Rothstein S J, Lahners K N, Lotstein R J, Carozzi N B, Jayne S M, Rice D A
Gene. 1987;53(2-3):153-61. doi: 10.1016/0378-1119(87)90003-5.
We have constructed a set of plant transformation vectors, promoter cassettes, and chimeric antibiotic-resistance genes for the transformation and expression of foreign genes in plants sensitive to Agrobacterium infection. The different vectors allow for either concurrent or consecutive selection for kanamycin and hygromycin resistance and have a number of unique restriction sites for the insertion of additional DNA. The promoter cassettes utilize the CaMV 19S and CaMV 35S promoters and are constructed to allow for the easy insertion of foreign genes. The cloned gene can then easily be inserted into the transformation vectors. We have utilized the promoter cassettes to express the hygromycin-resistance gene either from the CaMV 35S or the CaMV 19S promoters, with both chimeric resistance genes allowing for the selection of hygromycin-resistant tobacco plants.
我们构建了一组植物转化载体、启动子盒和嵌合抗生素抗性基因,用于在对农杆菌感染敏感的植物中转化和表达外源基因。不同的载体允许对卡那霉素和潮霉素抗性进行同时或连续选择,并且具有多个独特的限制性酶切位点,用于插入额外的DNA。启动子盒利用花椰菜花叶病毒(CaMV)19S和CaMV 35S启动子构建,便于外源基因的插入。然后,克隆的基因可以很容易地插入到转化载体中。我们利用启动子盒从CaMV 35S或CaMV 19S启动子表达潮霉素抗性基因,两种嵌合抗性基因都能用于筛选抗潮霉素的烟草植株。