Tovkach Andriy, Zeevi Vardit, Tzfira Tzvi
Department of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI, USA.
Methods Mol Biol. 2010;649:315-36. doi: 10.1007/978-1-60761-753-2_20.
Zinc finger nucleases (ZFNs) can be designed to target virtually any long stretch of DNA sequence. Their expression in living cells has been shown to lead to gene targeting via homologous recombination, site-specific mutagenesis, and targeted DNA integration in various species. A variety of assays have been developed to test ZFN activity both in vitro and in vivo, and an assortment of vectors have been constructed to facilitate the analysis and expression of ZFNs in mammalian, and specifically human cells, as well as in other model organisms. Here we describe a set of protocols and vectors that were specifically designed to analyze ZFN activity in plant cells. Our assays provide the user with versatile tools and simple protocols for in-planta analysis of ZFN activity on transiently delivered and stably integrated mutated plant reporter (GUS)-encoding genes. Specifically designed for maximum compatibility with a generalized plant expression system, our vector system also allows easy assembly of ZFN plant transformation vectors for gene-targeting experiments in plants.
锌指核酸酶(ZFNs)能够被设计用于靶向几乎任何一段长的DNA序列。它们在活细胞中的表达已被证明可通过同源重组、位点特异性诱变以及在各种物种中的靶向DNA整合来实现基因靶向。已经开发了多种测定方法来在体外和体内测试ZFN活性,并且构建了各种各样的载体以促进ZFNs在哺乳动物细胞(特别是人类细胞)以及其他模式生物中的分析和表达。在这里,我们描述了一组专门设计用于分析植物细胞中ZFN活性的方案和载体。我们的测定为用户提供了通用工具和简单方案,用于在植物中对瞬时递送和稳定整合的突变植物报告基因(GUS)编码基因进行ZFN活性分析。我们的载体系统专门设计以与通用植物表达系统实现最大兼容性,还允许轻松组装用于植物基因靶向实验的ZFN植物转化载体。