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Cloning and functional characterization of the promoter of PsSEOF1 gene from Pisum sativum under different stress conditions using Agrobacterium-mediated transient assay

机译:农杆菌介导的瞬时分析法在不同胁迫条件下来自豌豆的PsSEOF1基因启动子的克隆及功能鉴定

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摘要

PsSEOF1, a SEO (sieve element occlusion) gene family protein (forisome) is calcium powered motor protein and is located close to plasma membrane of sieve element. In sieve element (SE) it senses the calcium ion levels and undergoes ATP-independent conformational shifts. Forisome, meaning gate-bodies (Latin foris: wing of a gate; Greek soma: body). Recent reports show that SEO gene family protein can prevent the loss of nutrient rich photoassimilate upon wound injury. The regulation of SEO protein forisome under abiotic/ biotic stress is still unknown. The analysis of cis-regulatory element present in the upstream region is not well understood. Tissue specific promoters guarantee correct expression when it perceives particular stimuli. Here we report isolation of tissue specific promoter of PsSEOF1 was isolated by gene walking PCR from P. sativum (pea) genomic DNA library constructed by BD genome walker kit. In silico analysis revealed several putative cis element within this promoter sequence like wound response, cold, dehydration. Putative elements which might be required for its vascular tissue specificity has also been identified. The GUS activities of PsSEOF1 promoter-GUS chimeric construct in the agroinfiltrated leaves under different environmental stress abiotic and biotic like wound, cold, salt and phytohormones has shown high level of GUS activity. To identify the activity of PsSEOF1 promoter under different stress condition an Agrobacterium-mediated transient expression of tobacco plants were subjected to histochemical GUS staining. Stress-inducible nature of PsSEOF1 promoter opens possibility for the study of the PsSEOF1 gene regulation under stress condition. The isolated promoter sequence could serve as an important candidate for tissue specific promoter in genetic engineering of plant under stress conditions.
机译:PsSEOF1是SEO(筛子元素闭塞)基因家族蛋白(胞体),是钙驱动的运动蛋白,位于筛子元素的质膜附近。在筛分元件(SE)中,它感应钙离子水平并经历不依赖ATP的构象转变。太棒了,意为门身(拉丁语foris:门的翅膀;希腊语soma:身体)。最近的报道表明,SEO基因家族蛋白可以防止创伤后富含营养的光同化物的损失。在非生物/生物胁迫下对SEO蛋白主要酶的调节仍是未知的。对上游区域存在的顺式调节元件的分析尚不十分清楚。组织特异性启动子在感知到特定刺激时保证正确表达。在这里,我们报告通过基因步行PCR从由BD基因组步行者试剂盒构建的豌豆(豌豆)基因组DNA文库中通过基因步行PCR分离了PsSEOF1的组织特异性启动子。在计算机分析中,在该启动子序列中发现了几种推定的顺式元件,如伤口反应,冷,脱水。还已经确定了其血管组织特异性可能需要的推定元件。在不同环境胁迫下,非生物和生物体(如伤口,感冒,盐和植物激素),农杆菌浸润叶片中PsSEOF1启动子-GUS嵌合构建体的GUS活性显示出高水平的GUS活性。为了鉴定在不同胁迫条件下PsSEOF1启动子的活性,对农杆菌介导的烟草植物的瞬时表达进行了组织化学GUS染色。 PsSEOF1启动子的应激诱导性质为研究应激条件下PsSEOF1基因调控提供了可能。分离的启动子序列可以作为植物在胁迫条件下的基因工程中组织特异性启动子的重要候选者。

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