INSERM, U643, 44093, Nantes, France.
Transgenic Res. 2010 Jun;19(3):363-71. doi: 10.1007/s11248-009-9323-7. Epub 2009 Sep 26.
The generation of genetically modified animals or plants with gene-targeted deletions or modifications is a powerful tool to analyze gene function, study disease and produce organisms of economical interest. Until recently, the generation of animals with gene targeted manipulations has been accomplished by homologous recombination (HR) in embryonic stem (ES) cells or cloning through nuclear transfer and has been limited to a few species. Recently, a new technology based on the use of gene-targeted zinc-finger nucleases (ZFNs) was developed and used for the generation of organisms with gene-targeted deletions and/or modifications when combined with HR. ZFNs have been used to generate modified organisms such as plants, Drosophila, zebra fish and rats with gene-targeted mutations. This perspective manuscript is a short review on the use of ZFNs for the genetic engineering of plants and animals, with particular emphasis on our recent work involving rats. We also discuss the application of other targeted nucleases, including homing endonucleases. Microinjection of plasmid or mRNA for ZFNs into rat embryos allowed targeted, rapid, complete, permanent and heritable disruption of endogenous loci. The application of ZFNs to generate gene-targeted knockouts in species where ES cells or cloning techniques are not available is an important new development to answer fundamental biological questions and develop models of economical interest such as for the production of humanized antibodies. Further refinements of ZFN technology in combination with HR may allow knock-ins in early embryos even in species where ES cells or cloning techniques are available.
利用基因靶向缺失或修饰技术生成转基因动植物是分析基因功能、研究疾病和生产经济利益生物体的有力工具。直到最近,通过同源重组(HR)在胚胎干细胞(ES 细胞)或核转移克隆中对动物进行基因靶向操作的生成一直局限于少数几种物种。最近,一种基于使用基因靶向锌指核酸酶(ZFNs)的新技术得到了发展,并与 HR 结合用于生成基因靶向缺失和/或修饰的生物体。ZFNs 已被用于生成具有基因靶向突变的改良生物体,如植物、果蝇、斑马鱼和大鼠。本文简要综述了 ZFN 用于动植物的遗传工程,特别强调了我们最近涉及大鼠的工作。我们还讨论了其他靶向核酸酶的应用,包括归巢内切核酸酶。将 ZFN 的质粒或 mRNA 微注射到大鼠胚胎中,可以靶向、快速、完全、永久和可遗传地破坏内源性基因座。在 ES 细胞或克隆技术不可用的物种中,利用 ZFN 生成基因靶向敲除体是一个重要的新发展,可以回答基础生物学问题并开发具有经济利益的模型,例如生产人源化抗体。与 HR 结合进一步改进 ZFN 技术,甚至可能允许在 ES 细胞或克隆技术可用的物种中进行早期胚胎的基因敲入。