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Activation of a Bean Chitinase Promoter in Transgenic Tobacco Plants by Phytopathogenic Fungi.

机译:植物致病真菌在转基因烟草植物中激活豆几丁质酶启动子。

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摘要

The temporal and spatial expression of a bean chitinase promoter has been investigated in response to fungal attack. Analysis of transgenic tobacco plants containing a chimeric gene composed of a 1.7-kilobase fragment carrying the chitinase 5B gene promoter fused to the coding region of the gus A gene indicated that the chitinase promoter is activated during attack by the fungal pathogens Botrytis cinerea, Rhizoctonia solani, and Sclerotium rolfsii. Although induction of [beta]-glucuronidase activity was observed in tissues that had not been exposed to these phytopathogens, the greatest induction occurred in and around the site of fungal infection. The increase in [beta]-glucuronidase activity closely paralleled the increase in endogenous tobacco chitinase activity produced in response to fungal infection. Thus, the chitinase 5B-gus A fusion gene may be used to analyze the cellular and molecular details of the activation of the host defense system during pathogen attack.
机译:已经研究了响应于真菌侵袭的豆几丁质酶启动子的时空表达。对含有由融合了gus A基因编码区的几丁质酶5B基因启动子的1.7碱基碱基片段组成的嵌合基因的转基因烟草植物的分析表明,几丁质酶启动子在真菌病原体灰葡萄孢(Botrytis cinerea,Rhizoctonia solani)的攻击过程中被激活。和Sclerotium rolfsii。尽管在未暴露于这些植物病原体的组织中观察到了β-葡萄糖醛酸苷酶活性的诱导,但是最大的诱导发生在真菌感染部位及其周围。 β-葡糖醛酸糖苷酶活性的增加与响应真菌感染而产生的内源烟草几丁质酶活性的增加非常相似。因此,几丁质酶5B-gus A融合基因可用于分析病原体侵袭期间宿主防御系统激活的细胞和分子细节。

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