Institute of Molecular and Cell Biology, National University of Singapore, 10 Kent Ridge Crescent, 0511, Singapore, Republic of Singapore.
Plant Cell Rep. 1991 Sep;10(6-7):308-14. doi: 10.1007/BF00193148.
An efficient system for gene transfer into plants of Brassica juncea var. India Mustard, mediated by Agrobacterium tumefaciens. was developed through the manipulation of the culture medium and the use of the appropriate Agrobacterium strain. High frequency shoot regeneration (90-100%) was obtained from hypocotyl explants grown on medium containing 0.9% agarose, 3.3 mg/L AgNO3 and 0.5-2 mg/L BA in combination with 0.01-0.05 mg/L 2,4-D or 0.1-1 mg/L NAA. Of all the Agrobacterium strains tested, A. tumefaciens A208-SE, carrying the disarmed Ti plasmid and a binary vector pROA93, was the most effective for B. juncea transformation. pROA93 carries the coding sequences of the NPTII and the GUS genes, both driven by a common CaMV 35S promoter in two divergent directions. Inoculated explants grown on the selection medium in the presence of 0.5 mg/L BA and 0.1 mg/L NAA gave rise to transgenic shoots at the highest frequency (9%). All Ro transgenic plants were phenotypically normal, but variation in expression patterns of the GUS gene occurred among the transgenic plants in an organ- and tissue-specific manner. Both the NPTII and the GUS genes were transmitted to the R1 seed progeny and showed co-segregation.
利用农杆菌介导的高效基因转移系统将 Brassica juncea var. India Mustard 植物的基因转移。通过对培养基的操纵和适当的农杆菌菌株的使用来实现。从在含有 0.9%琼脂、3.3 mg/L AgNO3 和 0.5-2 mg/L BA 的培养基上生长的下胚轴外植体中获得了高频芽再生(90-100%),同时结合使用 0.01-0.05 mg/L 2,4-D 或 0.1-1 mg/L NAA。在所测试的所有农杆菌菌株中,携带无武装 Ti 质粒和二元载体 pROA93 的 A. tumefaciens A208-SE 对 B. juncea 转化最为有效。pROA93 携带 NPTII 和 GUS 基因的编码序列,均由一个共同的 CaMV 35S 启动子在两个相反的方向驱动。在含有 0.5 mg/L BA 和 0.1 mg/L NAA 的选择培养基上生长的接种外植体以最高频率(9%)产生转基因芽。所有 Ro 转基因植物表型均正常,但 GUS 基因的表达模式在转基因植物中存在器官和组织特异性的差异。NPTII 和 GUS 基因均传递给 R1 种子后代,并表现出共分离。