Many researchers have developed various methods for in-planta or floral dip transformation of Arabidopsis thaliana, one of the simple protocol and widely used to produce transgenic Arabidopsis. As the efficiency and e...Many researchers have developed various methods for in-planta or floral dip transformation of Arabidopsis thaliana, one of the simple protocol and widely used to produce transgenic Arabidopsis. As the efficiency and ease of getting a transformant is very much time consuming effort and less number of the transformants people get, we have developed a little modified transformation protocol to avoid the disparities. Four types of inoculums (inoculum1, inoculum2, inoculum3 and inoculum4) were used to check the transformation efficiency out of which Inoculum3 showed the highest rate of transformation among the four types. 0.07% Twin-20 also acts in same manner as silwet L-77 to increase the rate of transformation efficiency and glucose instead of sucrose can be used in inoculum to transform Arabidopsis. After vacuum infiltration keeping the Agrobacterium infected plants for 7-8 hrs horizontally in low light at 280C temperature condition, considered best to get an increased number of transformed seeds. Modified protocol produced ~12-14% increase in transformants. Selection pots (kanamycin supplemented soil filled pots) in place of selection plates (Kanamycin supplemented Murashige and Skoog agar plates) proved beneficial as no MS medium and no aseptic condition is required for selection of transformed plants. This increase in transformation efficiency consequently increased the percentage of homozygous and single copied stable transgenic lines.展开更多
DREB(dehydration responsive element binding)转录因子通过调控下游多个抗逆相关基因的表达,能有效提高植物的抗逆性。将构建的植物高效表达载体GmDREB::pCAMBIA1304,借助优化的floral-dip法,转入模式植物拟南芥,并经潮霉素Hygromycin...DREB(dehydration responsive element binding)转录因子通过调控下游多个抗逆相关基因的表达,能有效提高植物的抗逆性。将构建的植物高效表达载体GmDREB::pCAMBIA1304,借助优化的floral-dip法,转入模式植物拟南芥,并经潮霉素Hygromycine(40～50mg.L-1)抗性筛选得到22棵抗性植株。对抗性植株再进行PCR和GUS检测获得19颗阳性苗,阳性率为86.3%。对T1代种子进行抗性分离比例统计,有4个株系的分离比例接近3:1,符合孟德尔遗传定律,说明外源基因GmDREB在这些株系的染色体中可能是单拷贝插入。继续对上述4个株系的后代进行抗性筛选,现已得到2个纯合的转基因株系。导入的报告基因GUS组织染色检测表明,转入大豆DREB基因在拟南芥的根系和子叶中均有大量表达,并在叶脉中表达。展开更多
[ Objective] This study is aimed to transform gus gene into Chinese cabbage （Brassica rapa pekinensis） by floral-dip method. [ Method] The Chinese cabbage was transformed by floral-dip method for the first time. The...[ Objective] This study is aimed to transform gus gene into Chinese cabbage （Brassica rapa pekinensis） by floral-dip method. [ Method] The Chinese cabbage was transformed by floral-dip method for the first time. Then the cabbage seeds were harvested and screened by hygromycin, and the plants with resistance were confirmed by histochemical GUS assay and PCR detection. [ Result] The target gene was successfully integrated into the Chinese cabbage genome, and the transformation rate was 0.1%. [ Conclusion ] This study optimized the genetic transformation system for Chinese cabbage, and laid the foundation for improving the means of genetic transformation of Chinese cabbage.展开更多
文摘Many researchers have developed various methods for in-planta or floral dip transformation of Arabidopsis thaliana, one of the simple protocol and widely used to produce transgenic Arabidopsis. As the efficiency and ease of getting a transformant is very much time consuming effort and less number of the transformants people get, we have developed a little modified transformation protocol to avoid the disparities. Four types of inoculums (inoculum1, inoculum2, inoculum3 and inoculum4) were used to check the transformation efficiency out of which Inoculum3 showed the highest rate of transformation among the four types. 0.07% Twin-20 also acts in same manner as silwet L-77 to increase the rate of transformation efficiency and glucose instead of sucrose can be used in inoculum to transform Arabidopsis. After vacuum infiltration keeping the Agrobacterium infected plants for 7-8 hrs horizontally in low light at 280C temperature condition, considered best to get an increased number of transformed seeds. Modified protocol produced ~12-14% increase in transformants. Selection pots (kanamycin supplemented soil filled pots) in place of selection plates (Kanamycin supplemented Murashige and Skoog agar plates) proved beneficial as no MS medium and no aseptic condition is required for selection of transformed plants. This increase in transformation efficiency consequently increased the percentage of homozygous and single copied stable transgenic lines.
文摘DREB(dehydration responsive element binding)转录因子通过调控下游多个抗逆相关基因的表达,能有效提高植物的抗逆性。将构建的植物高效表达载体GmDREB::pCAMBIA1304,借助优化的floral-dip法,转入模式植物拟南芥,并经潮霉素Hygromycine(40～50mg.L-1)抗性筛选得到22棵抗性植株。对抗性植株再进行PCR和GUS检测获得19颗阳性苗,阳性率为86.3%。对T1代种子进行抗性分离比例统计,有4个株系的分离比例接近3:1,符合孟德尔遗传定律,说明外源基因GmDREB在这些株系的染色体中可能是单拷贝插入。继续对上述4个株系的后代进行抗性筛选,现已得到2个纯合的转基因株系。导入的报告基因GUS组织染色检测表明,转入大豆DREB基因在拟南芥的根系和子叶中均有大量表达,并在叶脉中表达。
基金Supported by Natural Science Foundation of Liaoning Province (901113)a Horizontal Project of Hangzhou Academy of Agricultural Sciences
文摘[ Objective] This study is aimed to transform gus gene into Chinese cabbage （Brassica rapa pekinensis） by floral-dip method. [ Method] The Chinese cabbage was transformed by floral-dip method for the first time. Then the cabbage seeds were harvested and screened by hygromycin, and the plants with resistance were confirmed by histochemical GUS assay and PCR detection. [ Result] The target gene was successfully integrated into the Chinese cabbage genome, and the transformation rate was 0.1%. [ Conclusion ] This study optimized the genetic transformation system for Chinese cabbage, and laid the foundation for improving the means of genetic transformation of Chinese cabbage.
