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Vol. 18, Issue 11, 4438-4445, November 2007
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Institute of Plant Sciences, Eidgenössiche Technische Hochschule Zurich, 8092 Zurich, Switzerland
Submitted May 16, 2007;
Revised August 20, 2007;
Accepted August 28, 2007
Monitoring Editor: Suresh Subramani
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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) and furthermore, many pathways are known to be involved in poly P metabolism (Freimoser et al., 2006), it is still not known how this polymer is synthesized in yeast or any higher eukaryote. To learn more about the regulation of the metabolism of phosphate and poly P, we performed a detailed study of the yeast phosphate transporters, the PHO pathway, and poly P levels.
The yeast genome encodes five phosphate transporters (Pho84, Pho87, Pho89, Pho90, and Pho91) that are involved in the intricately regulated phosphate uptake (Wykoff and O'Shea, 2001). Pho84 and Pho89 are two high-affinity transporters that are both regulated by the PHO pathway (Bun-Ya et al., 1991; Martinez and Persson, 1998): Under low-phosphate conditions, the transcription factor Pho4 is dephosphorylated and localized in the nucleus, where it activates transcription of phosphate-regulated genes such as PHO84 and PHO89 (Lenburg and O'Shea, 1996; O'Neill et al., 1996; Springer et al., 2003). In the high-phosphate state, Pho4 is phosphorylated by the cyclin-dependent kinase Pho85, which causes its relocalization to the cytosol and concomitant down-regulation of phosphate responsive genes (Lenburg and O'Shea, 1996; O'Neill et al., 1996; Springer et al., 2003). Despite its strict regulation by the PHO pathway, Pho84 is the most important phosphate transporter in yeast, even in high-phosphate media (Wykoff and O'Shea, 2001). Transcription of PHO84 and PHO89 is not only regulated by the PHO pathway, but for example, also by the SAGA and the SWI-SNF complexes (Lee et al., 2000; Sudarsanam et al., 2000; Bhaumik and Green, 2002) or by shifts to acidic or alkaline pH, the calcineurine pathway, or the cell cycle (Causton et al., 2001; Serrano et al., 2002; Ruiz et al., 2003; Luan and Li, 2004). In the absence of the high-affinity transporters, the low-affinity transporters, Pho87, Pho90, and Pho91, are necessary for phosphate transport, but otherwise exhibit few phenotypes if deleted (Wykoff and O'Shea, 2001). In addition to phosphate uptake, the three low-affinity phosphate transporters are involved in the external sensing of phosphate and the regulation of the phosphate-signaling pathway (Auesukaree et al., 2003; Giots et al., 2003; Pinson et al., 2004).
The PHO pathway has been characterized in great detail by studying secreted acid phosphatase (rAPase) activity, PHO84 transcription, and Pho84 localization, or trehalase activity (Petersson et al., 1999; Auesukaree et al., 2003, 2004; Giots et al., 2003; Pinson et al., 2004; Huang and O'Shea, 2005) and because of its function as a phosphate store, poly P was specifically studied as a potential regulator (Neef and Kladde, 2003; Auesukaree et al., 2004; Thomas and O'Shea, 2005). But the regulation of poly P metabolism by the PHO pathway and by phosphate transporters has not been studied systematically. Here, we used the poly P content as the read-out for a thorough characterization of mutant strains affected in the five phosphate transporters. With poly P content as a distinguishing mark, it was possible to define novel functions of the low-affinity phosphate transporters in phosphate, poly P, and general cell metabolism. Most notably, we suggest that Pho91 is an intracellular phosphate transporter that exports phosphate from the vacuole and thereby regulates intracellular phosphate homeostasis and poly P levels.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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), which were generated in the background of the strain BY4741 (MATa his3
1 leu20 met150 ura30; Brachmann et al., 1998). A detailed listing of all strains used and created in this study is given in Table 1.
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; Werner et al., 2005). The strains EY57 and EY916-EY922 were a gift from Dr. E. O'Shea (Harvard University) and Dr. D. Wykoff (Villanova University) and were maintained on YPGal medium (YPD medium containing 20 g/l galactose instead of glucose; Wykoff and O'Shea, 2001). Strains harboring plasmids were kept on SC medium lacking the corresponding amino acid (0.68 g/l yeast nitrogen base, complete supplement dropout mix [both either from Qbiogene, Carlsbad, CA, or Formedium, Norfolk, United Kingdom], 20 g/l glucose). For poly P analysis, strains were always precultured for 3 d, and fresh medium was inoculated to an OD600 = 1. Cells were harvested at different time points, dissolved in 1 M H2SO4, and stored at –20°C until extraction.
Manipulation of Yeast Strains
Plasmids were transformed into yeast by the method of Gietz et al. (1992). The kanamycin marker in the YKO strains was replaced with either the nourseothricine (natMX4, clonNat) or the hygromycin (hphMX4) resistance gene by transformation with Not I-digested plasmids pAG25 (natMX4) or pAG32 (hphMX4; Goldstein and McCusker, 1999), respectively. To inactivate two genes, these markers were amplified with flanking up- and downstream genomic sequences (with the "A" and "D" primers). Double deletion strains were created by transforming existing single YKO strains with these PCR products following the high-efficiency yeast transformation protocol (Gietz and Woods, 2002). Some double deletions were also created by crossing a bait strain to selected single YKO strains (Tong et al., 2001) or by crossing and tetrad dissection according to standard procedures (Kaiser et al., 1994). All strains showed almost identical phenotypes irrespective of the method used for their generation. All double deletion strains were verified by PCR with the "A," "B," and kanB primers. The yeast phosphate transporters Pho87, Pho90, and Pho91 were endogenously tagged with green fluorescent protein (GFP) at the N-terminus by the PCR-based epitope-tagging strategy (Janke et al., 2004). The sequences encoding the GFP and/or the different promoters were amplified with the S1 and S4 primer pair from the plasmids pYM-N9, pYM-N13, pYM-N17, pYM-N18, and pYM-N21 (for the ADH, CYC1, GPD, and TEF promoters, respectively; Janke et al., 2004). In the resulting strains the endogenous promoter is replaced with a ADH, CYC1, GPD, or TEF promoter, and the GFP tag is fused to the N-terminus of the Pho87, Pho90, or Pho91. The correct fusion of the N-terminal GFP with Pho91 was also verified by sequencing the region of the junction of these two parts. Pho84 was tagged by integrating a PCR fragment of the GFP tag and a HIS-selection marker (amplified with the S2 and S3 primers from the plasmid pYM28) at the C-terminus.
DNA Manipulations
Yeast genomic DNA was isolated following the smash-and-grab protocol (Rose et al., 1990). Modified versions of the plasmids pRS416-ADH, pRS416-TEF, and pRS426-GPD (Mumberg et al., 1995) were made by the introduction of the sequence for one hemagglutinin (HA) tag. The novel plasmids (pRS416-ADH-HA, pRS416-TEF-HA, and pRS426-GPD-HA) allow C-terminal HA tag fusions by cloning using the XmaI restriction site. The gene encoding PHO84 was cloned into the above mentioned vectors with the restriction sites EcoRI and XmaI that were included in the primers used for amplification. The insert in the resulting construct (pRS416-ADH-HA-PHO84, pRS416-TEF-HA-PHO84, and pRS426-GPD-HA-PHO84) were verified by sequencing.
Quantification of Poly P and Total Phosphate Content
Poly P was extracted, purified, and quantified as previously described (Werner et al., 2005). In short, 1 OD600 equivalent of cells was harvested and pelleted. The supernatant was removed, 50 µl 1 M H2SO4 was added, and the suspension was neutralized with 50 µl 2 M NaOH and 100 µl Tris-malate buffer (1 M Tris, 0.5 M malate, pH 7.5, 6% neutral red solution [0.1% neutral red in 70% ethanol]). Cell fragments were removed by centrifugation. After addition of 600 µl 6 M NaI, the extracts were applied to Qiagen PCR purification columns (Chatsworth, CA). The columns were washed twice with wash buffer (10 mM Tris buffer, pH 7.5, 50% ethanol, 1 mM EDTA, and 100 mM NaCl). Poly P was eluted in 100 µl H2O, and 50 µl of this eluate was specifically digested with Saccharomyces cerevisiae exopolyphosphatase. To quantify the released phosphate, 86 µl of 28 mM ammonium heptamolybdate (in 2.1 M H2SO4) and 64 µl of 1.6 mM malachite green (in 0.35% polyvinyl alcohol) were added. The malachite green solution was measured in a BioTek PowerWaveTM XS microplate spectrophotometer (BioTek Instruments, Winooski, VT) at 600 nm and compared with that of phosphate standards (5–100 µM Pi; Cogan et al., 1999). To quantify total phosphate content, 0.5 OD600 equivalent of cells were pelleted, resuspended in 200 µl 1 M H2SO4, and heated in a boiling water bath for 20 min. Released phosphate was quantified as described above.
Acid Phosphatase Assay
Acid Phosphatase (rAPase) activity was assayed according to Huang and O'Shea (2005) in 50 µl cell suspension by adding 200 µl p-nitrophenyl-phosphate (20 mM in 100 mM sodium acetate, pH 4.2). After 5–15 min reaction time at 28°C, 200 µl of 10% ice-cold trichloroacetic acid and 400 µl sodium carbonate solution (2 M) were added, and the OD420 was measured. The measurements were normalized with the cell density (OD600), the reaction time, and the sample volume (in ml). rAPase activity (Miller units) was obtained by multiplying the normalized OD420 values with a factor of 1000.
-Galactosidase Reporter Assay
The PHO84-lacZ and the ACT1-lacZ reporter plasmids have been described earlier (Hughes et al., 2001) and were a gift from Dr. S. Fields (University of Washington). The -galactosidase reporter assay was performed similar to the protocols of Möckli and Auerbach (2004) and Miller (1972). To 10 µl of a yeast culture, 500 µl Z-buffer (60 mM Na2HPO4, 40 mM NaH2PO4, 10 mM KCl, 1 mM MgSO4, 50 mM -mercaptoethanol, pH 7), 10 µl CHCl3, and 15 µl SDS (0.2%) were added. The cells were briefly vortexed and incubated for 5 min at 28°C, and the reaction was started by the addition of 100 µl ONPG solution (4 mg/ml O-nitrophenyl -D-galactopyranoside in Z-buffer). As soon as the solution turned yellow, the reaction was stopped by the addition of 250 µl of 2 M Na2CO3 solution. The cells were spun down, and absorption in the supernatant was measured at 420 nm. The values were normalized with the reaction time, the cell density (OD600), and the sample volume (in ml). LacZ activity (Miller units) was calculated by multiplication with 1000. For each strain three independent transformants were measured, and all experiments were performed at least twice.
FM4-64 Staining and Confocal Microscopy
Vacuoles were stained with FM4-64 as described (Vida and Emr, 1995). In short, yeast cultures were grown in YPD or YPD-Pi to an OD600 
0.5–2, and 3 OD600 units were concentrated in 100 µl YPD (or YPD-Pi) and stained at 30°C for 15–20 min with 60 µM FM4-64 (8 mM stock solution in DMSO). Cells were pelleted (700 x g, 3 min), resuspended in 5 ml YPD (or YPD-Pi), and shaken at 30°C for 45–60 min, and then the cells were washed three times with 1 ml PBS (4 mM KH2PO4, 16 mM Na2HPO4, 8.7 mM NaCl, pH 7.3) or TBS (50 mM Tris, 150 mM NaCl, pH 7.5, for cells grown in YPD-Pi). Cells were then applied to agarose-coated microscope slides (Hailey et al., 2002) and observed with a confocal laser scanning microscope (Leica DM IRBE and Leica TCS SP laser; Leica, Unterentfelden, Switzerland) using an ArKr laser at 488 and 568 nm for excitation. Pictures of the stained samples and their controls were not processed digitally except for overlay of different channels and contrast adjustments.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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strain even showed a slight but not significant increase in poly P (Figure 1). To further characterize the effect of each phosphate transporter on poly P levels in yeast, the mutant strains expressing only one of the five transporters (Wykoff and O'Shea, 2001) were tested. The strain that contains Pho84 but lacks all other phosphate transporters (EY918) had poly P levels similar to the wild-type strain (EY57; Figure 2). However, none of the other phosphate transporters could support measurable amounts of poly P by itself (Figure 2). This suggested that Pho84 is the most important transporter for the maintenance of normal poly P levels.
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Strain). It is also known that the deletion of PHO85 results in the constitutive up-regulation of the PHO pathway and that PHO84 is one of the most strongly up-regulated genes (Ogawa et al., 2000). Therefore, we tested if the poly P hyperaccumulation phenotype of the pho85 strains correlated with up-regulation of PHO84. Poly P content in the double deletion strain of PHO84 and PHO85 was strongly reduced and lower than in the strain lacking only PHO84 (Figure 3). We therefore conclude that up-regulation of Pho84 is essential for poly P hyperaccumulation in the pho85 strain. In addition to PHO84, we also tested the influence of the other four phosphate transporters in a pho85 strain background. Because these transporters, except Pho87, contribute only minimally to phosphate uptake and showed a weaker poly P phenotype, it was expected that these four double deletion strains would have the same poly P phenotype as the strain with an inactivated PHO85 gene. Unexpectedly, the deletion of the different phosphate transporters in the strain lacking PHO85 had a much stronger effect on poly P levels than that observed in the single deletions of the five transporters (Figure 3). The poly P levels in the double deletions strains of PHO85 and PHO89 were little affected, but the deletion of PHO87, PHO90, or PHO91 in the pho85 strain background caused an increase of poly P levels (Figure 3). The pho85 pho87 strain usually showed slightly increased poly P levels by a factor of 1.5–2, while the double deletion of PHO85 with either PHO90 or PHO91 caused 3 - 4 times higher poly P content as compared with the pho85 strain (Figure 3). Contrary to the poly P levels, total phosphate content in these strains changed less. Consequently, the pho85 pho87, pho85 pho90, and the pho85 pho91 strains stored more of their total phosphate as poly P (Figure 3). From these results we conclude that the low-affinity phosphate transporters suppress poly P levels in cells with a constitutively up-regulated PHO pathway, i.e., in PHO85 mutant cells.
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background all three low-affinity phosphate transporters (Pho87, Pho90, and Pho91) limited poly P levels (Figure 1). Therefore, we further characterized their effect on the metabolism of phosphate and poly P. The inhibitory effect of Pho87, Pho90, and Pho91 on poly P levels in the pho85 strain could have been caused by a repression of the PHO pathway and Pho84 levels or localization. As a measure for the activation of the PHO pathway, we determined rAPase activity in the single and double deletion strains that were used for the poly P measurements. In comparison to wild type, and as shown previously (Huang and O'Shea, 2005), rAPase activity was strongly increased in the pho85 strain, but only insignificantly higher in the pho87 and pho91 strains (Figure 4A). The double deletion strains of PHO90 or PHO91 with PHO85 secreted very similar rAPase levels as the pho85 strain and only the pho85 pho87 double deletion strain exhibited minimally reduced rAPase activity (Figure 4A). Neither did the double deletion of PHO85 and PHO87, PHO90 or PHO91 significantly alter transcription from the PHO84 promoter as shown by -galactosidase activities in a LacZ-reporter assay (determined with the actin [ACT1] promoter as a reference; Figure 4B). However, the pho87 and pho90 and to a lesser extent also the pho91 single deletion strains showed strongly up-regulated transcription from the PHO84 promoter, even though these strains did not accumulate more poly P. This suggests that the low-affinity phosphate transporters influence PHO84 transcription by still unknown mechanism. Because Pho84 is regulated posttranslationally by internalization and degradation in the vacuole, it was tested if Pho91 represses the effect of PHO84 overexpression or affects Pho84 localization at the plasma membrane. The overexpression of PHO84 in a pho91 strain did not cause a stronger poly P increase (compared with the strain with the empty plasmid) than in the wild type (Figure 4C). Overexpression of PHO84 in the other two single deletion strains or in the pho84 strain restored wild-type poly P levels (Figure 4C). Finally, Pho84 localization at the plasma membrane was not abolished by the deletion of PHO87, PHO90, or PHO91. Pho84-GFP could be detected at the plasma membrane, inside the vacuole and presumably within the endoplasmic reticulum in cells grown in low-phosphate and in normal YPD medium, albeit the latter resulted in a much weaker signal in all compartments. However, Pho84 was slightly less frequently and less strongly internalized in the vacuole in the strains lacking PHO90 or PHO91 compared with the wild-type and the pho87 strain (Figure 5). On the other hand, the deletion of PHO87 had no apparent effect on the localization of Pho84-GFP under the conditions tested. Based on the rAPase measurements, the reporter gene assays and Pho84 localization, it was concluded that the low-affinity phosphate transporters Pho87, Pho90, and Pho91 only lightly affect the PHO pathway, PHO84 expression, and PHO84 function. This small effect on the PHO pathway seemed unlikely to account for the large poly P increase that was observed in the pho85 strain upon the deletion of PHO90 or PHO91.
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. In agreement with the assumed function as a part of a low-affinity phosphate uptake and/or sensing system, Pho87 and Pho90 localized to the plasma membrane independent of the promoter that was used (Figure 6). In contrast, Pho91 showed a distinct localization in intracellular membranes, which colocalized with FM4-64 staining (Figure 6). This colocalization of the FM4-64 signal with the staining from the GFP-Pho91 fusion protein placed the Pho91 transporter in the vacuolar membrane. GFP-Pho91 was always detected in the vacuole, irrespective of the promoter used and even when expressed from the weak CYC1 promoter (Figure 6). Furthermore, the vacuolar localization of Pho91 was independent of Pho86 (Figure 6), Pho87 or Pho90 (not shown). We therefore concluded that Pho91 is a vacuolar phosphate transporter and that the vacuolar localization was not an artifact of overexpression. In addition to the signal from the vacuolar periphery, we also observed bright fluorescence from clusters in or at the vacuolar membrane, mostly between adjacent vacuoles (Figure 6). These clusters became more abundant as the yeast cultures approached stationary phase and were less frequently found in cells grown in SC medium compared with YPD. Brightly stained clusters were also more abundant in a pho85 background (Figure 6). However, despite the numerous clusters at interfaces between adjacent vacuoles or vesicles in the pho85 strain, the GFP-Pho91 signal was still detected from the entire vacuolar periphery. These clusters could also have been an artifact from overexpression because they were less frequent if GFP-Pho91 was expressed from the weak CYC1 promoter. To test if the N-terminally GFP-tagged Pho91 protein was still functional, poly P was quantified in the wild-type and pho85 strains with and without the GFP tag (Figure 7). The poly P content in the PHO85 deletion strain containing the GFP-tagged Pho91 transporter increased only slightly, which indicated a functional fusion protein (Figure 7). To the contrary, the promoter exchange alone and introduction of the GFP-Pho91 fusion protein in the wild type rather reduced poly P levels (Figure 7), supposedly due to the presumptive overexpression of PHO91. This effect was much more apparent in the wild-type background (Figure 7). From these localization results it was thus concluded that active Pho91 is localized in the vacuolar membrane.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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; Freimoser et al., 2006). Because of the obvious importance of phosphate uptake for the synthesis of poly P, we chose the phosphate transporters and the PHO pathway as a starting point to disentangle this complex regulation of the poly P metabolism in yeast. To test if the five yeast phosphate transporters differentially affect poly P metabolism, we compared poly P levels in the single deletion strains of the five transporters and in strains that contain only one of all five transporters. In all media tested, the inactivation of PHO84 caused the lowest poly P total, roughly half that of the wild-type strain, and only Pho84 (and none of the other transporters) conferred a normal poly P state if present as the only phosphate transporter. Thus, Pho84 is the most important phosphate transporter for poly P metabolism; irrespective of the growth medium, growth stage, or pH of the medium (not shown).
Next, we analyzed the poly P state after deletion of either one of the five phosphate transporters in the background of a pho85 strain. It had previously been shown that constitutive up-regulation of the PHO pathway, by the deletion of PHO85, causes strongly increased poly P levels (McDonald et al., 2001). This increase was completely abolished by the additional deletion of PHO84, which suggested that up-regulation of PHO84 was required for poly P hyperaccumulation in the pho85 strain. However, deletion of many other genes that are also involved in poly P metabolism, for example, the VTC genes, also abolishes or diminishes poly P hyperaccumulation in the pho85 strain (data not shown). Surprisingly, the pho84 pho85 double deletion strain contained less poly P than the pho84 single deletion strain. This suggests that some of the (numerous) effects of a PHO85 deletion reduce poly P levels but that this phenotype is masked by the drastically increased phosphate uptake due to the up-regulation of PHO84. If Pho84 is indeed the determining transporter for poly P metabolism, the removal of any one of the other transporters (PHO87, PHO89, PHO90, or PHO91) in the pho85 strain should not suppress the poly P hyperaccumulation caused by the deletion of PHO85. Unexpectedly, combination of the PHO87, PHO90, or PHO91 inactivation with the PHO85 deletion strongly increased poly P hyperaccumulation compared with the pho85 strain. Although deletion of PHO90 and PHO91 did not have a significant effect on poly P content in the single deletion strains, it caused strong and highly significant poly P hyperaccumulation in the pho85 background. Interestingly, the double deletion strains also showed an altered phosphate allocation: The total phosphate content increased much less than the poly P content and consequently the proportion of phosphate fixed as poly P was 
2–4 times higher than in the single deletion strains. Next, we attempted to further characterize the involvement of all three low-affinity transporters in phosphate and poly P metabolism.
The double deletion strains (pho85 pho87, pho85 pho90, and pho85 pho91) had neither a strongly altered rAPase activity nor did they up-regulate PHO84. In addition, Pho84 localization at the plasma membrane, and internalization in the vacuole was not affected by PHO87 and only slightly dependent on PHO90 or PHO91. The pho90 and pho91 strains showed slightly less internalized Pho84 than in the wild type or in the strain lacking PHO87. This suggests that the increased poly P hyperaccumulation was not caused by a general up-regulation of the PHO pathway. In contrast, Pho90 and Pho91 affected the relative poly P content and must therefore be involved in intracellular phosphate allocation. However, a triple deletion of PHO85, PHO90, and PHO91 did not result in a further increased poly P content compared with the pho85 pho90 and the pho85 pho91 double deletion strains (not shown). Consequently, Pho90 and Pho91 do not perform redundant functions and must exert their effect on poly P metabolism by different mechanisms. We therefore conclude that Pho90 and Pho91 act independently in the regulation of phosphate metabolism or in intracellular phosphate transport.
Within the context of the global analysis of all yeast proteins Huh et al. (2003) localized Pho90 and Pho91 to the ER, and Pho87 could not be localized definitively. Therefore, there is little experimental evidence to support the widely held view that Pho87, Pho90, and Pho91 function in phosphate uptake from the environment across the plasma membrane (Wykoff and O'Shea, 2001; Auesukaree et al., 2003; Giots et al., 2003; Pinson et al., 2004). Because our poly P data could be explained by an intracellular localization and functioning of either Pho87, Pho90, or Pho91, localization of these low-affinity phosphate transporters was specifically addressed.
Although Pho87 and Pho90 were indeed clearly localized to the plasma membrane, the GFP-Pho91 fusion protein revealed a clear and unmistakable localization in the vacuolar membrane. It is therefore suggested that Pho91 serves as a vacuolar phosphate transporter that exports Pi from the vacuolar lumen to the cytosol. According to this model, a deletion of PHO91 blocks phosphate export from the vacuole, which could in turn impair degradation of the vacuolar poly P pool. A pho85 pho91 strain would thus not take up more phosphate compared with the pho85 single deletion strain, but more phosphate would be "trapped" in the form of poly P because of the reduced poly P degradation and phosphate export. This hypothesis also implies that the vacuolar poly P pool does not exert a strong negative feedback regulation on poly P synthesis in strains lacking PHO91. In contrast to Pho91, the observation that Pho90 limits poly P accumulation cannot be explained by its action as a phosphate transporter per se, because it was clearly localized in the plasma membrane, where it would be involved in phosphate uptake. At present, it is hypothesized that Pho90 must have a regulatory or sensory function that is involved in controlling phosphate allocation. Indeed, Pho87 or Pho90 and Pho91 have been suggested to serve as components of an external phosphate sensor (Giots et al., 2003; Pinson et al., 2004). However, more detailed studies will be necessary to identify the exact function of Pho87 and Pho90 in poly P metabolism.
In summary, we have shown that among the five described yeast phosphate transporters, Pho84 is the most important protein for poly P metabolism. In the absence of Pho84, poly P levels were reduced by at least 50%. Surprisingly, the low-affinity transporters Pho87, Pho90, and Pho91 negatively regulate poly P levels, which was most apparent in a pho85 background with a constitutively up-regulated PHO pathway. We could not detect a direct regulatory influence of Pho91 on the PHO pathway or on Pho84. Instead, it was found that Pho91 localizes to the vacuolar membrane. We therefore suggest that Pho91 is an intracellular phosphate transporter that affects poly P levels by regulating intracellular phosphate allocation and organellar phosphate levels.
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ACKNOWLEGMENTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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Footnotes |
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Address correspondence to: Florian M. Freimoser (ffreimoser{at}ethz.ch)
Abbreviations used: GFP, green fluorescent protein; HA, hemagglutinin; poly P, inorganic polyphosphate; rAPase, acid phosphatase; SC medium, synthetic complete medium; YPD, yeast peptone dextrose.
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REFERENCES |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEGMENTSREFERENCES |
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, left y-axis) and total phosphate (P tot, 
, right y-axis) levels in single deletion strains of the five yeast phosphate transporters. The six strains were grown in YPD medium, and samples were taken at different time points. The figure shows only the measurements of the samples harvested after 4 h (late exponential phase). The bars represent the mean of four poly P extractions and quantifications, and the SD is indicated.
