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机构地区:[1]新疆大学生命科学与技术学院,新疆生物资源基因工程重点实验室,乌鲁木齐830046
出 处:《植物生理学通讯》2009年第5期449-454,共6页Plant Physiology Communications
基 金:新疆维吾尔自治区科技重大专项(200731138-3);教育部科学技术研究重点项目(205178)
摘 要:克隆获得包含完整开放阅读框(ORF)的灰绿藜液泡膜焦磷酸酶基因(CgVP1)cDNA序列,构建成基因表达载体pCAMBIA1301.1-CgVP1后,利用根癌农杆菌介导的花序浸染法转化拟南芥,再以抗性筛选方法获得了T3代纯合的转基因植株,经检测外源目的基因已经整合到拟南芥基因组中并能正常表达。分析结果表明,在拟南芥中过表达CgVP1基因后提高了植株抗盐胁迫的能力。The open reading frame (ORF) of halophyte Chenopodium glaucum tonoplast pyrophosphatase gene (CgVP1) was successfully cloned and inserted into plant expression vector pCAMBIA1301.1, then the recombinant (pCAMBIA 1301.1-Cg VP1) was transformed into A rabidopsis thaliana through floral dipping method, which was mediated by Agrobacterium tumefaciens. Homozygous T3 transgenic plants that were resistant to hygromycin were obtained. The results indicated that CgVP1 gene was integrated into Arabidopsis thaliana genome and expressed normally. Various salt tolerance analysis showed that that overexpression of tonoplast pyrophosphatase gene from Chenopodium glaucurn could improve the salttolerance in transgenic Arabidopsis thaliana.
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