Mukatira U T, Liu C, Varadarajan D K, Raghothama K G
Department of Horticulture and Landscape Architecture, Purdue University, West Lafayette, Indiana 47907-1165, USA.
Plant Physiol. 2001 Dec;127(4):1854-62.
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.
磷(Pi)缺乏是许多农业生态系统中植物面临的主要营养问题。这种缺乏会导致基因表达改变,进而引起植物生理和形态变化。基因表达改变被认为是由于启动子中存在的调控序列(顺式元件)与DNA结合因子(反式因子)相互作用所致。在本研究中,我们分析了磷饥饿诱导基因AtPT2和TPSI1启动子区域的表达及DNA-蛋白质相互作用。AtPT2编码拟南芥中的高亲和力磷转运蛋白,而TPSI1编码在缺磷番茄(番茄)中诱导的一个新基因。AtPT2的表达在磷缺乏时迅速诱导,并随着磷浓度降低而增加。除磷饥饿外的非生物胁迫对TPSI1的表达没有影响。DNA迁移率变动分析表明,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磷充足植物的核蛋白因子。有趣的是,在磷饥饿期间DNA结合活性消失,从而得出磷饥饿诱导基因可能受负调控的假说。