Zakharchenko N S, Rukavtsova E B, Gudkov A T, Bur'ianov Ia I
Genetika. 2005 Nov;41(11):1445-52.
Plasmids with a synthetic gene of the mammalian antimicrobial peptide cecropin P1 (cecP1) controlled by the constitutive promoter 35S RNA of cauliflower mosaic virus were constructed. Agrobacterial transformation of tobacco plants was conducted using the obtained recombinant binary vector. The presence of gene cecP1 in the plant genome was confirmed by PCR. The expression of gene cecP1 in transgenic plants was shown by Northern blot analysis. The obtained transgenic plants exhibit enhanced resistance to phytopathogenic bacteria Pseudomonas syringae, P. marginata, and Erwinia carotovora. The ability of transgenic plants to express cecropin P1 was transmitted to the progeny. F1 and F2 plants had the normal phenotype (except for a changed coloration of flowers) and retained the ability to produce normal viable seeds upon self-pollination. Lines of F1 plants with Mendelian segregation of transgenic traits were selected.
构建了含有受花椰菜花叶病毒组成型启动子35S RNA控制的哺乳动物抗菌肽天蚕素P1(cecP1)合成基因的质粒。使用获得的重组二元载体对烟草植株进行农杆菌转化。通过PCR确认植物基因组中cecP1基因的存在。通过Northern印迹分析显示转基因植物中cecP1基因的表达。所获得的转基因植物对植物病原菌丁香假单胞菌、边缘假单胞菌和胡萝卜软腐欧文氏菌表现出增强的抗性。转基因植物表达天蚕素P1的能力传递给了后代。F1和F2植株具有正常表型(除了花色改变),并且自花授粉后保留了产生正常有活力种子的能力。选择了具有转基因性状孟德尔分离的F1植株品系。