Department of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Methods. 2011 Apr;53(4):339-46. doi: 10.1016/j.ymeth.2010.12.019. Epub 2010 Dec 23.
Zinc-finger nucleases (ZFNs) are designer nucleases capable of cleaving a prespecified target DNA within complex genomes. ZFNs consist of a non-specific endonuclease domain fused to an engineered DNA-binding domain that tethers the nuclease activity to the chosen chromosomal site. The endonuclease-induced DNA double strand break triggers a cellular DNA damage response, resulting in double strand break repair by either accurate homologous recombination (HR) or error-prone non-homologous end-joining (NHEJ). Thus, ZFNs are powerful tools for targeted genome engineering in a variety of mammalian cell types, including embryonic (ESCs) and induced pluripotent stem cells (iPSCs). As a paradigm for genome editing in pluripotent stem cells, we describe the use of ZFNs in murine ESCs for generating knockout alleles by NHEJ without selection or by HR employing different selection schemes.
锌指核酸酶(ZFNs)是一种设计性核酸酶,能够在复杂的基因组中切割预定的靶标 DNA。ZFNs 由非特异性内切酶结构域与工程化的 DNA 结合结构域融合而成,将核酸酶活性连接到选定的染色体位置。内切酶诱导的 DNA 双链断裂引发细胞 DNA 损伤反应,导致双链断裂修复通过精确的同源重组(HR)或易错的非同源末端连接(NHEJ)。因此,ZFNs 是在多种哺乳动物细胞类型中进行靶向基因组工程的有力工具,包括胚胎干细胞(ESCs)和诱导多能干细胞(iPSCs)。作为多能干细胞中基因组编辑的范例,我们描述了在小鼠 ESCs 中使用 ZFNs 通过 NHEJ 产生无选择的敲除等位基因,或通过 HR 采用不同的选择方案。