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Negative regulation of phosphate starvation-induced genes

机译:磷酸饥饿诱导基因的负调控

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Phosphate (Pi) deficiency is a major nutritional problem faced by plants in many agro-ecosystems. This deficiency results in altered gene expression leading to physiological and morphological changes in plants. Altered gene expression is presumed to be due to interaction of regulatory sequences (cis-elements) present in the promoters with DNA binding factors (trans-factors). In this study, we analyzed the expression and DNA-protein interaction of promoter regions of Pi starvation-induced genes AtPT2 and TPSI1 AtPT2 encodes the high-affinity Pi transporter in Arabidopsis, whereas TPSI1 codes for a novel gene induced in the Pi-starved tomato (Lycopersicon esculentum). Expression of AtPT2 was induced rapidly under Pi deficiency and increased with decreasing concentrations of Pi. Abiotic stresses except Pi starvation had no affect on the expression of TPSI1 DNA mobility-shift assays indicated that specific sequences of AtPT2 and TPSI1 promoter interact with nuclear protein factors. Two regions of AtPT2 and TPSI1 promoters specifically bound nuclear protein factors from Pi-sufficient plants. Interestingly, the DNA binding activity disappeared during Pi starvation, leading to the hypothesis that Pi starvation-induced genes may be under negative regulation.
机译:磷酸盐(Pi)缺乏症是许多农业生态系统中植物面临的主要营养问题。这种缺陷导致基因表达的改变,导致植物的生理和形态变化。推测基因表达改变是由于存在于启动子中的调节序列(顺式元件)与DNA结合因子(反式因子)的相互作用。在这项研究中,我们分析了Pi饥饿诱导基因AtPT2和TPSI1的启动子区域的表达和DNA-蛋白质相互作用AtPT2编码拟南芥中的高亲和力Pi转运蛋白,而TPSI1编码在Pi饥饿番茄中诱导的新基因(Lycopersicon esculentum)。 Pi缺乏时迅速诱导AtPT2的表达,并随着Pi浓度的降低而增加。除Pi饥饿外的非生物胁迫对TPSI1的表达没有影响。DNA迁移分析表明AtPT2和TPSI1启动子的特定序列与核蛋白因子相互作用。 AtPT2和TPSI1启动子的两个区域特异性结合来自Pi充足植物的核蛋白因子。有趣的是,在Pi饥饿期间DNA结合活性消失了,导致了这样一个假设:Pi饥饿诱导的基因可能处于负调控之下。

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