Ehling U H
Arch Toxicol. 1977 Sep 21;38(1-2):1-11. doi: 10.1007/BF00293658.
Dominant lethal mutations are due to chromosome aberrations as demonstrated by analysis of first cleavage. With a sample size of 40-45 mice per dose the induction of dominant lethal mutations by 10 mg/kg of methyl methanesulfonat (MMS) can be detected in spermatids in the mating interval 9-12 days posttreatment (6-11%). In the same mating interval a dose of 150 mg/kg of MMS induces 100% dominant lethal mutations. MMS and other chemical mutagens can be characterized by their different spermatogenic response. The germ cell stage specific induction of dominant lethal mutations by chemical agents is very likely due to their different pathways and therefore, to different effects on the structural and macromolecular changes during spermatogenesis. The feasibility of standardizing test protocol for the dominant lethal assay in mice, based on collaborative studies, is discussed. The reproducibility of results and the sensitivity of the induction of dominant lethal mutations in the collaborative studies demonstrate the usefullness of the method for mutagenicity screening.
显性致死突变是由染色体畸变引起的,首次卵裂分析证明了这一点。每剂量使用40 - 45只小鼠作为样本,10毫克/千克的甲基磺酸甲酯(MMS)在处理后9 - 12天的交配间隔期可在精子细胞中检测到显性致死突变的诱导(6 - 11%)。在相同的交配间隔期,150毫克/千克的MMS剂量可诱导100%的显性致死突变。MMS和其他化学诱变剂可通过其不同的生精反应来表征。化学试剂对显性致死突变的生殖细胞阶段特异性诱导很可能是由于它们不同的途径,因此,对精子发生过程中的结构和大分子变化有不同的影响。基于合作研究,讨论了标准化小鼠显性致死试验方案的可行性。合作研究中结果的可重复性和显性致死突变诱导的敏感性证明了该方法用于致突变性筛选的实用性。