The Lambda Select cII Mutation Detection System

被引:3
作者
Besaratinia, Ahmad [1 ]
Tommasi, Stella [1 ]
机构
[1] Univ Southern Calif, Dept Prevent Med, USC Keck Sch Med, Los Angeles, CA 90089 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2018年 / 134期
基金
美国国家卫生研究院;
关键词
Immunology and Infection; Issue; 134; Bacteriophage; cII Transgene; Embryonic Mouse Fibroblasts; EMF; Mutation; Shuttle Vector; ETHYLNITROSOUREA-INDUCED MUTATION; ENDOGENOUS HPRT GENE; BIG BLUE(R) MOUSE; IN-VIVO-CII; TRANSGENIC MICE; MUTANT FREQUENCY; LACL TRANSGENE; DNA-ADDUCTS; MUTAGENIC RESPONSE; SOMATIC MUTATIONS;
D O I
10.3791/57510
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A number of transgenic animal models and mutation detection systems have been developed for mutagenicity testing of carcinogens in mammalian cells. Of these, transgenic mice and the Lambda (lambda) Select cII Mutation Detection System have been employed for mutagenicity experiments by many research groups worldwide. Here, we describe a detailed protocol for the Lambda Select cII mutation assay, which can be applied to cultured cells of transgenic mice/rats or the corresponding animals treated with a chemical/physical agent of interest. The protocol consists of the following steps: (1) isolation of genomic DNA from the cells or organs/tissues of transgenic animals treated in vitro or in vivo, respectively, with a test compound; (2) recovery of the lambda shuttle vector carrying a mutational reporter gene (i.e., cII transgene) from the genomic DNA; (3) packaging of the rescued vectors into infectious bacteriophages; (4) infecting a host bacteria and culturing under selective conditions to allow propagation of the induced cII mutations; and (5) scoring the cII-mutants and DNA sequence analysis to determine the cII mutant frequency and mutation spectrum, respectively.
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页数:10
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