Ribot Cécile, Wang Yong, Poirier Yves
Department of Plant Molecular Biology, Biophore Building, University of Lausanne, Lausanne, Switzerland.
Planta. 2008 Apr;227(5):1025-36. doi: 10.1007/s00425-007-0677-x. Epub 2007 Dec 19.
The PHO1 protein is involved in loading inorganic phosphate (Pi) to the root xylem. Ten genes homologous to AtPHO1 are present in the Arabidopsis thaliana (L.) Heyn genome. From this gene family, transcript levels of only AtPHO1, AtPHO1;H1 and AtPHO1;H10 were increased by Pi-deficiency. While the up-regulation of AtPHO1;H1 and AtPHO1;H10 by Pi deficiency followed the same rapid kinetics and was dependent on the PHR1 transcription factor, phosphite only strongly suppressed the expression of AtPHO1;H1 and had a minor effect on AtPHO1;H10. Addition of sucrose was found to increase transcript levels of both AtPHO1 and AtPHO1;H1 in Pi-sufficient or Pi-deficient plants, but to suppress AtPHO1:H10 under the same conditions. Treatments of plants with auxin or cytokinin had contrasting effect depending on the gene and on the Pi status of the plants. Thus, while both hormones down-regulated expression of AtPHO1 independently of the plant Pi status, auxin and cytokinin up-regulated AtPHO1;H1 and AtPHO1;H10 expression in Pi-sufficient plants and down-regulated expression in Pi-deficient plants. Treatments with abscisic acid inhibited AtPHO1 and AtPHO1;H1 expression in both Pi-sufficient and Pi-deficient plants, but increased AtPHO1;H10 expression under the same conditions. The inhibition of expression by abscisic acid of AtPHO1 and AtPHO1;H1, and of the Pi-starvation responsive genes AtPHT1;1 and AtIPS1, was dependant on the ABI1 type 2C protein phosphatase. These results reveal that various levels of cross talk between the signal transduction pathways to Pi, sucrose and phytohormones are involved in the regulation of expression of the three AtPHO1 homologues.
PHO1蛋白参与将无机磷酸盐(Pi)装载到根木质部。拟南芥(L.)海恩基因组中存在10个与AtPHO1同源的基因。在这个基因家族中,只有AtPHO1、AtPHO1;H1和AtPHO1;H10的转录水平会因Pi缺乏而升高。虽然Pi缺乏对AtPHO1;H1和AtPHO1;H10的上调遵循相同的快速动力学,且依赖于PHR1转录因子,但亚磷酸盐仅强烈抑制AtPHO1;H1的表达,对AtPHO1;H10的影响较小。研究发现,添加蔗糖会增加Pi充足或Pi缺乏植物中AtPHO1和AtPHO1;H1的转录水平,但在相同条件下会抑制AtPHO1:H10。用生长素或细胞分裂素处理植物会产生不同的效果,这取决于基因和植物的Pi状态。因此,虽然这两种激素均独立于植物的Pi状态下调AtPHO1的表达,但生长素和细胞分裂素在Pi充足的植物中上调AtPHO1;H1和AtPHO1;H10的表达,而在Pi缺乏的植物中下调表达。用脱落酸处理会抑制Pi充足和Pi缺乏植物中AtPHO1和AtPHO1;H1的表达,但在相同条件下会增加AtPHO1;Hio的表达。脱落酸对AtPHO1和AtPHO1;H1以及Pi饥饿反应基因AtPHT1;1和AtIPS1表达的抑制作用依赖于ABI1型2C蛋白磷酸酶。这些结果表明,Pi、蔗糖和植物激素信号转导途径之间存在不同程度的相互作用,参与了三种AtPHO1同源物表达的调控。