Molecular Pathology Unit and Center for Cancer Research, Massachusetts General Hospital, Charlestown, Massachusetts, USA.
Nat Protoc. 2009;4(12):1855-67. doi: 10.1038/nprot.2009.209.
Zebrafish mutants have traditionally been obtained by using random mutagenesis or retroviral insertions, methods that cannot be targeted to a specific gene and require laborious gene mapping and sequencing. Recently, we and others have shown that customized zinc-finger nucleases (ZFNs) can introduce targeted frame-shift mutations with high efficiency, thereby enabling directed creation of zebrafish gene mutations. Here we describe a detailed protocol for constructing ZFN expression vectors, for generating and introducing ZFN-encoding RNAs into zebrafish embryos and for identifying ZFN-generated mutations in targeted genomic sites. All of our vectors and methods are compatible with previously described Zinc-Finger Consortium reagents for constructing engineered zinc-finger arrays. Using these methods, zebrafish founders carrying targeted mutations can be identified within 4 months.
斑马鱼突变体传统上是通过使用随机诱变或逆转录病毒插入获得的,这些方法不能针对特定基因,需要繁琐的基因定位和测序。最近,我们和其他人已经表明,定制的锌指核酸酶(ZFNs)可以高效地引入靶向移框突变,从而能够定向创建斑马鱼基因突变。在这里,我们描述了一个详细的方案,用于构建 ZFN 表达载体,生成和将 ZFN 编码的 RNA 导入斑马鱼胚胎,并鉴定靶向基因组位点的 ZFN 产生的突变。我们所有的载体和方法都与先前描述的用于构建工程化锌指阵列的 Zinc-Finger Consortium 试剂兼容。使用这些方法,可以在 4 个月内鉴定出携带靶向突变的斑马鱼种系。