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通过胚胎 TALEN mRNA 显微注射生成靶向小鼠突变体。

Generation of targeted mouse mutants by embryo microinjection of TALEN mRNA.

机构信息

Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Munich, Germany.

出版信息

Nat Protoc. 2013 Dec;8(12):2355-79. doi: 10.1038/nprot.2013.142. Epub 2013 Oct 31.

Abstract

Genetically engineered mice are instrumental for the analysis of mammalian gene function in health and disease. As classical gene targeting, which is performed in embryonic stem (ES) cell cultures and generates chimeric mice, is a time-consuming and labor-intensive procedure, we recently used transcription activator-like (TAL) effector nucleases (TALENs) for mutagenesis of the mouse genome directly in one-cell embryos. Here we describe a stepwise protocol for the generation of knock-in and knockout mice, including the selection of TALEN-binding sites, the design and construction of TALEN coding regions and of mutagenic oligodeoxynucleotides (ODNs) and targeting vectors, mRNA production, embryo microinjection and the identification of modified alleles in founder mutants and their progeny. After a setup time of 2-3 weeks of hands-on work for TALEN construction, investigators can obtain first founder mutants for genes of choice within 7 weeks after embryo microinjections.

摘要

基因工程小鼠是分析哺乳动物基因在健康和疾病中的功能的重要工具。由于经典的基因靶向技术是在胚胎干细胞(ES)培养物中进行的,并且会产生嵌合小鼠,因此该技术耗时且劳动强度大,我们最近使用转录激活子样效应物核酸酶(TALENs)直接在单细胞胚胎中对小鼠基因组进行诱变。本文描述了一种逐步的方案,用于生成敲入和敲除小鼠,包括 TALEN 结合位点的选择、TALEN 编码区以及诱变寡脱氧核苷酸(ODN)和靶向载体的设计和构建、mRNA 的产生、胚胎显微注射以及在起始突变体及其后代中鉴定修饰的等位基因。在进行 TALEN 构建的实际操作 2-3 周后,研究人员可以在胚胎显微注射后 7 周内获得首选基因的第一个起始突变体。

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