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用于基因功能分析的小鼠胚胎干细胞中的多基因转移和一体化条件性敲除系统

Multiple Gene Transfer and All-In-One Conditional Knockout Systems in Mouse Embryonic Stem Cells for Analysis of Gene Function.

作者信息

Suzuki Teruhiko, Takagi Satoko, Hara Takahiko

机构信息

Stem Cell Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Front Cell Dev Biol. 2022 Mar 28;10:870629. doi: 10.3389/fcell.2022.870629. eCollection 2022.

Abstract

Mouse embryonic stem cells (ESCs) are powerful tools for functional analysis of stem cell-related genes; however, complex gene manipulations, such as locus-targeted introduction of multiple genes and conditional gene knockout conditional knockout, are technically difficult. Here, we review recent advances in technologies aimed at generating cKO clones in ESCs, including two new methods developed in our laboratory: the simultaneous or sequential integration of multiple genes system for introducing an unlimited number of gene cassettes into a specific chromosomal locus using reciprocal recombinases; and the all-in-one cKO system, which enables introduction of an EGFP reporter expression cassette and FLAG-tagged gene of interest under an endogenous promoter. In addition, methods developed in other laboratories, including conventional approaches to establishment of cKO cell clones, inducible Cas9-mediated cKO generation, and cKO assisted by reporter construct, invertible gene-trap cassette, and conditional protein degradation. Finally, we discuss the advantages of each approach, as well as the remaining issues and challenges.

摘要

小鼠胚胎干细胞(ESCs)是用于干细胞相关基因功能分析的强大工具;然而,复杂的基因操作,如多个基因的位点靶向导入和条件性基因敲除,在技术上具有难度。在此,我们综述了旨在在胚胎干细胞中产生条件性敲除(cKO)克隆的技术的最新进展,包括我们实验室开发的两种新方法:使用相互重组酶将无限数量的基因盒引入特定染色体位点的多个基因系统的同时或顺序整合;以及一体化cKO系统,该系统能够在内源启动子下引入增强绿色荧光蛋白(EGFP)报告基因表达盒和带有FLAG标签的目的基因。此外,还介绍了其他实验室开发的方法,包括建立cKO细胞克隆的传统方法、诱导型Cas9介导的cKO产生,以及由报告基因构建体、可逆基因捕获盒和条件性蛋白质降解辅助的cKO。最后,我们讨论了每种方法的优点,以及剩余的问题和挑战。

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