突变
插入突变
同源重组
基因
突变体
基因靶向
清脆的
基因组编辑
遗传学
生物
突变
点突变
基因组
计算生物学
作者
Virginia E. Papaioannou,Richard R. Behringer
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory]
日期:2023-11-06
卷期号:2023 (12): pdb.over107956-pdb.over107956
被引量:2
标识
DOI:10.1101/pdb.over107956
摘要
The starting point in a mutational analysis of gene function is obtaining or producing a mutant. Here different methods of obtaining mouse mutants are discussed, including screening for spontaneous mutants, screening for mutants following chemical or X-ray mutagenesis, and producing mutations through targeted manipulation of the genome. Manipulation of the genome can be random, as in different types of insertional mutagenesis. Alternatively, targeted manipulation such as gene targeting using homologous recombination in embryonic stem (ES) cells or gene editing by CRISPR-Cas can be used to produce custom mutations in a specific gene. The basic methods are outlined, and the advantages and disadvantages of homologous recombination and CRISPR-Cas gene editing are discussed. Resources for obtaining mutations that already exist are provided. If, for your planned study, no suitable mutations are available, there is advice about what you should know about your gene of interest before embarking on a gene targeting experiment.
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