Plastids rely on multiple phosphate (Pi) transport activities to support and control a wide range of metabolic processes, including photosynthesis and carbon partitioning. Five of the six members of the PHT4 family of Pi transporters in Arabidopsis thaliana (PHT4;1-PHT4;5) are confirmed or predicted plastid proteins. As a step towards identifying the roles of individual PHT4 Pi transporters in chloroplast and non-photosynthetic plastid Pi dynamics, we used promoter-reporter gene fusions and quantitative RT-PCR studies, respectively, to determine spatial and diurnal gene expression patterns. PHT4;1 and PHT4;4 were both expressed predominantly in photosynthetic tissues, although expression of PHT4;1 was circadian and PHT4;4 was induced by light. PHT4;3 and PHT4;5 were expressed mainly in leaf phloem. PHT4;2 was expressed throughout the root, and exhibited a diurnal pattern with peak transcript levels in the dark. The remaining member of this gene family, PHT4;6, encodes a Golgi-localized protein and was expressed ubiquitously. The overlapping but distinct expression patterns for these genes suggest specialized roles for the encoded transporters in multiple types of differentiated plastids. Phylogenetic analysis revealed conservation of each of the orthologous members of the PHT4 family in Arabidopsis and rice, which is consistent with specialization, and suggests that the individual members of this transporter family diverged prior to the divergence of monocots and dicots.
IntroductionDynamic control of stromal inorganic phosphate (Pi) levels is central to the specialized metabolic functions of differentiated plastids. Notably, the concentration of Pi in the chloroplast stroma is tightly coordinated with environmental conditions to modulate both photosynthesis and the subsequent partitioning of fixed carbon. 1,2 Pi concentrations in amyloplasts also are held within a critical limit to prevent inhibition of starch biosynthesis. 3 For each plastid type, Pi concentrations are controlled through a combination of metabolic recycling in the stroma and surrounding cytosol, and the transport of Pi across the plastid limiting membrane. Recent data suggest that similar processes also link the Pi status of the chloroplast stroma and thylakoid lumen. 4 Plastidic Pi transport is generally attributed to members of the plastidic phosphate translocator (pPT) family. 5 These proteins are located in the inner envelope membrane and mediate strict counterexchange of Pi for phosphorylated C3, C5 or C6 compounds. The triose phosphate/Pi translocator (TPT) was the first pPT protein to be identified, and it is expressed almost exclusively in photosynthetic tissues where it catalyzes transport of cytosolic Pi into the chloroplast in exchange for triose phosphates, the end products of photosynthesis. 6 This activity represents the major pathway for carbon allocation to the cytosol during the day as well as the primary route for Pi import into the chloroplast. Related members of the pPT family include the phosphoenolpyruvate/Pi translocator...