Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526, Japan.
Genes Cells. 2013 Apr;18(4):315-26. doi: 10.1111/gtc.12037. Epub 2013 Feb 6.
Transcription activator-like effector nucleases (TALENs) have recently arisen as effective tools for targeted genome engineering. Here, we report streamlined methods for the construction and evaluation of TALENs based on the 'Golden Gate TALEN and TAL Effector Kit' (Addgene). We diminished array vector requirements and increased assembly rates using six-module concatemerization. We altered the architecture of the native TALEN protein to increase nuclease activity and replaced the final destination vector with a mammalian expression/in vitro transcription vector bearing both CMV and T7 promoters. Using our methods, the whole process, from initiating construction to completing evaluation directly in mammalian cells, requires only 1 week. Furthermore, TALENs constructed in this manner may be directly applied to transfection of cultured cells or mRNA synthesis for use in animals and embryos. In this article, we show genomic modification of HEK293T cells, human induced pluripotent stem cells, Drosophila melanogaster, Danio rerio and Xenopus laevis, using custom-made TALENs constructed and evaluated with our protocol. Our methods are more time efficient compared with conventional yeast-based evaluation methods and provide a more accessible and effective protocol for the application of TALENs in various model organisms.
转录激活因子样效应物核酸酶(TALENs)最近已成为靶向基因组工程的有效工具。在这里,我们报告了基于“Golden Gate TALEN 和 TAL 效应物试剂盒”(Addgene)构建和评估 TALENs 的简化方法。我们通过六模块串联减少了数组载体的要求并提高了组装速度。我们改变了天然 TALEN 蛋白的结构以提高核酸酶活性,并将最终目的载体替换为带有 CMV 和 T7 启动子的哺乳动物表达/体外转录载体。使用我们的方法,从开始构建到直接在哺乳动物细胞中完成评估的整个过程仅需 1 周。此外,以这种方式构建的 TALENs 可直接用于转染培养的细胞或用于动物和胚胎的 mRNA 合成。在本文中,我们展示了使用我们的方案构建和评估的定制 TALENs 对 HEK293T 细胞、人诱导多能干细胞、果蝇、斑马鱼和爪蟾进行基因组修饰。与传统的基于酵母的评估方法相比,我们的方法更节省时间,为 TALENs 在各种模式生物中的应用提供了更便捷有效的方案。