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Cloning and characterization of the tomato karyopherin alpha 1 gene promoter.

机译:番茄核转运蛋白α1基因启动子的克隆与鉴定。

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摘要

The karyopherin alpha 1 (LeKAP alpha 1) gene of tomato (Lycopersicon esculentum) encodes a receptor involved in nuclear import. To analyze the expression pattern of this gene, a genomic clone containing its upstream region was isolated and sequenced. To study the promoter functionality, a 2170 bp fragment (LM1), was fused to glucuronidase (GUS) and introduced into petunia cells by particle bombardment. For further characterization of the promoter, one inverse and three deletion constructs were studied in cell suspension. To follow its expression in tobacco leaves, transgenic plants expressing GUS under the control of the LM1 promoter were made. Expression of LM1-GUS was largely restricted to actively growing leaf regions, suggesting possible involvement of active cell division and plant growth regulators in LeKAP alpha 1 expression.
机译:番茄(番茄(Lycopersicon esculentum))的karyopherin alpha 1(LeKAP alpha 1)基因编码参与核输入的受体。为了分析该基因的表达模式,分离了包含其上游区域的基因组克隆并进行了测序。为了研究启动子的功能,将2170 bp的片段(LM1)与葡萄糖醛酸酶(GUS)融合,并通过粒子轰击将其引入矮牵牛细胞中。为了进一步表征启动子,在细胞悬浮液中研究了一种反向和三种缺失构建体。为了追踪其在烟叶中的表达,制备了在LM1启动子控制下表达GUS的转基因植物。 LM1-GUS的表达在很大程度上限于活跃的叶片区域,这表明活跃的细胞分裂和植物生长调节剂可能参与了LeKAP alpha 1的表达。

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