Nishimura Kohei, Fukagawa Tatsuo
Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.
Chromosome Res. 2017 Oct;25(3-4):253-260. doi: 10.1007/s10577-017-9559-7. Epub 2017 Jun 6.
Generation of cells with a loss-of-function mutation in a gene (knockout cells) is a valuable technique for studying the function of a given gene product. However, if the product of the target gene is essential for cell viability, conditional knockout cell lines must be generated. Recently, as gene editing technology using CRISPR/Cas9 has developed, it has become possible to produce conditional knockout cell lines using this technique. However, to obtain final conditional knockout cell lines, it is necessary to perform several experiments with multiple complicated steps. In this paper, we introduce an easy and efficient method to generate conditional knockout cell lines based on combining auxin-inducible degron (AID) technology with CRISPR/Cas9 gene editing. Our method only requires performing a single transfection and is therefore an easy and rapid method to obtain a conditional knockout cell line.
产生某一基因功能缺失突变的细胞(基因敲除细胞)是研究特定基因产物功能的一项重要技术。然而,如果靶基因的产物对细胞生存力至关重要,就必须构建条件性基因敲除细胞系。近年来,随着使用CRISPR/Cas9的基因编辑技术的发展,利用该技术构建条件性基因敲除细胞系已成为可能。然而,要获得最终的条件性基因敲除细胞系,需要进行多个复杂步骤的多项实验。在本文中,我们介绍了一种简单高效的方法,即通过将生长素诱导降解子(AID)技术与CRISPR/Cas9基因编辑相结合来构建条件性基因敲除细胞系。我们的方法只需要进行一次转染,因此是一种获得条件性基因敲除细胞系的简便快速的方法。