Nishimura Kohei, Fukagawa Tatsuo
Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan.
Graduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Bio Protoc. 2021 Jul 20;11(14):e4092. doi: 10.21769/BioProtoc.4092.
Inducing loss of function of a target protein using methods such as gene knockout is a powerful and useful strategy for analyzing protein function in cells. In recent years, the CRISPR/Cas-9-based gene knockout technology has been widely used across a variety of eukaryotes; however, this type of simple gene knockout strategy is not applicable to essential genes, which require a conditional knockout system. The auxin-inducible degron (AID) system enables rapid depletion of the target protein in an auxin-dependent manner and has been used to generate conditional mutants in various eukaryotic cell lines. One problem with the AID system is the use of high auxin concentrations for protein degradation, which can cause cytotoxicity. Recently, we established a super-sensitive AID (ssAID) system that allowed a reduction in the amount of auxin required by more than 1,000-fold. We also utilized a single-step method to generate AID-based conditional knockout cells with a ssAID system in various cell lines. In this protocol, we introduce our improved method, which provides a powerful tool for the investigation of the roles of essential genes.
使用基因敲除等方法诱导靶蛋白功能丧失是分析细胞中蛋白质功能的一种强大且有用的策略。近年来,基于CRISPR/Cas-9的基因敲除技术已在多种真核生物中广泛应用;然而,这种简单的基因敲除策略不适用于必需基因,必需基因需要一个条件性敲除系统。生长素诱导降解子(AID)系统能够以生长素依赖的方式快速耗尽靶蛋白,并已用于在各种真核细胞系中产生条件性突变体。AID系统的一个问题是使用高浓度生长素进行蛋白质降解,这可能会导致细胞毒性。最近,我们建立了一种超灵敏AID(ssAID)系统,该系统可将所需生长素的量减少1000倍以上。我们还利用一种单步方法,在各种细胞系中用ssAID系统生成基于AID的条件性敲除细胞。在本方案中,我们介绍了我们改进的方法,该方法为研究必需基因的作用提供了一个强大的工具。