Sonti R V, Tissier A F, Wong D, Viret J F, Signer E R
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139-4307, USA.
Plant Mol Biol. 1995 Sep;28(6):1127-32. doi: 10.1007/BF00032673.
The coding sequence for FLP recombinase, originally from the 2 mu plasmid of Saccharomyces cerevisiae, was introduced into Arabidopsis behind the cauliflower mosaic virus 35S promoter. FLP activity was monitored by the glucuronidase activity resulting from inversion of an antisense-oriented GUS reporter gene flanked by a pair of FRT target sites in inverted repeat. FLP-dependent Gus activity was observed in both transient assays and transgenic plants. The FLP system will be useful for a variety of in planta genetic manipulations.
最初来自酿酒酵母2μm质粒的FLP重组酶编码序列,被导入拟南芥中花椰菜花叶病毒35S启动子的下游。通过反义方向的GUS报告基因(两侧为一对反向重复的FRT靶位点)的反向转化产生的葡糖醛酸酶活性来监测FLP活性。在瞬时试验和转基因植物中均观察到了FLP依赖性的Gus活性。FLP系统将有助于多种植物体内的基因操作。