首页 | 本学科首页   官方微博 | 高级检索  
     

农杆菌介导Ds转座因子的黄瓜遗传转化
引用本文:刘爱荣,陈双臣. 农杆菌介导Ds转座因子的黄瓜遗传转化[J]. 安徽农业科学, 2007, 35(23): 7047-7048
作者姓名:刘爱荣  陈双臣
作者单位:河南科技大学林学院,河南洛阳,471003;浙江大学农业与生物技术学院,浙江杭州,310029;河南科技大学林学院,河南洛阳,471003
基金项目:国家863项目:蔬菜分子标记育种技术和新品种选育(2003AA207120),河南科技大学人才基金资助
摘    要:以黄瓜品种"中农15"子叶外植体为试料,绿色荧光蛋白GFP基因为报告基因,利用农杆菌介导的遗传转化法将构建的激活表达标签pDsBar导入黄瓜,获得转基因黄瓜群体,对转化群体进行GFP基因活性及分子检测。结果表明,GFP已经整合到黄瓜基因组中;以Bar基因设计引物进行PCR检测表明,阳性率为72.3%;通过Southern杂交分析,发现26.0%为1个插入位点,51.0%为2个插入位点,T-DNA在基因组中的平均拷贝数为2.2个。

关 键 词:黄瓜  激活标签  绿色荧光蛋白基因  遗传转化
文章编号:0517-6611(2007)23-07047-02
修稿时间:2007-04-04

Agrobacterium-mediated Ds Transposon Transformation in Cucumber
LIU Ai-rong et al. Agrobacterium-mediated Ds Transposon Transformation in Cucumber[J]. Journal of Anhui Agricultural Sciences, 2007, 35(23): 7047-7048
Authors:LIU Ai-rong et al
Affiliation:College of Forestry, Henan University of Science and Techonology, Luoyang, Henan 471003
Abstract:The activation tagging pDsBar was transformed into cucumber via Agrobacterium-mediated with GFP as reporter genes.The transformed cucumber population was gained.GFP gene activation and molecular detection were conducted with the transformed plants.The results showed that GFP gene was interknitted into tomato genome.The positive rate was 72.3 % by PCR detection.Analyzed with southern blotting,about 26.0 % among T1 population with one inserted site and 51.0 % with two inserted sites were detected.The average inserted T-DNA sites was 2.2.
Keywords:Cucumber  Activation tagging  Green fluorescent protein  Transformation
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号