• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of plntcellLink to Publisher's site
Plant Cell. Sep 2011; 23(9): 3482–3497.
Published online Sep 27, 2011. doi:  10.1105/tpc.111.089581
PMCID: PMC3203450

The Arabidopsis Na+/H+ Antiporters NHX1 and NHX2 Control Vacuolar pH and K+ Homeostasis to Regulate Growth, Flower Development, and Reproduction[C][W]

Abstract

Intracellular Na+/H+ (NHX) antiporters have important roles in cellular pH and Na+, K+ homeostasis. The six Arabidopsis thaliana intracellular NHX members are divided into two groups, endosomal (NHX5 and NHX6) and vacuolar (NHX1 to NHX4). Of the vacuolar members, NHX1 has been characterized functionally, but the remaining members have largely unknown roles. Using reverse genetics, we show that, unlike the single knockouts nhx1 or nhx2, the double knockout nhx1 nhx2 had significantly reduced growth, smaller cells, shorter hypocotyls in etiolated seedlings and abnormal stamens in mature flowers. Filaments of nhx1 nhx2 did not elongate and lacked the ability to dehisce and release pollen, resulting in a near lack of silique formation. Pollen viability and germination was not affected. Quantification of vacuolar pH and intravacuolar K+ concentrations indicated that nhx1 nhx2 vacuoles were more acidic and accumulated only 30% of the wild-type K+ concentration, highlighting the roles of NHX1 and NHX2 in mediating vacuolar K+/H+ exchange. Growth under added Na+, but not K+, partly rescued the flower and growth phenotypes. Our results demonstrate the roles of NHX1 and NHX2 in regulating intravacuolar K+ and pH, which are essential to cell expansion and flower development.

INTRODUCTION

Ion homeostasis and the regulation of cellular pH are associated with every aspect of the biology of the cell. The concerted action of H+-translocating enzymes (H+-pumps) and cation/H+ exchangers are vital to establish and maintain optimal ion and pH gradients, which are essential for cell function and plant development (Martinoia et al., 2007; Amtmann and Leigh, 2010). Intracellular Na+/H+ antiporters (NHXs) are integral membrane proteins residing in the plasma membrane (Shi et al., 2000) endosomal compartments (Rodriguez-Rosales et al., 2008; Bassil et al., 2011), and vacuoles (Apse et al., 1999; Yokoi et al., 2002; Apse and Blumwald, 2007; Hamaji et al., 2009; Leidi et al., 2010). They belong to the monovalent cation/proton antiporter (CPA1) family of transporters (Maser et al., 2001). In plants, NHX antiporters catalyze the electroneutral exchange of Na+ and/or K+ for H+ by using the electrochemical H+ gradients generated by the (H+)–ATPases (in the plasma membrane) and the (H+)–ATPase and (H+)–PPase (in the vacuole) to direct either the movement of Na+ or K+ out of the cell or the luminal movement of Na+ or K+ into the vacuoles and intracellular organelles. The NHX gene family of Arabidopsis thaliana includes a class of six intracellular NHX-type antiporters, which are classified into two groups (Brett et al., 2005a; Pardo et al., 2006; Rodriguez-Rosales et al., 2009). Group I contains NHX1 to NHX4 and localizes to vacuoles, whereas group II contains NHX5 and NHX6 and localizes to endosomal compartments (Bassil et al., 2011). Several functions have been associated with plant NHX transporters, including the regulation of flower coloration (Yamaguchi et al., 2001; Ohnishi et al., 2005; Yoshida et al., 2009), the regulation of cellular K+ homeostasis (Venema et al., 2003; Pardo et al., 2006; Apse and Blumwald, 2007; Leidi et al., 2010), cell expansion (Apse et al., 2003; Bassil et al., 2011), vesicular trafficking and protein targeting (Bowers et al., 2000; Brett et al., 2005b; Bassil et al., 2011), and salt tolerance (Apse et al., 1999; Hernandez et al., 2009; Bassil et al., 2011). NHX1 was shown to be required for seedling establishment and leaf development, especially in the formation of large epidermal cells (Apse et al., 2003). Recently, NHX5 and NHX6 were shown to be localized in the Golgi and trans-Golgi network and to function in the trafficking of endosomal cargo to the vacuole, in salt stress, and in cell expansion (Bassil et al., 2011). However, the roles of the remaining members of the vacuolar group, NHX2, NHX3, and NHX4, in growth and development remain largely unknown. To comprehend the concerted role of all intracellular NHXs, an effort to generate and characterize multiple knockout lines of Arabidopsis NHX1 to NHX6 was initiated.

Although we have considerable information about the molecular and biochemical networks acting during plant growth and development, we have little knowledge of how cells regulate the transport of solutes and their intracellular pH. Ions (K+ in particular) and pH gradients have a great effect on the regulation of cell volume and the trafficking of membrane vesicles and their protein cargo between the different cellular compartments (Blumwald, 1987; Pardo et al., 2006; Bassil et al., 2011). These processes are essential for plant growth, development, and the response to environmental changes.

NHX-type cation/H+ antiporters are critical players in cell expansion. To understand the concerted role of intracellular Arabidopsis NHXs on cell expansion, we initiated the characterization of the growth and development of NHX1 and NHX2 knockout lines. We show that NHX1 and NHX2 function together to control cell expansion in vegetative tissues and male reproductive organs and are required for normal flower development and set. We link flower developmental processes to altered vacuolar pH and K+ homeostasis and argue that NHX1 and NHX2 mediate K+/H+ exchange to accumulate K+ in the vacuole, a critical step for cell expansion and growth, especially in rapidly expanding cells.

RESULTS

At the organ level, the expression of NHX1 and NHX2 indicated that both genes are expressed ubiquitously, including roots, rosette leaves, stems, flowers, and siliques (see Supplemental Figure 1 online). The level of expression of NHX1 was significantly higher than that of NHX2 in all organs examined, and NHX2 expression levels were similar to that of other NHX members (Bassil et al., 2011). The nearly ubiquitous expression of NHX1 was also confirmed in publicly available expression data (http://bbc.botany.utoronto.ca/efp/cgi-bin/efpWeb.cgi) as wells as previously published work (Yokoi et al., 2002; Aharon et al., 2003; Apse et al., 2003).

NHX1 and NHX2 Colocalize to the Vacuole

To assess the localization of NHX1 and NHX2 and their possible vacuolar colocalization, we generated plants expressing C-terminal translational fusion reporter constructs with NHX1 fused with green fluorescent protein (GFP), or NHX2 fused with yellow fluorescent protein (YFP) or red fluorescent protein (RFP), driven by either the Ubiquitin-10 (Ub10) or 35S promoters. The growth of the transgenic reporter lines was indistinguishable from that of the wild-type plants, indicating that the fusion proteins did not adversely affect the growth of the transgenic plants. In 35S-NHX2-YFP plants, the fluorescence signals in roots and root tips localized to vacuolar membranes (Figure 1; see Supplemental Figure 2 online). The vacuolar localization was clearly indicated by the nuclei seen outside the fluorescent boundary delineated by the NHX2-associated YFP signal (arrows in Figure 1A). Transvacuolar cytoplasmic strands were also clearly evident in root cells, which further supported the NHX2-YFP vacuolar association. Observation of 35S-NHX1-GFP reporter plants resulted in a poor and inconsistent GFP signal that was often observed within the vacuolar lumen and endosomal bodies in all lines examined (see Supplemental Figure 2 online). To circumvent possible problems associated with overexpression or nonstable expression caused by the 35S promoter, NHX1-GFP was expressed under the control of the Ub10 promoter, which enabled a milder, more stable expression of downstream genes (Grefen et al., 2010). Transient transformation of Ub10-NHX1-GFP in Arabidopsis seedlings resulted in a GFP signal associated with vacuolar membranes and transvacuolar strands (Figure 1B; see Supplemental Movie 1 online). Furthermore, plasmolysis of root cells, induced by the addition of 1 M mannitol, caused a clear recession of the tonoplast and the YFP and GFP signals, supporting the vacuolar localization of NHX1 and NHX2 (see Supplemental Figure 2 online). To determine whether NHX1 and NHX2 colocalize, Ub10-NHX1-GFP and 35S-NHX2-RFP were transiently coexpressed in Arabidopsis seedlings. As shown in Figures 1C to to1E,1E, NHX1-GFP and NHX2-RFP were highly colocalized to vacuolar membranes in cells expressing both transgenes. We also tested whether NHX1 colocalized with another vacuolar membrane protein by transiently expressing Ub10-NHX1-GFP in stable reporter lines of VAMP711-RFP, a R-SNARE of the tonoplast (Uemura et al., 2004). As expected, NHX1-GFP colocalized extensively with VAMP711 (Figures 1F to to1H1H).

Figure 1.
Subcellular Localization of NHX1 and NHX2.

nhx1 nhx2 Double Knockout Phenotypes

To investigate NHX1 and NHX2 functions, we used a reverse genetic approach to generate knockouts from available T-DNA insertion lines. Two independent knockout mutants using different T-DNA insertion lines for each gene were identified. Single knockouts, designated as nhx1-1, nhx1-2, nhx2-1, and nhx2-3 (see Methods), were genotyped and backcrossed twice before their subsequent use in crosses to generate the independent double knockout lines nhx1-1 nhx2-1, nhx1-2 nhx2-1, and nhx1-2 nhx2-3 (see Supplemental Figure 3 online). Lack of expression of full-length NHX1 and NHX2 in all knockouts was confirmed with RT-PCR (see Supplemental Figure 3 online). Experiments using the double knockout lines produced identical results; therefore, unless otherwise noted, results reported from here on are those obtained with the line nhx1-1 nhx2-1.

The single knockout nhx1 displayed reduced growth compared with the wild type (Columbia ecotype [Col-0]), similar to that reported previously in nhx1 in the Wassilewskija ecotype background (Apse et al., 2003). However, nhx2 did not show any obvious growth phenotypes or developmental defects when grown either in soil (Figure 2A) or on plates (see below). By contrast, the double knockout nhx1 nhx2 displayed a significant reduction in growth (Figure 2). Rosette leaf size and inflorescence height were markedly smaller than either the wild type or the single knockouts. Cross sections through leaf margins indicated that nhx1 nhx2 cells were significantly smaller than comparable wild-type leaf cells (Figure 2B). nhx1 nhx2 leaf tissue remained highly organized with no apparent cell-type disruptions. To confirm the nhx1 nhx2 phenotypes, we complemented nhx1 nhx2 with functional copies of both genes. Transformation of nhx1 nhx2 with either 35S-NHX1-GFP or 35S-NHX2-YFP reverted the growth phenotype to the wild type (Figure 2C), thereby demonstrating that the nhx1 nhx2 phenotypes were caused by disruption of NHX1 and NHX2. In addition, C-terminal tagging of NHX1 and NHX2 did not affect the function of either protein.

Figure 2.
Growth and Development of the Single and Double Knockouts of NHX1 and NHX2.

Stamens of nhx1 nhx2 Lack Filament Elongation and Anther Dehiscence

nhx1 nhx2 plants displayed significant phenotypes in their reproductive organs. nhx1 nhx2 flowers developed a low number of siliques, which contained few or no seeds (Figure 2D; see arrows). At the same developmental stage, nhx1 nhx2 flowers were significantly shorter and narrower than the wild-type flowers (Figures 3A to to3C).3C). A closer examination of flower anatomy revealed at least two distinct developmental changes associated with stamens. First, mature nhx1 nhx2 stamens had markedly shorter filaments that did not extend far enough to position the anthers at the height of the stigma (Figures 3B [arrows] and and3D),3D), as is typically seen in the wild-type flowers. Quantitative measurements of filament lengths indicated that, in nhx1 nhx2 flowers, both short and long filaments were reduced in length (Figure 3D). A comparison of longitudinal sections of filaments revealed that nhx1 nhx2 filament cells were only 55% the length and 60% the width of the wild-type filament cells (Figures 3E to to3G).3G). The second stamen phenotype was that nhx1 nhx2 anthers did not dehisce at the same frequency seen in the wild-type anthers (Figures 3B and and3C3C [insets]). Scoring of anthers from 40 nhx1 nhx2 plants (~80 anthers) indicated that only 3% showed normal anther dehiscence. Cross sections of anthers showed that, in a high proportion of nhx1 nhx2 anthers, the stomium (St in Figures 3H and and3I)3I) did not rupture sufficiently to release pollen from individual anther locules (Figures 3H and and3I).3I). When anther dehiscence did occur it was not sufficient to release and expose the majority of pollen. Therefore, nhx1 nhx2 anthers lacked the characteristic yellowish color typical of anthers after dehiscence and remained the distinctive color of immature anthers (i.e., off-white) (Figures 3A and and3B3B [insets]). Eventually nhx1 nhx2 flowers senesced without setting, and inflorescences of nhx1 nhx2 did not form siliques (Figure 2B). A comparison of flower anatomy, the lack of anther dehiscence, and filament elongation in nhx1 nhx2 are shown in the scanning electron micrographs of Figure 4.

Figure 3.
Stamens of the Double Knockout nhx1 nhx2 Have Reduced Filament Elongation and Anther Dehiscence.
Figure 4.
Scanning Electron Micrographs Comparing the Anatomy of the Wild-Type and nhx1 nhx2 Flowers.

To test specific expression of NHX1 and NHX2 in floral organs, we used NHX1 and NHX2 promoters to drive β-glucuronidase (GUS) expression in transgenic plants (see Supplemental Figure 4 online). GUS analysis indicated that the expression of NHX1 was abundant in most flower organs (see Supplemental Figure 4A online) but was low in nonelongated filaments and immature anthers (see Supplemental Figure 4B online) and was highly expressed in elongated filaments (see Supplemental Figure 4C online). On the other hand, NHX2 was highly expressed in anthers and pollen. These results might suggest developmental-specific expression patterns for NHX1 and NHX2 and explain the flower phenotype that was observed in nhx1 nhx2 but not in either nhx1 or nhx2 single knockouts. In addition, promoter GUS analysis indicated that NHX1 was expressed throughout seedlings in all organs, whereas NHX2 was expressed, albeit to a lesser extent, in root and shoot meristems and seedling vasculature (see Supplemental Figure 4 online).

Pollen Viability and Germination Were Not Affected in nhx1 nhx2 Plants

The expression of NHX1 and NHX2 seen in pollen (see Supplemental Figure 4 online) prompted us to investigate whether pollen germination and viability were affected in nhx1 nhx2 plants. For viability and germination experiments, approximately twice the number of nhx1 nhx2 flowers were needed to obtain similar amounts of pollen as were obtained from the wild type, probably because of the poor anther dehiscence in nhx1 nhx2. Pollen viability was examined by hydrating pollen on solidified gelatin and staining with 4′,6-diamidino-2-phenylindole (DAPI) (Alandete-Saez et al., 2008). No differences were detected in the rate or extent of pollen hydration between the wild type and nhx1 nhx2 (Figure 5) or in pollen development, because DAPI staining of grains revealed that nhx1 nhx2 had three nuclei (i.e., pollen mitosis I and II occurred normally) (Figures 5B and and5D).5D). Pollen germination in nhx1 nhx2 did not differ significantly from the wild type (Figure 5E). To determine which gametophyte was responsible for the nhx1 nhx2 phenotype, reciprocal crosses were performed between the wild type and nhx1 nhx2. When the wild type was used as the female and nhx1 nhx2 was used as a pollen donor (Wt/KO in Figures 5F and and5G),5G), no effect on flower set was seen, and only a minor but nonsignificant reduction in silique length was observed compared with the wild-type control. These results suggest that nhx1 nhx2 pollen tubes grew normally in vivo. However, when the wild type was used as the pollen donor to pollinate nhx1 nhx2 emasculated plants (i.e., KO/Wt), only 74% of the flowers set, and the silique length was significantly shorter compared with Wt/KO or Wt/Wt controls. When nhx1 nhx2 was self-pollinated (KO/KO), only 49% of flowers set, and silique length was only marginally lower compared with KO/Wt crosses (Figures 5F and and5G).5G). These results suggest that the lack of flower set and silique formation in nhx1 nhx2 might not be due to lack of pollen viability or germination. In addition to the stamen abnormalities discussed above, the impaired growth of the nhx1 nhx2 female gametophyte should be considered.

Figure 5.
Pollen Viability and Germination Is Not Significantly Affected in the nhx1 nhx2 Double Knockout.

The Presence of NaCl in the Growth Medium Reduced nhx1 nhx2 Flower and Growth Phenotypes

To gain additional insight into the role of NHX1 and NHX2 in vegetative and reproductive growth, nhx1 nhx2 plants were grown under different salinity conditions. A clear difference was observed between nhx1 nhx2 plants grown in the presence and absence of 100 mM NaCl (Figures 6A and and6B).6B). Unlike nhx1 nhx2 grown in the absence of salt, nhx1 nhx2 plants grown on 100 mM NaCl were able to produce siliques (Figures 6A and and6B).6B). A closer examination of the flowers revealed that in salt-grown nhx1 nhx2 plants, the filaments were fully elongated, and the anthers dehisced (Figures 6C to to6E).6E). A quantification of flower set indicated that nhx1 nhx2 flower set increased from 8% in nonsaline conditions to 57% on 100 mM NaCl (Figure 6F). These results would suggest that Na+ ions partially substituted the lack of K+ accumulation in filament cell vacuoles.

Figure 6.
The nhx1 nhx2 Flower Phenotype Is Rescued When Plants Are Grown in High Salt.

Given the roles of NHX-type transporters in Na+ and K+ homeostasis (Pardo et al., 2006; Apse and Blumwald, 2007), we assessed whether the growth of nhx1 nhx2 was affected by varying the concentrations of K+ and Na+ in the growth media. The growth of the wild-type plants in media supplemented with either 30 mM of Na+ or K+ or equimolar concentrations of both did not differ significantly (Figure 7). The biomass of nhx1 nhx2, however, increased at 30 mM Na+ compared with nhx1 nhx2 grown in control media (i.e., 1 mM Na+ and 1 mM K+) but remained significantly lower than the biomass of the wild-type plants grown at 30 mM Na+. Moreover, in the presence of 30 mM K+, the growth of nhx1 nhx2 decreased by 30% compared with that of nhx1 nhx2 plants grown in control media, and was only 5% the weight of the wild-type plants (Figure 7I). A close-up of nhx1 nhx2 plants in the 30 mM K+ treatment indicated that the rosette formed a tight ball composed of curled leaves that lacked leaf and petiole expansion compared with nhx1 nhx2 in the high Na+ or control treatments (Figure 7J). Plants also displayed severe yellowing and necrosis of some leaves. In addition, in the presence of 30 mM K+, nhx1 nhx2 roots were profusely curled, forming concentric circles and a partial loss of growth toward the axis of gravity (Figure 7K). Under an equimolar concentration of Na+ plus K+ (30 mM each), the weight of nhx1 nhx2 plants increased only moderately, and although it was higher than that of seedlings grown in control media, it remained significantly lower than that of the wild type (Figure 7I). The negative effects of K+ on growth of nhx1 nhx2 plants were also observed in experiments that used KNO3 instead of KCl as a salt source. Identical results were also obtained when dry weights were used for the same analysis. These results indicate that moderate amounts of Na+ in the media improved growth of nhx1 nhx2, whereas an equimolar amount of K+ was unfavorable to growth.

Figure 7.
Growth and Ion Content of the nhx1 nhx2 Double Knockout Depends on K+ and Na+ in Media.

In wild-type plants, leaf K+ and Na+ contents increased with increased K+ and Na+ in the media (see Supplemental Figure 5 online). The leaf concentrations of K+ were higher than those of Na+ in all treatments and genotypes tested. Furthermore, the wild-type leaf K+ content was higher than that of nhx1 nhx2 leaves from all treatments. Leaf K+ contents were also influenced by the presence of Na+ in the media and differed substantially between the wild type and nhx1 nhx2. For example, in the wild type, there was a small but significant increase in leaf K+ content in plants grown in 30 mM Na+ compared with plants grown in control media. In 30 mM Na+–grown nhx1 nhx2 plants, leaf K+ content was lower than of control-grown plants. In nhx1 nhx2, leaf Na+ contents did not differ in media with added K+. The differential leaf K+ content was also reflected by the K+:Na+ ratio, which was halved in nhx1 nhx2 plants grown in all treatments (Figure 7J). The Na+:K+ ratio was also significantly higher in nhx1 nhx2 than in the wild type at both 30 mM Na+ and 30 mM Na+ plus 30 mM K+ treatments. Collectively, these data indicate that the ability of nhx1 nhx2 plants to accumulate K+ in favor of Na+ was compromised and that these plants were not able to adjust their K+ content when challenged with Na+, as seen in the wild-type plants.

Etiolation of nhx1 nhx2 Seedlings Is Cation Dependent

We reasoned that a good experimental system to test the role(s) of NHX1 and NHX2 in rapid cell expansion would be the etiolation response of dark-grown seedlings, because etiolated seedlings are amenable to physiological and cellular measurements of pH and K+ homeostasis. Furthermore, the rapid elongation of hypocotyls in etiolated seedlings closely parallels the elongation of anther filaments during flower development. When grown on solidified media in the dark, nhx1 nhx2 etiolated seedlings displayed significantly shorter hypocotyls and longer roots than the wild-type seedlings (see Supplemental Figure 6A online). Etiolated seedlings grown on increasing concentrations of K+ exhibited a progressively stronger phenotype (i.e., significantly shorter hypocotyls and longer roots than control-grown nhx1 nhx2). Interestingly, when K+ concentrations in the media were 10 mM or more, roots of nhx1 nhx2 grew by curling away from the direction of gravity, forming concentric circles of winding roots, which was probably caused by uneven expansion of epidermal cells (see Supplemental Figure 6 online). Similar to the response of long-term plant growth experiments (Figure 7), hypocotyls of nhx1 nhx2 seedlings grown in 30 mM Na+ elongated more than those of nhx1 nhx2 in control media and were not significantly different in length from the wild-type hypocotyls. The root response, however, did not recover under increased Na+ as it did in hypocotyls. The consistent phenotype and response of etiolated seedlings allowed for a reliable experimental system to perform additional cellular measurements (as described below).

NHX1 and NHX2 Regulate Vacuolar pH and K+ Homeostasis

To assess the roles of NHX1 and NHX2 in pH regulation, we used the ratiometric fluorescein-based pH sensitive dye, 2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF) in an imaging-based approach to measure vacuolar pH in vivo. Ratiometric dyes have the distinct advantage of not being significantly affected by dye loading, cell size, or tissue morphology, unlike other nonratiometric dyes. The membrane-permeant BCECF-acetoxymethyl (AM) derivative readily loads into vacuoles of intact root cells (Swanson et al., 1998; Krebs et al., 2010). pH values were calculated from fluorescence ratios of confocal images using an in situ calibration curve (see Supplemental Figure 7 online). Because of the imaging nature of the technique, it was possible to measure vacuolar pH along the entire root zone of seedlings from root tip to hypocotyl. Vacuolar pH in root tip cells (i.e., cells that were not fully expanded, as seen in Supplemental Figure 7B online), was lower (pH 5.5) than in the mature zone (pH 6.3 to 5.8) but was similar to that in hypocotyl cells (pH 5.5 to 5.2) (Figure 8A). In root tip cells, no significant difference between the wild-type and nhx1 nhx2 vacuolar pH was observed. However, in cells of the mature root zone and the hypocotyl, vacuolar pH was nearly 0.5 and 0.35 pH units lower, respectively, in nhx1 nhx2 (Figure 8A). Figures 8B and and8C8C show the typical ratio images showing the BCECF-associated vacuolar fluorescence in mature root zone cells from the wild type and nhx1 nhx2.

Figure 8.
Vacuoles of nhx1 nhx2 in Root and Hypocotyl Cells Are More Acidic and Contain Less K+ than Comparable Wild-Type Cells.

We next measured vacuolar K+ with a similar imaging approach (to that of pH discussed above), using the ratiometric K+-sensitive dye potassium-binding benzofuran isophthalate acetoxymethyl ester (PBFI-AM) (Halperin and Lynch, 2003). We found that a longer incubation time was needed to load the AM form of the dye into the vacuole of cortical and hypocotyl cells than was reported for loading into the cytosol of root hair cells (Halperin and Lynch, 2003). The vacuolar localization of the dye was confirmed using confocal images of root tip cells, in which it is easy to discern vacuole from cytosol (see Supplemental Figure 7B online). Under our experimental conditions, the vacuolar K+ concentrations of root cells of the mature zone as well as hypocotyl cells were ~75 mM (±12 mM). In nhx1 nhx2, however, K+ concentrations were significantly lower and were near 20 mM (±4 mM). Both a lower vacuolar pH and lower K+ concentration in nhx1 nhx2 are consistent with the notion of tonoplast-localized NHX1 and NHX2 mediating vacuolar K+/H+ exchange.

DISCUSSION

The in planta localization of NHX1 and NHX2 provides key information on their functions. In Arabidopsis cell cultures, Hamaji et al. (2009) immunolocalized NHX1 to vacuoles, and Yokoi et al. (2002) transiently expressed NHX2 in onion epidermal cells to show vacuolar localization, whereas Apse et al. (1999) used membrane fractionation to localize NHX1 to the tonoplast. Here we show that NHX1 and NHX2 colocalize to the vacuole. We also observed that in some reporter lines, the NHX1-GFP signal was associated with punctate and motile endosomal bodies in addition to labeling of the vacuole. Although this might be an artifact of the 35S promoter-driver expression, it is interesting to note that Hamaji et al. (2009) also observed similarly sized vesicles that were immunolabeled with NHX1 in salt-treated plants. They suggested that NHX1 may have roles in salt stress, either through tonoplast augmentation via vesicular trafficking, or that NHX1 in an endosomal or prevacuolar compartment may be critical for salt stress, as suggested by Hernandez et al. (2009). A role of NHX1 in vesicular trafficking was also inferred from microarray analysis of nhx1 transcripts, in which many vesicular trafficking genes were differentially expressed (Sottosanto et al., 2004).

Using a reverse genetic approach, we characterized the growth and development phenotypes of several T-DNA insertion lines of NHX1 and NHX2. In the Col-0 background, nhx1 knockout plants displayed a similar reduction in growth as described previously for nhx1 in the WS background (Apse et al., 2003). In the former study, we showed that epidermal cell expansion, especially that of large highly vacuolated cells, was significantly reduced in the single knockout nhx1, which caused a mild but significant decrease in overall plant growth (Apse et al., 2003). Here we show that the single knockout nhx2 did not exhibit any obvious growth or developmental phenotypes. However, the double knockout nhx1 nhx2 had a more severe reduction in vegetative growth than that of nhx1, and this reduction was associated with a substantial decrease in cell size rather than defects in tissue organization. Our data support the notion that NHX1 and NHX2 might function in a partially redundant manner to control cell expansion.

Roles of NHX1 and NHX2 in Stamen Development and Function

The double knockout nhx1 nhx2 also displayed two distinct floral organ developmental phenotypes, which were not seen in either of the single knockouts, nhx1 or nhx2. The first phenotype was that filaments did not elongate far enough to place anthers at the height of the stigma. Longitudinal sections of filaments indicated that individual filament cells in nhx1 nhx2 were 70% the length of the wild-type cells. The second phenotype was that nhx1 nhx2 anther dehiscence occurred in only 7% of flowers. Together, both phenotypes likely lead to the observed lack of flower set and silique formation in nhx1 nhx2. Given the role of NHX1 in mediating vacuolar K+/H+ exchange (Blumwald and Poole, 1985; Zhang and Blumwald, 2001; Venema et al., 2002; Yamaguchi et al., 2003; Leidi et al., 2010) and the proposed specific role of K+ in filament extension (Heslop-Harrison and Heslop-Harrison, 1996), it is plausible that the reduced cell expansion observed in nhx1 nhx2 filaments might result from a lack of sufficient K+ accumulation in vacuoles of filament cells, which is necessary for osmotic driven cell expansion.

Anther dehiscence is a coordinated process that depends on the active hydration and subsequent dehydration of select anther tissues, including the endothecium and epidermal cells. Hydration directs a turgor-induced force that ultimately ruptures a weakened stomium and causes the opening of the anther locules to expose and release pollen (Scott et al., 2004). Water movement within anthers has been suggested to occur as a consequence of localized accumulation of ions and K+ in particular (Matsui et al., 2000; Rehman and Yun, 2006). A transfer of K+ from the anther locule to pollen grains has also been postulated to cause swelling of pollen grains, which contributes to stomium rupture (Wilson et al., 2011). It is worth noting that we also observed that a significant number of nhx1 nhx2 pollen grains shrunk (Figures 3I and and4G),4G), perhaps because of insufficient swelling.

Here, the stamen phenotypes correlated with filament- and anther-specific expression of NHX1 and NHX2. These observations are supported by available microarray data (Zimmermann et al., 2004) as well as by previous results (Apse et al., 2003). These data also suggest that NHX1 and NHX2 might have specific roles in pollen development and/or pollen tube growth. Recently, it was also shown that two cation/proton exchangers (CHXs) are needed to guide pollen tubes toward the ovule (Lu et al., 2011). However, pollen viability, germination, and reciprocal crossing experiments between the wild-type and nhx1 nhx2 plants suggested that pollen development and its ability to germinate in vitro and in vivo might not be significantly affected in nhx1 nhx2 plants. Thus, it is possible that the roles of CHXs and NHX1 and NHX2 are complementary and that CHXs have both broad and specialized roles in development. Collectively, our data point to a developmentally coordinated role in which NHX1 and NHX2 regulate K+ homeostasis in stamens, and this homeostasis enables filament elongation and anther dehiscence to occur.

Interestingly, when soil-grown nhx1 nhx2 plants were watered with solutions containing 100 mM NaCl, filament elongation and flower set was restored, along with a concomitant and significant increase in silique formation (Figure 6). These results suggest that other vacuolar transporters, possibly NHX3, NHX4, and/or CHXs, are mediating H+-driven Na+ uptake into vacuoles, allowing for osmotic-driven vacuolar expansion to elongate the filament and bypass the specific requirement of K+ accumulation in filament cells.

Regulation of Vacuolar pH and K+ Homeostasis to Control Cell Expansion

The lack of cell expansion and tissue elongation in nhx1 nhx2 plants was not limited to leaves and filaments but was also observed in hypocotyls of etiolated seedlings, in which nhx1 nhx2 hypocotyls were shorter than the wild type. Using seedlings, we measured vacuolar pH and K+ content in hypocotyl and root cell vacuoles and found that in nhx1 nhx2, vacuolar pH was more acidic, and K+ content was only 30% of that in the wild-type cells. These differences were only observed in highly vacuolated cells of the mature root zone and the hypocotyl and not in the nonvacuolated cells of the root tip, suggesting a close relationship between NHX1, NHX2, vacuolar K+ and pH homeostasis, and cell size. Our values for vacuolar pH (5.5) and K+ (75 mM in the wild type) were similar to other reported values obtained using 31P NMR (Martinez and Lauchli, 1993) ion-selective microelectrodes (Walker et al., 1996; Carden et al., 2003; Leidi et al., 2010) and fluorescent dyes (Swanson et al., 1998; Halperin and Lynch, 2003; Krebs et al., 2010). Assuming a cytosolic concentration of 100 mM K+, a tonoplast membrane potential of 30 mV, and steady state with the cytosol, the vacuolar K+ concentration would be ~20 mM and similar to the vacuolar K+ content we measured in nhx1 nhx2 cells. A more acidic pH and significantly lower K+ content of nhx1 nhx2 are consistent with the localization and biochemical function of NHX transporters at the tonoplast.

In the single knockout nhx1, Apse et al. (2003) measured a reduction in K+/H+ and Na+/H+ exchange and, because of this and the reduced cell expansion phenotype of nhx1, proposed that under normal physiological conditions, NHX1 regulates vacuolar K+ and/or pH to control cell expansion. Using NHX1-overexpressing tomatoes, Leidi et al. (2010) concluded that NHX1 overexpression led to increased vacuolar K+ accumulation at the expense of cytosolic K+ depletion, which was correlated with early K+ deficiency symptoms, upregulation of HAK5 expression, and greater K+ uptake compared with the wild type, despite the measurement of higher tissue K+ content in transgenic plants. Our results closely mirror the findings of Leidi et al. (2010) and essentially point to a similar function of NHX1 and NHX2. Under normal growth conditions (i.e., low Na+ concentrations), these two exchangers primarily mediate K+/H+ exchange, as supported by earlier findings (Zhang and Blumwald, 2001; Apse et al., 2003).

Most cellular K+ is located within the vacuole, where it serves as an osmoticum to drive turgor, but significant amounts (80 to 100 mM) also exist in the cytosol, where it is critical for protein function and stability and as an enzyme cofactor (Leigh and Jones, 1984; Amtmann and Leigh, 2010). The vacuolar K+ pool is a main supplier of cytosolic K+, because under varying external K+ concentrations, cytosolic K+ is tightly maintained, whereas the vacuolar K+ pool fluctuates with K+ supply and tissue content (Walker et al., 1996). The data of Walker et al. strongly implied that cytosolic K+ might be maintained in part by exchange with the vacuole, a role that can be satisfied in part by NHX-type antiporters. At the typical tonoplast membrane potential (~30 mV, positive inside), transport of K+ would occur against its potential, which suggests that it must be energized (Martinoia et al., 2000). Our data support this notion. When grown on K+-supplemented media (30 mM), nhx1 nhx2 growth was adversely affected compared with that in normal K+ (1 mM). Given that the electrochemical potential of K+ favors uptake into the cell as well as the lack in K+ vacuolar accumulation, we reason that a high supply of K+ was deleterious to nhx1 nhx2 growth, probably because K+ was accumulating to toxic levels in the cytosol. Although there is significant information on the consequences of limiting K+ uptake at the plasma membrane, little is known about the possible consequences of increasing cytosolic K+ by limiting vacuolar K+ sequestration. In other words, little is known about cellular responses to elevated cytosolic K+. This is probably because when plants are exposed to high external K+ concentrations, changes in cytosolic K+ are efficiently modulated by the compartmentation of K+ into vacuoles (Walker et al., 1996; Leigh, 2001). In this respect, given the low exchange of K+ at the tonoplast in nhx1 nhx2, these plants could serve as a useful tool to study the cellular effects of shifts in cytosolic K+ homeostasis. The adverse response of nhx1 nhx2 plants to high external K+ raises interesting questions about cellular K+ homeostasis and feedback control between vacuole, cytosol, and the extracellular medium. The toxic effects of such relatively low (30 mM) K+ concentration on the nhx1 nhx2 seedlings might also suggest indirect effects on other cellular functions. For example, cytosolic K+ could induce the dephosphorylation of the plasma membrane (H+)–ATPase, downregulating its activity with the concomitant decrease in the transmembrane electrochemical H+ gradient (Buch-Pedersen et al., 2006). These aspects are beyond the scope of this study and require further investigation.

The growth of nhx1 nhx2 plants increased significantly in the presence of moderate amounts of Na+ (30 mM), supporting the notion that Na+ uptake into the vacuole does not depend solely on NHX1 and NHX2 activities, and that Na+ is transported into the vacuole through other transporters. Na+ likely substituted in part for the lack of K+ accumulation in vacuoles, where it induced cell expansion by increasing the osmotic potential and turgor that was probably insufficient in nonsalinized nhx1 nhx2. It is well known that at low K+ conditions, Na+ can partly substitute for K+ in the vacuole and can therefore positively affect growth (Bartels and Sunkar, 2005). At low concentrations (<30 mM NaCl in the case of Arabidosis), Na+ was beneficial to growth, because it probably served as a metabolically cheap osmoticum (Bartels and Sunkar, 2005). Nevertheless, Na+ did not replace the plant’s K+ requirements, because the vegetative and reproductive phenotype of nhx1 nhx2 when grown under added Na+ were not completely rescued.

Increased vacuolar acidification in nhx1 nhx2 would also result in changes in the electrical potential differences across the tonoplast (i.e., depolarization), which could affect the vacuolar H+-pump activity and the activities of other transporters, in particular gated ion channels (Pantoja et al., 1992). A critical role of NHX antiporters in pH regulation is best exemplified by their function in alkalinization of the vacuole during petal development and color transitions in Japanese morning glory (Ipomoea nil) (Yamaguchi et al., 2001; Ohnishi et al., 2005). In addition, NHX1 activity is regulated by a calmodulin-like protein at the C terminus in a Ca2+- and pH-dependent manner. Binding of the calmodulin-like protein to NHX1 decreased the Vmax for Na+/H+ exchange but not for K+/H+ exchange, thereby modulating H+-coupled Na+ or K+ exchange (Yamaguchi et al., 2005). This regulation has important implications under salt stress, in which a low Na+:K+ ratio must be maintained in the cytosol. Given the lower vacuolar pH of nhx1 nhx2, it is possible that the regulation of NHX1 selectivity may be altered, influencing the differential response of nhx1 nhx2 plants to Na+ versus K+. Other roles of vacuolar pH, especially those associated with cell expansion, remain largely unknown but may be linked to vesicular trafficking and membrane fusion (Honsbein et al., 2011).

In summary, NHX1 and NHX2 are vacuolar proteins that control vacuolar pH and K+ homeostasis. We provide evidence to support the role of NHX1 and NHX2 in mediating K+/H+ exchange. This exchange regulates cell expansion in rapidly elongating tissues, such as filaments and hypocotyls, and plays unique and specific roles in flower development.

METHODS

Plant Materials and Growth Conditions

Arabidopsis thaliana (Col-0) were grown in soil at 22°C under diurnal light conditions as specified below. For plate-grown plants, modified Murashige and Skoog media (Spalding et al., 1999), with 1% phytagel (Sigma-Aldrich), no Suc, and pH 5.7. 1 mM Na+ was considered the control Na+ concentration. For Na+ and K+ experiments, media were supplemented with KCl or NaCl as indicated in the figure legends. Plate-grown plants were incubated at 22°C for 12 h light and 12 h dark. For flower analysis, the wild-type and nhx1 nhx2 plants were grown in soil under short days (8 h light), and at 4 weeks, were irrigated with 50 mM NaCl followed by 100 mM NaCl 2 d later. An additional 25 mM NaCl was included once a week with irrigation. At 5 weeks, the plants were switched to long days (16 h light) to induce flowering.

T-DNA insertion mutants (Col-0) (http://signal.salk.edu/cgi-bin/tdnaexpress) for NHX1 were nhx1-1 (SALK_34001) and nhx1-2 (SALK_065623) and for NHX2 were nhx2-1 (SALK_036114) and nhx2-3 (SALK_084844). Positions of T-DNA insertion sites are shown in Supplemental Figure 3 online. RT-PCR confirmed no DNA amplification with allele-specific primers from knockout-derived cDNA. All single knockouts were backcrossed with Col-0 wild-type plants twice, and corresponding lines with single T-DNA insertions were selected by DNA gel blot hybridization using the left border sequence as the probe. Primer sequences for the confirmation of homozygous T-DNA insertions are listed in Supplemental Table 1 online.

Plasmid Construction and Plant Transformation

All of the constructs in this study were generated using the Gateway system (Invitrogen). cDNAs of NHX1 and NHX2 (without stop codons) were cloned into pDONR207 (Invitrogen) to generate entry vectors (pDONR207-NHX1, pDONR207-NHX2) and recombined into pEarleyGate103 for GFP fusion and pEarleyGate101 for YFP fusion (Earley et al., 2006). The constructs were introduced into Arabidopsis Col-0 plants expressing translational fusion proteins, and into nhx1-1 nhx2-1 for complementation by Agrobacterium tumefaciens (GV3101) using the floral dipping method (Clough and Bent, 1998). The Ub10-NHX1-GFP construct was generated using Multisite Gateway method (Invitrogen). 634 bp of Ubiquitin-10 promoter was cloned from pNIGEL07 (Geldner et al., 2009) into pDONRP4P1r (Invitrogen) to generate pDONRL4R1-UBQ10pro as a first fragment entry vector. The pDONRL4R1-UBQ10pro was recombined with the entry vectors pDONR207-NHX1 and pEN-R2-F-L3 into pB7m34GW destination vector (Karimi et al., 2007). For the 35S-NHX2-RFP construct, pDONR207-NHX2 was recombined into pH7RWG2 (Karimi et al., 2007). The Ub10-NHX1-GFP and the 35S-NHX2-RFP were introduced into A. tumefaciens strain EHA105. Those constructs were transiently expressed in cotyledons of the wild-type and VAMP711-RFP Arabidopsis seedlings (Marion et al., 2008). A list of primers is included in Supplemental Table 1 online.

Pollen Viability and Germination

Flowers of the wild type and nhx1 nhx2 were harvested in the morning and used to dust pollen on 2.5% gelatin (from porcine skin; Sigma-Aldrich) solidified on glass plates. To assay pollen viability, several drops of water containing 1 μM DAPI were added to the gelatin pad. Pollen germination was modified from the protocol of (Boavida and McCormick, 2007). Pollen from 50 wild-type flowers and 100 nhx1 nhx2 flowers were collected in a 1.5-mL tube with liquid germination medium (0.01% H3BO3, 5 mM CaCl2, 5 mM KCl, 1 mM MgSO4, 5 mM Tris-MES [pH 7.5], 10% Suc) and vortexed briefly. Pollen was pelleted for 1 min at 13,000 rpm, resuspended in 250 μL fresh pollen germination medium, and transferred to small glass vials with their screw caps loosely attached. Pollen was germinated at 22°C in light for 6 h, without agitation. 50-μL aliquots were used to assess percent germination from defined areas of slides. Pollen germination medium was always made fresh from stock solutions. For reciprocal crosses, flowers were emasculated at night 18 to 20 h before cross-pollination. Given the slower development of nhx1 nhx2 flowers, and to ensure that all flowers were at the same developmental stage, nhx1 nhx2 flowers used for crosses were ~20 h older than the wild-type flowers.

Histological Analysis

Preparation of plant tissues was performed as previously reported (Bassil et al., 2011). Briefly, tissue was fixed in formalin–acetic acid–alcohol, under vacuum, rinsed, and dehydrated in a graded series of ethanol before being mixed with xylenes and paraffin and sectioned. Serial sections were stained with periodic acid–Schiff for total carbohydrates and were counterstained with amido black 10B for protein or toluidine blue O for general histological organization.

Fluorescence and Light Microscopy

Fluorescence microscopy was performed using a Leica confocal laser-scanning microscope (DM RXE 6 TCS-SP2 AOBS) equipped with a 63× water immersion objective. The excitation wavelength was 488 nm for GFP and 594 nm for RFP, and emission was 500 to 535 nm for GFP and 600 to 660 for RFP. To avoid crosstalk between fluorescence channels, sequential scanning was used when necessary. Images were processed with ImageJ (http://rsbweb.nih.gov/ij/).

Electron Microscopy

Mature flowers were partly dissected to expose floral organs before fixation (2.5% paraformaldehyde, 2.0% glutaraldehyde in 0.08 M sodium phosphate buffer, pH 7.2) under vacuum (1 h) and were rinsed with 0.1 M sodium phosphate buffer. Tissue was then dehydrated in ascending concentrations of ethyl alcohol (30, 50, 70, 95, and 100%), then dried in a critical point dryer, mounted onto aluminum stubs, and coated with gold. Flowers were viewed with a scanning electron microscope using 20 kV (Philips XL30 TMP; FEI) at the University of California, Davis (Electron Microscopy Laboratory, Department of Pathology and Laboratory Medicine, School of Medicine).

Measurement of Vacuolar K+ and pH

Vacuolar pH was measured using the pH-sensitive dye BCECF-AM in root and hypocotyls cells of 5-d-old seedlings grown on vertical plates. Dye loading was performed as described by Krebs et al. (2010) with minor modifications. Briefly, seedlings were incubated in 1/10 Murashige and Skoog liquid medium (0.5% Suc, 10 mM MES, pH 5.7) containing 10 μM BCECF-AM 0.02% pluronic F-127 (Molecular Probes) for 1 h in darkness at 22°C and were washed twice before microscopy. Dye fluorescence images were collected using a Leica confocal laser-scanning microscope (DM RXE 6 TCS-SP2 AOBS) equipped with a 20× objective after excitation with 458 and 488 nm. Single emission between 525 and 550 nm was collected for each excitation wavelength. Images were collected from root tip cells, mature root cells of the elongation zone, and hypocotyls cells. After background correction, the integrated pixel intensity was measured for both the 458 nm-excited images and the 488 nm-excited images, and ratios were calculated (ImageJ v1.43; National Institutes of Health). Fluorescence ratio values were used to calculate the pH from a calibration curve. For pH calibration, seedlings were equilibrated 15 min before observation in equilibration buffer containing 50 mM BTP-HEPES or MES (pH 5.0 to 7.4) and 50 mM ammonium acetate. For each ratio value, 10 images from each of 25 seedlings were measured, and the experiment was repeated at least five times.

For determination of vacuolar K+, the ratiometric dye PBFI-AM (Molecular Probes) procedure (Halperin and Lynch, 2003) was used with slight modifications. PBFI-AM was loaded into 5-d-old seedlings as described for BCECF-AM above, except that 20 μM and 18 h of loading were used. Images above 500 nm emission were collected when roots and hypocotyls were excited with 360 nm and 380 nm, respectively, using an Hg lamp source fitted to a Leica DMRE running MetaMorph v7.1 (Molecular Devices). In situ calibration of vacuolar K+ was performed by incubating dye-loaded tissue with 2 μM gramicidin in dye-loading buffer and concentrations of KCl (0 to 100 mM) to generate a standard curve of fluorescence ratio (Halperin and Lynch, 2003). There is an inherent difficulty in buffering K+ near zero when performing in vivo calibrations, but this was not a significant limitation, because all measured values fell within the calibration range (i.e., ratios corresponding to 15 mM and above). Images were corrected for background fluorescence as described for BCECF-AM.

Leaf Ion Contents

The samples were weighed and digested in ~3 mL of 3:1 HNO3:H2O2 for 24 h. An aliquot of the digest was diluted 30-fold with 3% HNO3 and was measured with inductively coupled plasma atomic emission spectroscopy.

RNA Preparation and Expression Analysis

Total RNA was extracted from rosette leaves using RNeasy Mini kit (Qiagen) with six biological replicates, treated with DNaseI, and subsequently purified with RNeasy RNA purification column (Qiagen). First-strand cDNA was synthesized from 1 μg of total RNA with the QuantiTect Reverse Transcription Kit (Qiagen). Primer Express (Applied Biosystem, Life Technologies) was used to design primers. Quantitative PCR (qPCR) was performed on the StepOnePlus (Applied Biosystems) using SYBR GREEN (Bio–Rad). The reaction volume included 2 μL template, 0.3 μL of reverse primer, 0.3 μL of forward primer, 7.5 μL SYBR Green Master Mix, and 4.9 μL RNA-free water (total 15 μL). qPCR was performed as follows: 95°C for 10 min followed by 40 cycles of 95°C for 30 s and 60°C for 30 s. The cycle threshold (CT) 2−ΔΔCT method (Livak and Schmittgen, 2001) was used to determine the relative mRNA using PP2A as an internal reference, because PP2A was previously found to express similarly in all genotypes and organs examined here (Bassil et al., 2011). Primer sequences for RT-PCR and qPCR are listed in Supplemental Table 1 online.

Accession Numbers

Sequence data from this article can be found in the Arabidopsis Genome Initiative database under the following accession numbers: NHX1 (At5g27150) and NHX2 (At3g05030).

Supplemental Data

The following materials are available in the online version of this article.

Acknowledgments

We thank Martin Kottackal, Zvi Peleg, Carla A. Delatorre, Yuval Cohen, and Monica Aladente-Saez for helpful discussions and Pat Kysar for assistance with electron microscopy. We thank the Salk Institute Genomic Analysis Laboratory for generating the sequence-indexed Arabidopsis T-DNA insertion mutants and the ABRC for proving them. This work was supported in part by grants from the National Science Foundation (MCB-0343279; IOS-0820112) and the Will W. Lester Endowment, University of California, to E. Blumwald.

AUTHOR CONTRIBUTIONS

E. Bassil and E. Blumwald designed the research. E. Bassil, H.T., Y.-C.L., M.O., T.E., K.U., R.N., A.C., and M.B. performed the research. E. Bassil and E. Blumwald wrote the article.

References

  • Aharon G.S., Apse M.P., Duan S., Hua X., Blumwald E. (2003). Characterization of a family of vacuolar Na+/H+ antiporters in Arabidopsis thaliana. Plant Soil 253: 245–256
  • Alandete-Saez M., Ron M., McCormick S. (2008). GEX3, expressed in the male gametophyte and in the egg cell of Arabidopsis thaliana, is essential for micropylar pollen tube guidance and plays a role during early embryogenesis. Molecular Plant 1: 586–598 [PubMed]
  • Amtmann A., Leigh R. (2010). Ion homeostasis. Abiotic Stress Adaptation in Plants, Pareek A., Sopory S.K., Bohnert H.J., editors. , (Dordrecht, The Netherlands: Springer; ), pp. 245–262
  • Apse M.P., Blumwald E. (2007). Na+ transport in plants. FEBS Lett. 581: 2247–2254 [PubMed]
  • Apse M.P., Sottosanto J.B., Blumwald E. (2003). Vacuolar cation/H+ exchange, ion homeostasis, and leaf development are altered in a T-DNA insertional mutant of AtNHX1, the Arabidopsis vacuolar Na+/H+ antiporter. Plant J. 36: 229–239 [PubMed]
  • Apse M.P., Aharon G.S., Snedden W.A., Blumwald E. (1999). Salt tolerance conferred by overexpression of a vacuolar Na+/H+ antiport in Arabidopsis. Science 285: 1256–1258 [PubMed]
  • Bartels D., Sunkar R. (2005). Drought and salt tolerance in plants. Crit. Rev. Plant Sci. 24: 23–58
  • Bassil E., Ohto M.A., Esumi T., Tajima H., Zhu Z., Cagnac O., Belmonte M., Peleg Z., Yamaguchi T., Blumwald E. (2011). The Arabidopsis intracellular Na+/H+ antiporters NHX5 and NHX6 are endosome associated and necessary for plant growth and development. Plant Cell 23: 224–239 [PMC free article] [PubMed]
  • Blumwald E. (1987). Tonoplast vescicles as a tool in the study of ion-transport at the plant vacuole. Physiol. Plant. 69: 731–734
  • Blumwald E., Poole R.J. (1985). Na+/H+ antiport in isolated tonoplast vesicles from storage tissue of Beta vulgaris. Plant Physiol. 78: 163–167 [PMC free article] [PubMed]
  • Boavida L.C., McCormick S. (2007). Temperature as a determinant factor for increased and reproducible in vitro pollen germination in Arabidopsis thaliana. Plant J. 52: 570–582 [PubMed]
  • Bowers K., Levi B.P., Patel F.I., Stevens T.H. (2000). The sodium/proton exchanger Nhx1p is required for endosomal protein trafficking in the yeast Saccharomyces cerevisiae. Mol. Biol. Cell 11: 4277–4294 [PMC free article] [PubMed]
  • Brett C.L., Donowitz M., Rao R. (2005a). Evolutionary origins of eukaryotic sodium/proton exchangers. Am. J. Physiol. Cell Physiol. 288: C223–C239 [PubMed]
  • Brett C.L., Tukaye D.N., Mukherjee S., Rao R.J. (2005b). The yeast endosomal Na+(K+)/H+ exchanger Nhx1 regulates cellular pH to control vesicle trafficking. Mol. Biol. Cell 16: 1396–1405 [PMC free article] [PubMed]
  • Buch-Pedersen M.J., Rudashevskaya E.L., Berner T.S., Venema K., Palmgren M.G. (2006). Potassium as an intrinsic uncoupler of the plasma membrane H+-ATPase. J. Biol. Chem. 281: 38285–38292 [PubMed]
  • Carden D.E., Walker D.J., Flowers T.J., Miller A.J. (2003). Single-cell measurements of the contributions of cytosolic Na+ and K+ to salt tolerance. Plant Physiol. 131: 676–683 [PMC free article] [PubMed]
  • Clough S.J., Bent A.F. (1998). Floral dip: A simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 16: 735–743 [PubMed]
  • Earley K.W., Haag J.R., Pontes O., Opper K., Juehne T., Song K., Pikaard C.S. (2006). Gateway-compatible vectors for plant functional genomics and proteomics. Plant J. 45: 616–629 [PubMed]
  • Geldner N., Denervaud-Tendon V., Hyman D.L., Mayer U., Stierhof Y.D., Chory J. (2009). Rapid, combinatorial analysis of membrane compartments in intact plants with a multicolor marker set. Plant J. 59: 169–178 [PubMed]
  • Grefen C., Donald N., Hashimoto K., Kudla J., Schumacher K., Blatt M.R. (2010). A ubiquitin-10 promoter-based vector set for fluorescent protein tagging facilitates temporal stability and native protein distribution in transient and stable expression studies. Plant J. 64: 355–365 [PubMed]
  • Halperin S.J., Lynch J.P. (2003). Effects of salinity on cytosolic Na+ and K+ in root hairs of Arabidopsis thaliana: In vivo measurements using the fluorescent dyes SBFI and PBFI. J. Exp. Bot. 54: 2035–2043 [PubMed]
  • Hamaji K., et al. (2009). Dynamic aspects of ion accumulation by vesicle traffic under salt stress in Arabidopsis. Plant Cell Physiol. 50: 2023–2033 [PubMed]
  • Hernandez A., Jiang X.Y., Cubero B., Nieto P.M., Bressan R.A., Hasegawa P.M., Pardo J.M. (2009). Mutants of the Arabidopsis thaliana cation/H+ antiporter AtNHX1 conferring increased salt tolerance in yeast. The endosome/prevacuolar compartment is a target for salt toxicity. J. Biol. Chem. 284: 14276–14285 [PMC free article] [PubMed]
  • Heslop-Harrison Y., Heslop-Harrison J.S. (1996). Lodicule function and filament extension in the grasses: Potassium ion movement and tissue specialization. Ann. Bot. (Lond.) 77: 573–582
  • Honsbein A., Blatt M.R., Grefen C. (2011). A molecular framework for coupling cellular volume and osmotic solute transport control. J. Exp. Bot. 62: 2363–2370 [PubMed]
  • Karimi M., Bleys A., Vanderhaeghen R., Hilson P. (2007). Building blocks for plant gene assembly. Plant Physiol. 145: 1183–1191 [PMC free article] [PubMed]
  • Krebs M., Beyhl D., Gorlich E., Al-Rasheid K.A.S., Marten I., Stierhof Y.D., Hedrich R., Schumacher K. (2010). Arabidopsis V-ATPase activity at the tonoplast is required for efficient nutrient storage but not for sodium accumulation. Proc. Natl. Acad. Sci. USA 107: 3251–3256 [PMC free article] [PubMed]
  • Leidi E.O., Barragan V., Rubio L., El-Hamdaoui A., Ruiz M.T., Cubero B., Fernandez J.A., Bressan R.A., Hasegawa P.M., Quintero F.J., Pardo J.M. (2010). The AtNHX1 exchanger mediates potassium compartmentation in vacuoles of transgenic tomato. Plant J. 61: 495–506 [PubMed]
  • Leigh R.A. (2001). Potassium homeostasis and membrane transport. J. Plant Nutr. Soil Sci. 164: 193–198
  • Leigh R.A., Jones R.G.W. (1984). A hypothesis relating critical potassium concentrations for growth to the distribution and functions of this ion in the plant-cell. New Phytol. 97: 1–13
  • Livak K.J., Schmittgen T.D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25: 402–408 [PubMed]
  • Lu Y., Chanroj S., Zulkifli L., Johnson M.A., Uozumi N., Cheung A., Sze H. (2011). Pollen tubes lacking a pair of K+ transporters fail to target ovules in Arabidopsis. Plant Cell 23: 81–93 [PMC free article] [PubMed]
  • Marion J., Bach L., Bellec Y., Meyer C., Gissot L., Faure J.D. (2008). Systematic analysis of protein subcellular localization and interaction using high-throughput transient transformation of Arabidopsis seedlings. Plant J. 56: 169–179 [PubMed]
  • Martinez V., Lauchli A. (1993). Effects of Ca2+ on the salt-stress response of barley roots as observed by in-vivo P-31-nuclear magnetic-resonance and in-vitro analysis. Planta 190: 519–524
  • Martinoia E., Massonneau A., Frangne N. (2000). Transport processes of solutes across the vacuolar membrane of higher plants. Plant Cell Physiol. 41: 1175–1186 [PubMed]
  • Martinoia E., Maeshima M., Neuhaus H.E. (2007). Vacuolar transporters and their essential role in plant metabolism. J. Exp. Bot. 58: 83–102 [PubMed]
  • Maser P., et al. (2001). Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol. 126: 1646–1667 [PMC free article] [PubMed]
  • Matsui T., Omasa K., Horie T. (2000). High temperature at flowering inhibits swelling of pollen grains, a driving force for thecae dehiscence in rice (Oryza sativa L.). Plant Prod. Sci. 3: 430–434
  • Ohnishi M., Fukada-Tanaka S., Hoshino A., Takada J., Inagaki Y., Iida S. (2005). Characterization of a novel Na+/H+ antiporter gene InNHX2 and comparison of InNHX2 with InNHX1, which is responsible for blue flower coloration by increasing the vacuolar pH in the Japanese morning glory. Plant Cell Physiol. 46: 259–267 [PubMed]
  • Pantoja O., Gelli A., Blumwald E. (1992). Characterization of vacuolar malate and K+ channels under physiological conditions. Plant Physiol. 100: 1137–1141 [PMC free article] [PubMed]
  • Pardo J.M., Cubero B., Leidi E.O., Quintero F.J. (2006). Alkali cation exchangers: Roles in cellular homeostasis and stress tolerance. J. Exp. Bot. 57: 1181–1199 [PubMed]
  • Rehman S., Yun S.J. (2006). Developmental regulation of K accumulation in pollen, anthers, and papillae: Are anther dehiscence, papillae hydration, and pollen swelling leading to pollination and fertilization in barley (Hordeum vulgare L.) regulated by changes in K concentration? J. Exp. Bot. 57: 1315–1321 [PubMed]
  • Rodriguez-Rosales M.P., Jiang X.Y., Galvez F.J., Aranda M.N., Cubero B., Venema K. (2008). Overexpression of the tomato K+/H+ antiporter LeNHX2 confers salt tolerance by improving potassium compartmentalization. New Phytol. 179: 366–377 [PubMed]
  • Rodriguez-Rosales M.P., Galvez F.J., Huertas R., Aranda M.N., Baghour M., Cagnac O., Venema K. (2009). Plant NHX cation/proton antiporters. Plant Signal. Behav. 4: 265–276 [PMC free article] [PubMed]
  • Scott R.J., Spielman M., Dickinson H.G. (2004). Stamen structure and function. Plant Cell 16: S46–S60 [PMC free article] [PubMed]
  • Shi H., Ishitani M., Kim C., Zhu J.-K. (2000). The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter. Proc. Natl. Acad. Sci. USA 97: 6896–6901 [PMC free article] [PubMed]
  • Sottosanto J.B., Gelli A., Blumwald E. (2004). DNA array analyses of Arabidopsis thaliana lacking a vacuolar Na+/H+ antiporter: Impact of AtNHX1 on gene expression. Plant J. 40: 752–771 [PubMed]
  • Spalding E.P., Hirsch R.E., Lewis D.R., Qi Z., Sussman M.R., Lewis B.D. (1999). Potassium uptake supporting plant growth in the absence of AKT1 channel activity: Inhibition by ammonium and stimulation by sodium. J. Gen. Physiol. 113: 909–918 [PMC free article] [PubMed]
  • Swanson S.J., Bethke P.C., Jones R.L. (1998). Barley aleurone cells contain two types of vacuoles: Characterization of lytic organelles by use of fluorescent probes. Plant Cell 10: 685–698 [PMC free article] [PubMed]
  • Uemura T., Ueda T., Ohniwa R.L., Nakano A., Takeyasu K., Sato M.H. (2004). Systematic analysis of SNARE molecules in Arabidopsis: Dissection of the post-Golgi network in plant cells. Cell Struct. Funct. 29: 49–65 [PubMed]
  • Venema K., Quintero F.J., Pardo J.M., Donaire J.P. (2002). The Arabidopsis Na+/H+ exchanger AtNHX1 catalyzes low affinity Na+ and K+ transport in reconstituted liposomes. J. Biol. Chem. 277: 2413–2418 [PubMed]
  • Venema K., Belver A., Marin-Manzano M.C., Rodriguez-Rosales M.P., Donaire J.P. (2003). A novel intracellular K+/H+ antiporter related to Na+/H+ antiporters is important for K+ ion homeostasis in plants. J. Biol. Chem. 278: 22453–22459 [PubMed]
  • Walker D.J., Leigh R.A., Miller A.J. (1996). Potassium homeostasis in vacuolate plant cells. Proc. Natl. Acad. Sci. USA 93: 10510–10514 [PMC free article] [PubMed]
  • Wilson Z.A., Song J., Taylor B., Yang C. (2011). The final split: The regulation of anther dehiscence. J. Exp. Bot. 62: 1633–1649 [PubMed]
  • Yamaguchi T., Apse M.P., Shi H.Z., Blumwald E. (2003). Topological analysis of a plant vacuolar Na+/H+ antiporter reveals a luminal C terminus that regulates antiporter cation selectivity. Proc. Natl. Acad. Sci. USA 100: 12510–12515 [PMC free article] [PubMed]
  • Yamaguchi T., Aharon G.S., Sottosanto J.B., Blumwald E. (2005). Vacuolar Na+/H+ antiporter cation selectivity is regulated by calmodulin from within the vacuole in a Ca2+- and pH-dependent manner. Proc. Natl. Acad. Sci. USA 102: 16107–16112 [PMC free article] [PubMed]
  • Yamaguchi T., Fukada-Tanaka S., Inagaki Y., Saito N., Yonekura-Sakakibara K., Tanaka Y., Kusumi T., Iida S. (2001). Genes encoding the vacuolar Na+/H+ exchanger and flower coloration. Plant Cell Physiol. 42: 451–461 [PubMed]
  • Yokoi S., Quintero F.J., Cubero B., Ruiz M.T., Bressan R.A., Hasegawa P.M., Pardo J.M. (2002). Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response. Plant J. 30: 529–539 [PubMed]
  • Yoshida K., Miki N., Momonoi K., Kawachi M., Katou K., Okazaki Y., Uozumi N., Maeshima M., Kondo T. (2009). Synchrony between flower opening and petal-color change from red to blue in morning glory, Ipomoea tricolor cv. Heavenly Blue. Proc. Jpn. Acad. Ser. B Phys. Biol. Sci. 85: 187–197 [PMC free article] [PubMed]
  • Zhang H.X., Blumwald E. (2001). Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit. Nat. Biotechnol. 19: 765–768 [PubMed]
  • Zimmermann P., Hirsch-Hoffmann M., Hennig L., Gruissem W. (2004). GENEVESTIGATOR. Arabidopsis Microarray Database and Analysis Toolbox. Plant Physiol. 136: 2621–2632 [PMC free article] [PubMed]

Articles from The Plant Cell are provided here courtesy of American Society of Plant Biologists
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links