Stem Cell and Developmental Biology Department, Genome Institute of Singapore, 60 Biopolis Street, Singapore, 138672, Singapore,
Biotechnol Lett. 2013 Dec;35(12):1991-6. doi: 10.1007/s10529-013-1303-6. Epub 2013 Aug 2.
Traditionally, conditional knockout studies in mouse have utilized the Cre or Flpe technology to activate the expression of reporter genes such as lacZ or PLAP. Employing these reporter genes, however, requires tissue fixation. To make way for downstream in vivo or in vitro applications, we have inserted enhanced green fluorescent protein (EGFP) into the endogenous Sox9 locus and generated a novel conditional Sox9 null allele, by flanking the entire Sox9 coding region with loxP sites and inserting an EGFP reporter gene into the 3'-UTR allowing for EGFP to be expressed upon Sox9 loss of function yet under the control of the endogenous Sox9 promoter. Mating this new allele to any Cre-expressing line, the fate of Sox9 null cells can be traced in the cell type of interest in vivo or in vitro after fluorescence-activated cell sorting.
传统上,在小鼠中进行条件性基因敲除研究利用 Cre 或 Flpe 技术激活报告基因如 lacZ 或 PLAP 的表达。然而,使用这些报告基因需要组织固定。为了给下游的体内或体外应用让路,我们将增强型绿色荧光蛋白(EGFP)插入到内源性 Sox9 基因座中,并通过loxP 位点侧翼包围整个 Sox9 编码区,将 EGFP 报告基因插入 3'-UTR,使 EGFP 在 Sox9 功能丧失时表达,但受内源性 Sox9 启动子的控制,从而产生了一种新型的条件性 Sox9 缺失等位基因。将这个新的等位基因与任何表达 Cre 的系交配,在体内或体外通过荧光激活细胞分选后, Sox9 缺失细胞的命运可以在感兴趣的细胞类型中被追踪。