Martin-Ortigosa Susana, Trewyn Brian G, Wang Kan
Department of Agronomy, Iowa State University, Ames, IA, 50011-1010, USA.
Center for Plant Transformation, Plant Sciences Institute, Iowa State University, Ames, IA, 50011-1010, USA.
Methods Mol Biol. 2017;1642:169-180. doi: 10.1007/978-1-4939-7169-5_11.
We describe a non-DNA-based system for delivering Cre recombinase protein into maize tissue using gold-plated mesoporous silica nanoparticle (Au-MSN). Cre protein is first loaded into the pores of Au-MSNs and then delivered using the biolistic method to immature embryos of a maize line (Lox-corn), which harbors loxP sites flanking a selection and a reporter gene. The release of the Cre recombinase protein inside the plant cell leads to recombination at the loxP sites, eliminating both genes. Visual screening is used to identify recombination events, which can be regenerated to mature and fertile plants. Using the experimental procedures and conditions described here, as high as 20% of bombarded embryos can produce regenerable recombinant callus events. This nanomaterial-mediated, DNA-free methodology has potential to become an effective tool for plant genome editing.
我们描述了一种基于非DNA的系统,该系统使用镀金介孔二氧化硅纳米颗粒(Au-MSN)将Cre重组酶蛋白递送至玉米组织中。首先将Cre蛋白装载到Au-MSN的孔中,然后使用生物弹道法将其递送至一个玉米品系(Lox-corn)的未成熟胚中,该品系在一个选择基因和一个报告基因两侧含有loxP位点。植物细胞内Cre重组酶蛋白的释放导致loxP位点处发生重组,从而消除这两个基因。通过视觉筛选来鉴定重组事件,这些事件可再生成成熟且可育的植株。使用此处描述的实验程序和条件,高达20%的轰击胚可产生可再生的重组愈伤组织事件。这种纳米材料介导的无DNA方法有潜力成为植物基因组编辑的有效工具。