因。为了验证upp基因作为监测各种诱导突变的合适靶点,测定了五种机制不同的诱变剂的突变特异性。这些诱变剂包括多环烃(苯并[a]芘,B[a]P)、SN1和SN2烷基化剂(分别为N-亚硝基-N-甲基脲,MNU,和甲基磺酸甲酯,MMS)、移码诱变剂(ICR-191)和氧化损伤剂(过氧化氢,H2O2)。在存在和不存在质粒pKM101的情况下(分别为FU100和FU1535菌株)测量诱导突变频率。pKM101通过提供易出错的DNA加合物复制旁路,使FU100对诱导突变更敏感。B[a]P、MMS和H2O2未能在FU1535中诱导突变频率,表明pKM101对这些试剂诱导突变的依赖性。ICR-191和MNU不依赖于pKM101,并且在FU1535中确实显著诱导了突变。与FU1535相反,所有试剂在FU100中均显著诱导了突变。对于每种显著诱导突变频率高于背景的试剂,对大约60个独立突变体进行了测序。所得的突变谱基于每种试剂已知的诱变机制显示出可预测的分子指纹。观察到的主要突变是B[a]P的G:C到T:A颠换、MMS的A:T到T:A和G:C到T:A颠换、H2O2的G:C到T:A颠换和A:T移码、ICR-191的G:C移码以及MNU的G:C到A:T转换。可以得出结论,FU试验中的upp基因是监测鼠伤寒沙门氏菌中各种诱导突变的敏感且合适的靶点。