Storici Francesca, Resnick Michael A
Laboratory of Molecular Genetics, Chromosome Stability Section, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina, USA.
Methods Enzymol. 2006;409:329-45. doi: 10.1016/S0076-6879(05)09019-1.
In vivo genome manipulation through site-directed mutagenesis and chromosome rearrangements has been hindered by the difficulty in achieving high frequencies of targeting and the intensive labor required to create altered genomes that do not contain any heterologous sequence. Here we describe our approach, referred to as delitto perfetto, that combines the versatility of synthetic oligonucleotides for targeting with the practicality of a general selection system. It provides for an enormously wide variety of genome modifications via homologous recombination. Exceptional high frequencies of mutations are reached when a site-specific double-strand break (DSB) is induced within the locus targeted by the synthetic oligonucleotides. Presented in this chapter is an in-depth description of a series of applications of the delitto perfetto strategy for mutagenesis and chromosome modification both with and without the induction of a DSB, along with the procedures and materials.
通过定点诱变和染色体重排进行体内基因组操作一直受到阻碍,原因在于难以实现高靶向频率,以及创建不含任何异源序列的改变基因组需要大量人力。在此,我们描述了一种称为“完美诱变”的方法,该方法将合成寡核苷酸靶向的多功能性与通用筛选系统的实用性相结合。它通过同源重组实现了种类极为繁多的基因组修饰。当在合成寡核苷酸靶向的基因座内诱导位点特异性双链断裂(DSB)时,可达到异常高的突变频率。本章深入描述了“完美诱变”策略在有或没有诱导DSB情况下用于诱变和染色体修饰的一系列应用,以及相关程序和材料。