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用于在小鼠和人类细胞中进行双等位基因条件性和可逆基因敲除的FLIP和FLIP-FlpE靶向载体的构建

Generation of FLIP and FLIP-FlpE Targeting Vectors for Biallelic Conditional and Reversible Gene Knockouts in Mouse and Human Cells.

作者信息

Koo Bon-Kyoung

机构信息

IMBA Institute of Molecular Biotechnology, Stem Cells and Organoids, Vienna, Austria.

出版信息

Methods Mol Biol. 2018;1842:255-264. doi: 10.1007/978-1-4939-8697-2_19.

Abstract

Rapid generation of conditional knockout models in a diploid system is challenging. Recently, CRISPR-FLIP strategy has been introduced, which facilitates the generation of biallelic conditional or reversible gene knockouts in various mammalian cell lines including mouse and human pluripotent stem cells by codelivery of the CRISPR/Cas9 system and a universal intronic cassette-FLIP and FLIP-FlpE. Here, I describe the design and cloning method of FLIP and FLIP-FlpE targeting vectors for conditional and reversible gene knockouts. This method is applicable to mouse embryonic stem cells, human induced pluripotent stem cells, and adult stem cell-derived organoids.

摘要

在二倍体系统中快速生成条件性基因敲除模型具有挑战性。最近,引入了CRISPR-FLIP策略,该策略通过共递送CRISPR/Cas9系统和一个通用内含子盒-FLIP以及FLIP-FlpE,促进在包括小鼠和人类多能干细胞在内的各种哺乳动物细胞系中生成双等位基因条件性或可逆性基因敲除。在此,我描述了用于条件性和可逆性基因敲除的FLIP和FLIP-FlpE靶向载体的设计和克隆方法。该方法适用于小鼠胚胎干细胞、人类诱导多能干细胞以及成体干细胞来源的类器官。

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