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来自热带树木细叶木麻黄的一种类金属硫蛋白基因的启动子在一年生双子叶植物和单子叶植物中均具有活性。

The promoter of a metallothionein-like gene from the tropical tree Casuarina glauca is active in both annual dicotyledonous and monocotyledonous plants.

作者信息

Ahmadi Nour, Dellerme Sabine, Laplaze Laurent, Guermache Fathia, Auguy Florence, Duhoux Emile, Bogusz Didier, Guiderdoni Emmanuel, Franche Claudine

机构信息

Calim and Biotrop Programmes, CIRAD, Avenue Agropolis, 34398 Montpellier Cedex 5, France.

出版信息

Transgenic Res. 2003 Jun;12(3):271-81. doi: 10.1023/a:1023365003210.

DOI:10.1023/a:1023365003210
PMID:12779116
Abstract

A chimeric gene consisting of the beta-glucuronidase (gusA) reporter gene under the control of the metallothionein-like promoter cgMT1 from the tropical tree Casuarina glauca was introduced into Nicotiana tabacum via Agrobacterium tumefaciens and into Oryza sativa by particle bombardment. The strongest histochemical staining for GUS activity was observed in the root system of the transgenic plants, and especially in lateral roots. In contrast, a relatively low level of reporter gene expression was seen in the aerial tissues and GUS staining was located mainly in the plant vascular system. The average ratio of GUS activity between root and leaf was found to be 13:1 in tobacco and 1.5:1 in rice. The pattern of cgMT1 promoter activity in floral organs was found to be different in tobacco and rice. High levels of gusA gene expression were detected in the ovules, pollen grains and tapetum, whereas in rice PcgMT1 directs expression to the vascular system of the floral organs. These results suggest that PcgMT1 is potentially useful in molecular breeding to express genes of interest whose products are preferentially needed in roots.

摘要

一个嵌合基因由热带树木桤木的类金属硫蛋白启动子cgMT1控制下的β-葡萄糖醛酸酶(gusA)报告基因组成,通过根癌农杆菌导入烟草,并通过粒子轰击导入水稻。在转基因植物的根系中观察到最强的GUS活性组织化学染色,特别是在侧根中。相比之下,地上组织中报告基因的表达水平相对较低,GUS染色主要位于植物维管系统中。烟草中根与叶的GUS活性平均比值为13:1,水稻中为1.5:1。发现cgMT1启动子在花器官中的活性模式在烟草和水稻中有所不同。在胚珠、花粉粒和绒毡层中检测到高水平的gusA基因表达,而在水稻中PcgMT1将表达导向花器官的维管系统。这些结果表明,PcgMT1在分子育种中可能有用,可用于表达其产物优先在根中需要的感兴趣基因。

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Duplication of CaMV 35S Promoter Sequences Creates a Strong Enhancer for Plant Genes.CaMV 35S 启动子序列的重复产生了植物基因的强启动子。
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