Laboratory of Plant Breeding, Faculty of Agriculture, Tohoku University, 981, Sendai, Japan.
Plant Cell Rep. 1996 Jun;15(10):727-30. doi: 10.1007/BF00232216.
A reproducible system has been developed for the production of transgenic plants in indica rice using Agrobacterium-mediated gene transfer. Three-week-old scutella calli served as an excellent starting material. These were infected with an Agrobacterium tumefaciens strain EHA101 carrying a plasmid pIG121Hm containing genes for β-glucuronidase (GUS) and hygromycin resistnace (HygR). Hygromycin (50 mg/l) was used as a selectable agent. Inclusion of acetosyringone (50μM) in the Agrobacterium suspension and co-culture media proved to be indispensable for successful transformation. Transformation efficiency of Basmati 370 was 22% which was as high as reported in japonica rice and dicots. A large number of morphologically normal, fertile transgenic plants were obtained. Integration of foreign genes into the genome of transgenic plants was confirmed by Southern blot analysis. GUS and HygR genes were inherited and expressed in R1 progeny. Mendelian segregation was observed in some R1 progeny.
已开发出一种可重现的系统,用于通过农杆菌介导的基因转移在籼稻中生产转基因植物。3 周龄的盾片愈伤组织可作为极好的起始材料。将其用携带质粒 pIG121Hm 的农杆菌菌株 EHA101 感染,该质粒含有β-葡萄糖醛酸酶(GUS)和潮霉素抗性(HygR)基因。潮霉素(50mg/L)用作选择性试剂。在农杆菌悬浮液和共培养培养基中添加乙酰丁香酮(50μM)被证明对成功转化是必不可少的。Basmati 370 的转化率为 22%,与报道的粳稻和双子叶植物一样高。获得了大量形态正常、可育的转基因植物。通过 Southern blot 分析证实了外源基因整合到转基因植物的基因组中。GUS 和 HygR 基因在 R1 代中遗传和表达。在一些 R1 代中观察到孟德尔分离。