摘要
利用基因枪法通过pTET-BI-Bar和pTATx-BN-Bin质粒分别将TetR和Barnase基因共转化粳稻品种台北309、4008S和籼稻品种D68。通过对R0代植株不同的基因进行PCR及Southern分析,结果表明,Barnase、TetR基因和控制Barnase基因的TA29-TX启动子均已整合到水稻基因组。其中,台北309和4008S分别获得了15株和6株阳性转基因植株,其外源基因转化率分别为4.5%和1.9%,其外源基因TetR和Barnase的共转化率分别为0.6%和0.3%。D68没有获得阳性转基因植株。
Taipei 309 (japonica), 4008S (japonica) and D68 (indica) were co-transformed with Barnase and TetR genes via the plasmids of pTET - BI - Bar and pTATx - BN - Bin by particle bombardment. The PCR and southern blot analyses of each gene in R0 plants showed that the Barnase, TetR genes and TA29 - TX promoter were successfully integrated into the genome of transgenic plants. 6 and 15 transgenic plants of 4008S and Taipei 309 were obtained, respectively. The gene transformation frequency of 4008S and Taipei 309 were 1.9 % and 4.5 %, respectively, and the efficiency of co-transformation of both TetR and Barnase genes of 4008S and Taipei 309 were 0. 3 % and 0.6 %, respectively. However, no transgenic plants were found in the indica variety D68.
出处
《杂交水稻》
CSCD
北大核心
2006年第5期59-63,共5页
Hybrid Rice
基金
中国科学院知识创新工程重要方向项目(KZCX3-SW-434)
湖南省杰出青年基金(03JJY1004)
关键词
水稻
基因枪转化
四环素调控的雄性不育基因
rice
transformation by particle bombardment
tetracycline-conditioned male sterile gene