Thole Vera, Worland Barbara, Snape John W, Vain Philippe
Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Plant Physiol. 2007 Dec;145(4):1211-9. doi: 10.1104/pp.107.108563. Epub 2007 Oct 11.
The development of novel transformation vectors is essential to the improvement of plant transformation technologies. Here, we report the construction and testing of a new multifunctional dual binary vector system, pCLEAN, for Agrobacterium-mediated plant transformation. The pCLEAN vectors are based on the widely used pGreen/pSoup system and the pCLEAN-G/pCLEAN-S plasmids are fully compatible with the existing pGreen/pSoup vectors. A single Agrobacterium can harbor (1) pCLEAN-G and pSoup, (2) pGreen and pCLEAN-S, or (3) pCLEAN-G and pCLEAN-S vector combination. pCLEAN vectors have been designed to enable the delivery of multiple transgenes from distinct T-DNAs and/or vector backbone sequences while minimizing the insertion of superfluous DNA sequences into the plant nuclear genome as well as facilitating the production of marker-free plants. pCLEAN vectors contain a minimal T-DNA (102 nucleotides) consisting of direct border repeats surrounding a 52-nucleotide-long multiple cloning site, an optimized left-border sequence, a double left-border sequence, restriction sites outside the borders, and two independent T-DNAs. In addition, selectable and/or reporter genes have been inserted into the vector backbone sequence to allow either the counter-screening of backbone transfer or its exploitation for the production of marker-free plants. The efficiency of the different pCLEAN vectors has been assessed using transient and stable transformation assays in Nicotiana benthamiana and/or Oryza sativa.
新型转化载体的开发对于植物转化技术的改进至关重要。在此,我们报告了一种用于农杆菌介导的植物转化的新型多功能双元载体系统pCLEAN的构建与测试。pCLEAN载体基于广泛使用的pGreen/pSoup系统,并且pCLEAN-G/pCLEAN-S质粒与现有的pGreen/pSoup载体完全兼容。单个农杆菌可以携带(1)pCLEAN-G和pSoup,(2)pGreen和pCLEAN-S,或(3)pCLEAN-G和pCLEAN-S载体组合。pCLEAN载体的设计目的是能够从不同的T-DNA和/或载体骨架序列传递多个转基因,同时尽量减少多余DNA序列插入植物核基因组,并便于生产无标记植物。pCLEAN载体包含一个最小的T-DNA(102个核苷酸),由围绕一个52个核苷酸长的多克隆位点的直接边界重复序列、一个优化的左边界序列、一个双左边界序列、边界外的限制性酶切位点以及两个独立的T-DNA组成。此外,已将选择和/或报告基因插入载体骨架序列,以允许对骨架转移进行反筛选或利用其生产无标记植物。已使用本氏烟草和/或水稻中的瞬时和稳定转化试验评估了不同pCLEAN载体的效率。