Bender E, Brendel M
Institut für Mikrobiologie, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Federal Republic of Germany.
Mutat Res. 1988 Jan;197(1):59-66. doi: 10.1016/0027-5107(88)90140-6.
dTMP exposure concentrations of 0.1 mM or higher are genotoxic in exponentially growing cells of thymidylate low-requiring mutants of Saccharomyces cerevisiae. Mutagenicity of excess dTMP is highest in an exposure concentration 10-fold of that needed for external supplementation of endogenously blocked thymidylate synthesis. Still higher dTMP concentrations are primarily cytotoxic. The canavanine forward-mutation system shows excess dTMP to be as potent a mutagen as irradiation by ultraviolet light. Mutagenicity of excess dTMP, however, differs from that of direct DNA-attacking mutagens in that it is highest in the absence of significant toxicity. Alkaline sucrose gradient centrifugation shows that excess dTMP does not induce significant numbers of DNA single- or double-strand breaks, while conditions of thymidylate deprivation lead to DNA-strand breaks and thymineless death.
在酿酒酵母胸苷酸低需求突变体的指数生长细胞中,0.1 mM或更高的dTMP暴露浓度具有遗传毒性。过量dTMP的致突变性在暴露浓度为内源性阻断胸苷酸合成所需浓度的10倍时最高。更高的dTMP浓度主要具有细胞毒性。刀豆氨酸正向突变系统显示,过量dTMP是一种与紫外线照射一样有效的诱变剂。然而,过量dTMP的致突变性与直接攻击DNA的诱变剂不同,因为它在没有明显毒性的情况下最高。碱性蔗糖梯度离心表明,过量dTMP不会诱导大量DNA单链或双链断裂,而胸苷酸剥夺条件会导致DNA链断裂和无胸腺死亡。