Manjanatha Mugimane G, Cao Xuefei, Shelton Sharon D, Mittelstaedt Roberta A, Heflich Robert H
Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, USA.
Methods Mol Biol. 2013;1044:97-119. doi: 10.1007/978-1-62703-529-3_5.
Transgenic mutation assays are used to identify and characterize genotoxic hazards and for determining the mode of action for carcinogens. The three most popular transgenic mutational models are Big Blue® (rats or mice), Muta™ mouse (mice), and gpt-delta (rats or mice). The Big Blue® and Muta™ mouse models use the cII gene as a reporter of mutation whereas gpt-delta rodents use the gpt gene and the red/gam genes (Spi⁻ selection) as mutation reporter genes. Here we describe methodology for conducting mutation assays with these transgenes. Transgenes recovered from tissue DNA are packaged into infectious lambda phage, bacteria are infected with the phage, and cII-mutant and Spi⁻ plaques and gpt-mutant colonies are isolated using selective conditions and quantified. Selected mutants can be further analyzed for identification of small sequence alterations in the cII and gpt genes and large deletions at the Spi⁻ locus.
转基因突变分析用于识别和表征遗传毒性危害,并确定致癌物的作用模式。三种最常用的转基因突变模型是大蓝®(大鼠或小鼠)、诱变™小鼠(小鼠)和gpt-δ(大鼠或小鼠)。大蓝®和诱变™小鼠模型使用cII基因作为突变报告基因,而gpt-δ啮齿动物使用gpt基因和red/gam基因(Spi⁻选择)作为突变报告基因。在此,我们描述了使用这些转基因进行突变分析的方法。从组织DNA中回收的转基因被包装成有感染力的λ噬菌体,用该噬菌体感染细菌,并使用选择性条件分离cII突变体和Spi⁻噬菌斑以及gpt突变菌落并进行定量。可对选定的突变体进行进一步分析,以鉴定cII和gpt基因中的小序列改变以及Spi⁻位点的大缺失。