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A Brassica napus PHT1 phosphate transporter, BnPht1;4, promotes phosphate uptake and affects roots architecture of transgenic Arabidopsis

机译:甘蓝型油菜PHT1磷酸盐转运蛋白BnPht1; 4促进磷酸盐吸收并影响转基因拟南芥的根系结构

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Phosphorus (P) is one of the essential nutrient elements for plant development. In this work, BnPht1;4 gene, encoding a phosphate transporter of PHT1 family, was isolated from Brassica napus. BnPht1;4 possesses the major characteristic of PHT1 high-affinity Pi transporters in plants, such as plasma-membrane localization and 12 transmembrane-spanning domains. Quantitative reverse-transcription PCR analysis and promoter activity assay showed BnPht1;4 was inert in plants under Pi sufficient conditions. However, expression of this gene was remarkably enhanced in roots under Pi deficient conditions. Interestingly, under low Pi conditions, its promoter activity is impaired in tips of elongated roots, suggesting that the high-affinity Pi transporter may be not involved in low Pi response at root tip area. The experimental results also indicated that BnPht1;4 induction by Pi deficiency is dependent on the existence of sugar. In 35S:BnPht1;4 transgenic Arabidopsis, the increase of Pi availability resulted in the change of root architecture under Pi deficient conditions, showing longer primary roots and lower lateral root density than that of wild type. By cis-element analysis, two P1BS and two W-box elements were found in BnPht1;4 promoter. Yeast one-hybrid assay indicated that PHR1 could bind to the BnPht1;4 promoter. P1BS elements in BnPht1;4 promoter are essential for BnPht1;4 induction in Pi starvation response. Furthermore, WRKY75 could bind to the BnPht1;4 promoter, in which W-box elements are important for this binding. These results indicated BnPht1;4 may be dually controlled by two family regulators under low Pi responses. Thus, our data on the regulative mechanism of high-affinity Pi transporter in Pi starvation response will be valuable for B. napus molecular agriculture.
机译:磷(P)是植物发育必需的营养元素之一。在这项工作中,从甘蓝型油菜中分离出编码PHT1家族磷酸转运蛋白的BnPht1; 4基因。 BnPht1; 4具有植物中PHT1高亲和力Pi转运蛋白的主要特征,例如血浆膜定位和12个跨膜结构域。定量逆转录PCR分析和启动子活性测定表明,在Pi充足的条件下,BnPht1; 4在植物中是惰性的。然而,在缺乏Pi的条件下,该基因的表达在根中显着增强。有趣的是,在低Pi条件下,其延长根尖的启动子活性受到损害,这表明高亲和力Pi转运蛋白可能不参与根尖区域的低Pi响应。实验结果还表明,Pi缺乏引起的BnPht1; 4诱导依赖于糖的存在。在35S:BnPht1; 4转基因拟南芥中,Pi利用率的提高导致Pi缺乏条件下根系结构的变化,与野生型相比,Pi的根​​长更长,侧根密度更低。通过顺式元素分析,在BnPht1; 4启动子中发现了两个P1BS和两个W-box元素。酵母一杂交试验表明,PHR1可以结合BnPht1; 4启动子。 BnPht1; 4启动子中的P1BS元件对于Pi饥饿反应中的BnPht1; 4诱导至关重要。此外,WRKY75可以与BnPht1; 4启动子结合,其中W-box元件对于这种结合很重要。这些结果表明BnPht1; 4可能在低Pi响应下由两个家族调节剂双重控制。因此,我们关于高亲和力Pi转运蛋白在Pi饥饿反应中调控机制的数据对于油菜双歧杆菌分子农业将是有价值的。

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