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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >A 235-bp region from a nutritionally regulated soybean seed-specific gene promoter can confer its sulfur and nitrogen response to a constitutive promoter in aerial tissues of Arabidopsis thaliana
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A 235-bp region from a nutritionally regulated soybean seed-specific gene promoter can confer its sulfur and nitrogen response to a constitutive promoter in aerial tissues of Arabidopsis thaliana

机译:营养调控的大豆种子特异性基因启动子的235 bp区域可将其硫和氮响应赋予拟南芥气生组织中的组成型启动子

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摘要

The seed-specific promoter of the beta subunit gene of beta-conglycinin, a major seed storage protein of soybean, is upregulated in response to both sulfur and nitrogen nutrition. This response was studied in non-seed tissues of transgenic Arabidopsis thaliana by fusing the beta subunit promoter (Pbeta) downstream of an enhancer from the cauliflower mosaic virus 35S RNA promoter (P35S) and using the beta-glucuronidase (GUS) reporter gene. The chimeric promoter was upregulated by sulfur deficiency (AS), indicating that the Pbeta is able to direct the DeltaS response in non-seed tissues. Deletion analysis of the Pbeta revealed that, in seeds, the -307--73 bp region is sufficient for the DeltaS response. Insertion of the 235 bp region into the P35S conferred the DeltaS response on this constitutive promoter in both seed and non-seed tissues. The extent of upregulation by DeltaS was more evident when three of the 235 bp fragments were tandemly inserted into the P35S. The findings presented here suggest that a common mechanism exists for sulfur-regulated expression of the Pbeta in both seed and non-seed tissues and that this 235 bp region of the Pbeta is sufficient for regulation by both sulfur and nitrogen nutrition.
机译:β-伴大豆球蛋白的β亚基基因的种子特异性启动子是大豆的主要种子贮藏蛋白,其响应硫和氮营养而被上调。通过将花椰菜花叶病毒35S RNA启动子(P35S)的增强子下游的β亚基启动子(Pbeta)融合并使用β-葡糖醛酸糖苷酶(GUS)报告基因,在转基因拟南芥的非种子组织中研究了这种应答。嵌合启动子被硫缺乏(AS)上调,表明Pbeta能够指导非种子组织中的DeltaS反应。 Pbeta的缺失分析表明,在种子中,-307--73 bp区域足以满足DeltaS反应。在种子和非种子组织中,将235 bp区域插入P35S赋予该组成型启动子DeltaS反应。当将235 bp的三个片段串联插入P35S时,DeltaS的上调程度更加明显。此处提出的发现表明,在种子和非种子组织中均存在硫调节Pbeta表达的共同机制,并且Pbeta的235 bp区域足以通过硫和氮营养进行调节。

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