首页> 外文OA文献 >Tissue-specific light-regulated expression directed by the promoter of a C4 gene, maize pyruvate,orthophosphate dikinase, in a C3 plant, rice.
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Tissue-specific light-regulated expression directed by the promoter of a C4 gene, maize pyruvate,orthophosphate dikinase, in a C3 plant, rice.

机译:在C3植物水稻中,由C4基因启动子玉米丙酮酸,正磷酸二激酶控制的组织特异性光调节表达。

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摘要

Pyruvate,orthophosphate dikinase (PPDK; EC 2.7.9.1) activity is abundant in leaves of C4 plants, while it is difficult to detect in leaves of C3 plants. Recent studies have indicated that C3 plants have a gene encoding PPDK, with a structure similar to that of PPDK in C4 plants. However, low expression makes PPDK detection difficult in C3 plants. This finding suggests that high PPDK expression in C4 plants is due to regulatory mechanisms which are not operative in C3 plants. We have introduced a chimeric gene consisting of the gene encoding beta-glucuronidase (GUS; EC 3.2.1.31) controlled by the PPDK promoter from a C4 plant, maize, into a C3 cereal, rice. The chimeric gene was exclusively expressed in photosynthetic organs, leaf blades and sheaths, and not in roots or stems. Histochemical analysis of GUS activity demonstrated high expression of the chimeric gene in photosynthetic organs, localized in mesophyll cells, and no or very low activity in other cells. GUS expression was also regulated by light in that it was low in etiolated leaves and was enhanced by illumination. These observations indicate that the mechanisms responsible for cell-specific and light-inducible regulation of PPDK observed in C4 plants are also present in C3 plants. We directly tested whether rice has DNA-binding protein(s) which interact with a previously identified cis-acting element of the C4-type gene. Gel retardation assays indicate the presence in rice of a protein which binds this element and is similar to a maize nuclear protein which binds PPDK in maize. Taken together, these results indicate that the regulatory system which controls PPDK expression in maize is not unique to C4 plants.
机译:丙酮酸,正磷酸二激酶(PPDK; EC 2.7.9.1)的活性在C4植物的叶子中很丰富,而在C3植物的叶子中很难检测到。最近的研究表明,C3植物具有一个编码PPDK的基因,其结构与C4植物中的PPDK相似。但是,低表达使C3植物中PPDK检测变得困难。该发现表明C4植物中高PPDK表达是由于在C3植物中不起作用的调节机制所致。我们已经从C4植物玉米中引入了一个由PPDK启动子控制的编码β-葡萄糖醛酸酶(GUS; EC 3.2.1.31)的基因组成的嵌合基因。嵌合基因仅在光合器官,叶片和鞘中表达,而不在根或茎中表达。对GUS活性的组织化学分析表明,嵌合基因在光合器官中高表达,位于叶肉细胞中,而在其他细胞中则没有或非常低。 GUS表达也受光调节,因为它在黄化叶片中较低,并且受光照增强。这些观察表明,在C3植物中也存在负责在C4植物中观察到的PPDK的细胞特异性和光诱导性调节的机制。我们直接测试了水稻是否具有与C4型基因先前鉴定的顺式作用元件相互作用的DNA结合蛋白。凝胶阻滞分析表明在水稻中存在一种结合该元素的蛋白质,类似于玉米中与PPDK结合的玉米核蛋白。综上所述,这些结果表明,控制玉米中PPDK表达的调控系统并非C4植物所独有。

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