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基于酶活性测定开发一种新的小鼠生化突变测试方法。II. 甲磺酸乙酯(EMS)的测试结果。

Development of a new biochemical mutation test in mice based upon measurement of enzyme activities. II. Test results with ethyl methanesulfonate (EMS).

作者信息

Bishop J B, Feurers R J

出版信息

Mutat Res. 1982 Aug;95(2-3):273-85. doi: 10.1016/0027-5107(82)90264-0.

Abstract

An experiment with ethyl methanesulfonate (EMS) was conducted to determine the feasibility of detecting chemically induced mutations in mice by quantitative analysis of metabolic characters using the test procedure of Feuers et al. (1982). A test population of 518 F1 mice from matings of untreated C57BL/6J females to C57BL/6J males treated with 0, 100, 175 or 200 mg/kg EMS was evaluated according to a set of multi-level biochemical and genetic screening criteria. The goal of the assay was identification of F1 individuals heterozygous at an unspecified locus for an induced mutant allele which altered the activity of one or more of 19 enzymes in brain and liver tissues of their F2 and F3 progeny, 8 individuals among a population of 345 F1's from the EMS-dosed groups were classified as confirmed mutants having at least 2 of their F2 progeny exhibiting the same enzyme aberrancy and transmitting this aberrancy to the F3 generation. No confirmed mutants were detected in the control population of 173 F1 individuals. These results indicate that this test method can be used to detect chemically induced mutations expressed as quantitative alterations in enzyme activity.

摘要

进行了一项使用甲磺酸乙酯(EMS)的实验,以确定通过采用Feuers等人(1982年)的测试程序对代谢特征进行定量分析来检测小鼠化学诱导突变的可行性。根据一组多级生化和遗传筛选标准,对来自未处理的C57BL/6J雌性与接受0、100、175或200mg/kg EMS处理的C57BL/6J雄性交配产生的518只F1小鼠的测试群体进行了评估。该检测的目标是鉴定在未指定位点杂合有诱导突变等位基因的F1个体,该突变等位基因改变了其F2和F3后代脑和肝组织中19种酶中一种或多种的活性,在来自EMS给药组的345只F1群体中,有8只个体被分类为已确认的突变体,其至少2只F2后代表现出相同的酶异常并将这种异常传递给F3代。在173只F1个体的对照群体中未检测到已确认的突变体。这些结果表明,该测试方法可用于检测以酶活性定量改变形式表达的化学诱导突变。

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