Environ Health Perspect. 1978 Jun;24:113-6. doi: 10.1289/ehp.7824113.
In attempts to find a prescreen for mutagens that may induce heritable mutations in mammals, an in vivo somatic mutation test has been developed in the mouse that uses a localized gene product (hair pigment), is relatively fast and cheap, and gives results that have some predictive value for point mutation induction in spermatogonia. Embryos heterozygous at specific coat color loci are exposed to the presumptive mutagen, and 3 weeks later the fur is observed for spots of altered color. It is possible to distinguish spots resulting from expression of the recessive (RS's) from spots having various other causes.In tests with seven compounds, mutation rates per locus and unit dose have been calculated on the assumption that 175 cells are at risk per 10(1/4)-day embryo (a number derived from distribution of spot proportions). These rates are found to be roughly parallel to, but uniformly higher than spermatogonial point-mutation rates for the same seven compounds. The higher somatic rates are presumably due to the fact that RS's can result from several genetic mechanisms besides point mutations. The spot test, which has not to date given any false negatives, may thus be considered a useful in vivo prescreen for heritable germinal mutations in mammals.
为了寻找可能在哺乳动物中诱导遗传突变的诱变剂的预筛,在老鼠中开发了一种体内体细胞突变测试,该测试使用局部基因产物(毛发色素),相对快速且廉价,并提供了一些预测精原细胞点突变诱导的结果。在特定毛色基因座杂合的胚胎中暴露于推定的诱变剂,3 周后观察皮毛中颜色改变的斑点。可以区分由于隐性表达(RS)产生的斑点和具有各种其他原因的斑点。在对七种化合物的测试中,每 locus 和单位剂量的突变率是根据每个 10(1/4)-天胚胎有 175 个细胞处于危险之中的假设来计算的(这个数字是从斑点比例分布中得出的)。这些速率与同一七种化合物的精原细胞点突变率大致平行,但均匀高于后者。较高的体细胞率可能是因为 RS 除了点突变之外还可以由几种遗传机制产生。到目前为止,该斑点测试尚未出现任何假阴性,因此可以被认为是哺乳动物遗传生殖突变的有用体内预筛。