Masui Shinji, Shimosato Daisuke, Toyooka Yayoi, Yagi Rika, Takahashi Kazue, Niwa Hitoshi
Laboratory for Pluripotent Cell Studies, RIKEN Center for Developmental Biology Minatojima-minamimachi 2-2-3, Kobe, Japan.
Nucleic Acids Res. 2005 Mar 1;33(4):e43. doi: 10.1093/nar/gni043.
The growing use of mouse embryonic stem (ES) cells in research emphasizes their importance in studies of molecular mechanisms that maintain pluripotency and direct cellular differentiation. Although systems for regulatable transgene expression are essential for fine analysis of cellular processes at the molecular level, a strategy for the establishment of multiple ES cell lines carrying any of these systems has not yet been described. Here, we report our development of the ROSA-TET system, an effective system for the establishment of multiple ES cell lines carrying a tetracycline (Tc)-regulatable transgene at the Gt (ROSA)26asSor (ROSA26) locus. This system contains a knock-in step of a construct carrying both loxP and its mutant sequences into the ROSA26 locus, followed by a subsequent exchange step that introduces a cDNA to be Tc-regulated to the locus using the recombinase-mediated cassette exchange reaction. Both steps are demonstrated to give desired clones with high efficiency, suggesting that this system can be introduced readily into any ES cell lines, leading to the simultaneous establishment of multiple cell lines carrying different Tc-regulated cDNAs. We believe that use of this system will strongly accelerate molecular biological research using ES cells.
小鼠胚胎干细胞(ES细胞)在研究中的应用日益广泛,这凸显了它们在维持多能性和指导细胞分化的分子机制研究中的重要性。尽管可调控转基因表达系统对于在分子水平上精细分析细胞过程至关重要,但尚未有关于建立携带任何此类系统的多个ES细胞系的策略的描述。在此,我们报告了ROSA-TET系统的开发,这是一种用于在Gt(ROSA)26asSor(ROSA26)位点建立携带四环素(Tc)可调控转基因的多个ES细胞系的有效系统。该系统包括将携带loxP及其突变序列的构建体敲入ROSA26位点的步骤,随后是一个交换步骤,该步骤使用重组酶介导的盒式交换反应将待Tc调控的cDNA引入该位点。这两个步骤均被证明能高效产生所需克隆,表明该系统可轻松引入任何ES细胞系,从而同时建立携带不同Tc调控cDNA的多个细胞系。我们相信,该系统的使用将有力地加速利用ES细胞进行的分子生物学研究。