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作 者:吴燕川[1] 刘祥林[2] 印莉萍[2] 吴晓强 邱泽生 赵微平[2]
机构地区:[1]首都医科大学宣武医院多肽室 [2]首都师范大学生物系
出 处:《首都师范大学学报(自然科学版)》1998年第1期76-80,共5页Journal of Capital Normal University:Natural Science Edition
基 金:国家自然科学资金
摘 要:将满江红鱼腥藻glnA启动区与GUS报告基因连接,构成表达载体并导入烟草,在茎、叶中得到表达.这一结果为研究原核蓝藻与高等植物间转录因子识别、基因表达调控提供了有价值的信息,同时为构建实用载体开拓了新路. binary vector was constructed by inserting Anabaena azollae glnA promoter upstream of GUS reporter gene in an orientation. This expression vector was transformed into tobacco genomic DNA via Agrobacterium tumefaciens LBA4404mediated procedure. The transgenic tobaccos were obtained and the GUS activities in tobacco leaves and stems were examined histochemically. The result provided valuable information for the recognition of transcriptional factors the regulation of genes expression between prokaryotic cynobacteria and higher plant. This opens a new way for the construction of practical vectors.
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