Zhang Hui, Zhao Lingxia, Chen Yuhui, Cui Lijie, Ren Weiwei, Tang Kexuan
Plant Biotechnology Research Center, School of Agriculture and Biology, Fudan-Shanghai Jiaotong University (SJTU)-Nottingham Plant Biotechnology R&D Center, SJTU, Shanghai 200030, People's Republic of China.
Biotechnol Appl Biochem. 2007 Oct;48(Pt 2):101-7. doi: 10.1042/ba20060224.
In the present study, a plant binary expression vector PG-pRD12-hFIX (where PG is polygalacturonase) harbouring the hFIX (human coagulation Factor IX) gene was constructed and introduced into tomato (Lycopersicon esculentum) via Agrobacterium tumefaciens-mediated transformation. After kanamycin selection, 32 putative independent transgenic tomato plants were regenerated. PCR and Southern-blot analyses confirmed the transgenic status of some plants. RT (reverse transcription)-PCR analysis for the expression of the introduced gene (hFIX) demonstrated that the hFIX gene was expressed specifically in fruits of the tomato. Western-blot analysis confirmed the presence of a 56 kDa band specific to hFIX in the transformed tomatoes. ELISA results showed that the expression of hFIX protein reached a maximum of 15.84 ng/g fresh weight in mature fruit. A blood-clotting assay demonstrated the clotting activity of the expressed hFIX protein in transgenic tomato fruits. This is the first report on the expression of hFIX in plants, and our research provides potentially valuable knowledge for further development of the plant-derived therapeutic proteins.
在本研究中,构建了一个携带人凝血因子IX(hFIX)基因的植物双元表达载体PG-pRD12-hFIX(其中PG是多聚半乳糖醛酸酶),并通过根癌农杆菌介导的转化方法将其导入番茄(Lycopersicon esculentum)。经过卡那霉素筛选,再生出32株假定的独立转基因番茄植株。PCR和Southern杂交分析证实了部分植株的转基因状态。对导入基因(hFIX)表达的逆转录PCR(RT-PCR)分析表明,hFIX基因在番茄果实中特异性表达。Western杂交分析证实了在转化的番茄中存在一条56 kDa的hFIX特异性条带。酶联免疫吸附测定(ELISA)结果显示,hFIX蛋白在成熟果实中的表达量最高达到15.84 ng/g鲜重。凝血试验证明了转基因番茄果实中表达的hFIX蛋白具有凝血活性。这是关于hFIX在植物中表达的首次报道,我们的研究为植物源治疗性蛋白的进一步开发提供了潜在的宝贵知识。