Cation/H+ exchangers encoded by CAX genes play an important role in the vacuolar accumulation of metals including Ca2+ and Mn2+. Arabidopsis thaliana CAX1 and CAX3 have been previously shown to differ phylogenetically from CAX2 but the physiological roles of these different transporters are still unclear. To examine the functions and the potential of redundancy between these three cation transporters, cax1/cax2 and cax2/cax3 double knockout mutants were generated and compared with wild type and cax single knockouts. These double mutants had equivalent metal stress responses to single cax mutants. Both cax1 and cax1/cax2 had increased tolerance to Mg stress, while cax2 and cax2/cax3 both had increased sensitivity to Mn stress. The cax1/cax2 and cax2/cax3 mutants did not exhibit the deleterious developmental phenotypes previously seen with the cax1/cax3 mutant. However, these new double mutants did show alterations in seed germination, specifically a delay in germination time. These alterations correlated with changes in nutrient content within the seeds of the mutants, particularly the cax1/cax2 mutant which had significantly higher seed content of Ca and Mn. This study indicates that the presence of these Arabidopsis CAX transporters is important for normal germination and infers a role for CAX proteins in metal homeostasis within the seed.
Citation: Connorton JM, Webster RE, Cheng N, Pittman JK (2012) Knockout of Multiple Arabidopsis Cation/H+ Exchangers Suggests Isoform-Specific Roles in Metal Stress Response, Germination and Seed Mineral Nutrition. PLoS ONE 7(10): e47455. doi:10.1371/journal.pone.0047455
Editor: Ivan Baxter, United States Department of Agriculture, Agricultural Research Service, United States of America
Received: May 26, 2012; Accepted: September 17, 2012; Published: October 12, 2012
Copyright: © Connorton et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by a Biotechnology and Biological Sciences Research Council (BBSRC) David Phillips Fellowship grant (BB/B502152/1) to J.K.P., a BBSRC PhD studentship for J.M.C., and funding from The United States Department of Agriculture/Agricultural Research Service under Cooperation Agreement 6250-51000-055 to N.C. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Metal transporters play a major role in regulating metal homeostasis, in controlling the acquisition of essential metal nutrients into the plant, coordinating the distribution and partitioning of these nutrients to appropriate locations within the plant and within individual cells, and preventing or responding to metal toxicity . Studies of metal homeostasis over a number of years in model species like Arabidopsis thaliana, has led to the genetic identification of many metal transporters, a few of which have been characterised and understood in specific detail, but many of which are still poorly understood in terms of biochemical and/or physiological function –. In addition, far less is understood about the potential interactions and cross talk between metal transporters, and the influence that changes in one metal through the action of a specific transporter, have on the ionome, which defines the elemental composition of the whole organism .
CAX (cation/H+ exchanger) genes encode a family of important vacuolar-localised metal transporters that function as cation/H+ exchangers . They mediate the high capacity sequestration of cations into the vacuole and are energised by the counter flux of H+ and thus utilise the large proton electrochemical gradient which exists across the tonoplast. The central vacuole of plant cells appears to be an important organelle for the regulation of metal homeostasis, both as a critical sub-cellular sink for providing metal tolerance and as an important source for bioavailable metals, such as during nutrient deficiency or for the propagation of Ca2+ signals –. Ca2+ transport is thought to be a major role of the plant CAX transporters, and all plant CAX genes examined to date have the ability to transport Ca2+ , . Through the analysis of CAX mutants, vacuolar Ca2+/H+ exchange activity has been demonstrated to be a critical component in the maintenance of Ca nutrition. For example, knockout of Arabidopsis vacuolar Ca2+/H+ exchangers (CAX1 and CAX3) can cause sensitivity to elevated Ca and other developmental phenotypes including reduced growth and inhibited stomatal function due to an inability of mesophyll cells to maintain low apoplastic Ca , . In addition to a nutritional role, Ca2+ is critical for cellular signalling and has been shown to be required to mediate signalling events in response to abiotic and biotic stresses, and during development , . Impaired hormone and developmental responses or abiotic stress phenotypes following deletion of Arabidopsis CAX genes such as CAX1 and CAX3, therefore indicate Ca2+ signalling roles for these vacuolar Ca2+ transporters , –.
Two of the six Arabidopsis CAX genes, CAX1 and CAX3, are particularly important for Ca2+ transport and homeostasis. CAX1 alone accounts for a significant proportion of the total vacuolar Ca2+/H+ transport activity  but when CAX1 is knocked out along with the most closely related gene CAX3 (cax1/cax3 mutant), the resulting plant is extremely sensitive to elevated Ca stress and has a very severe stunted phenotype . However, single knockout mutants associated with these genes do not display such dramatic phenotypes, and it is not fully clear whether the phenotypes associated with the cax1 and cax3 mutants are solely due to impaired Ca homeostasis. Analysis of CAX proteins by heterologous expression has demonstrated that in addition to Ca2+, different CAX isoforms can transport other transition metals –. For example, Arabidopsis CAX2 can transport Cd2+, Mn2+, and Zn2+ when expressed either in yeast or tobacco , , while a cax2 knockout has a significant reduction in vacuolar Mn2+ sequestration compared to wild type, but has no significant change in Ca2+ sequestration . CAX1 and CAX3 may also be able to transport the monovalent cations Na+ and Li+  while a cax3 knockout has increased sensitivity to elevated concentrations of these ions . In addition, expression of the CAX1 open reading frame in yeast found that it also has the ability to transport Mn2+ . Other changes in metal sensitivity and content in CAX mutant plants appear to be due to indirect effects. For example, deletion of CAX1 has been linked with an increased tolerance to Mg stress ,  that is not due to a direct Mg2+ transport by CAX1 but possibly due to the relationship between Ca and Mg in plants . Deletion of CAX1 and CAX3 also gives rise to changes in inorganic phosphate (Pi) mobilisation within the plant which is thought to be due to alterations in CAX-mediated signalling controlling Pi homeostasis .
Phylogenetic analyses have demonstrated that higher plant CAX genes are divided into two sub-groups, named Type 1-A and Type 1-B , . Arabidopsis CAX1, CAX3 and CAX4 are grouped within Type 1-A, while CAX2, CAX5 and CAX6 are within Type 1-B. The relevance of these distinct groupings is unclear and so far, no clear-cut functional differences between the Type 1-A and Type 1-B CAX genes have been determined. The generation of the cax1/cax3 double knockout mutant has allowed the examination of the genetic interactions, isoform specificity and redundancy of CAX transporters within the Type 1-A sub-group , , , but the potential interactions and possibility of redundancy by CAX genes between the Type 1-A and Type 1-B sub-groups have yet to be explored. To address this, cax1/cax2 and cax2/cax3 double knockout mutants have been generated in this study and were phenotypically compared alongside the cax1, cax2 and cax3 single mutants and wild type Arabidopsis plants under non-stressed and metal stress conditions. CAX1, CAX2 and CAX3 genes are known to be expressed in Arabidopsis seed  and it has recently been indicated that CAX transporters are involved in determining metal partitioning within the seed , but the physiological consequence of altered seed metal content following CAX mutation has not previously been studied. Seed germination was therefore quantified in the single and double CAX mutant plants. We describe that cax1/cax2 and cax2/cax3 double mutants have alterations in seed germination compared to wild type and single mutants, specifically a delay in germination time, which correlate with changes in metal content within the seeds of the mutants.
Materials and Methods
Plant materials and generation of cax1/cax2 and cax2/cax3 knockout lines
The Arabidopsis thaliana ecotype Columbia-0 (Col-0) was used for all experiments. Homozygous T-DNA insertion knockout lines cax1-1 , cax2-2 , cax3-1 and cax1/cax3  were all in the Col-0 background. The cax1/cax2 and cax2/cax3 double knockout lines were generated by the crossing of the cax1-1 and cax2-2 alleles, and by the crossing of the cax2-2 and cax3-1 alleles, respectively, and the F2 generations were selected for double mutants. Homozygous double mutant alleles were identified by PCR using oligonucleotide primers generated previously for the selection of single homozygous mutants , ,  and the knockout mutations were confirmed by real-time PCR gene expression analysis (Figure 1).
Changes in CAX expression in cax1, cax2 and cax3 single and double knockout lines relative to Col-0 (wild type) were determined by real-time PCR using actin and ubiquitin as constitutive control primers. RNA was extracted from whole seedling tissue grown on 0.5×MS plates without additional metal supplementation for 21 d. Expression relative to actin is shown and expression relative to ubiquitin was equivalent. Relative fold changes in gene expression were calculated using the 2−ΔΔCt method. Bars indicate the mean log expression±SE from three samples each replicated twice. ‘n’ denotes no increase in expression detected.
Plant growth conditions
Wild type and mutant Arabidopsis were sown onto damp compost (William Sinclair Horticultural) in 9 cm diameter pots and placed in an environmental growth chamber (Percival Scientific) at 22°C with constant light, 160 µE m−2 s−1 light intensity, and controlled 70% relative humidity. For growth on solid media, seeds were surface sterilized with 90% (v/v) ethanol/30% (v/v) sodium hypochlorite then washed five times in Milli-Q water (Millipore) before plating on half-strength Murashige and Skoog (0.5×MS) basal medium (Duchefa) without sucrose, adjusted to pH 5.6 and containing 1% (w/v) agar, with or without added metal salts (25 mM CaCl2, 10 µM CdCl2, 10 mM LiCl, 50 mM NaCl, 25 mM MgCl2, or 1.5 mM MnCl2). Seeds were stratified for 2 d in the dark at 4°C before growth in an environmental growth chamber (Sanyo) at 22°C with a 16 h light/8 h dark cycle, 160 µE m−2 s−1 light intensity. For metal stress and fresh weight analysis, seedlings were grown following germination for 21 d. Entire seedlings were removed, blotted on tissue paper to remove excess water and weighed on a calibrated fine balance (Sartorius).
Arabidopsis seedlings were grown for 18 d on 0.5×MS plates supplemented with metals as described above. Shoot tissue was dissected from the seedling and fresh weight was determined. This was then ground on ice in 80% (v/v) acetone and centrifuged at 13 000×g for 5 min. The supernatant was recovered and the absorbance was measured at 647 nm, 664 nm and 750 nm. Total chlorophyll (chl a+b) content was determined using the equation: chl a+b (µg ml−1) = (17.76×A647 nm−750 nm)+(7.34×A664 nm−750 nm), as described by Porra et al.  and converted on the basis of fresh weight of tissue.
Seeds were combined from at least six homozygous parent plants and wild type plants, harvested at the same time and stored at room temperature for 3 months before sowing. Seeds from different lines of Arabidopsis were harvested at the same time and then sterilely sown onto 1% (w/v) agar (plant cell culture grade, Sigma-Aldrich, A7921) plates in a grid formation (approximately 60 per plate) and sealed with micropore tape. Seeds were stratified for 2 d in the dark at 4°C and then transferred to an incubator at 22°C with a 16 h light/8 h dark cycle. Seeds were left for 9 h and then observed every 2 h under a dissection microscope. Germination was scored using radicle protrusion from the seed coat as an indicator. The mean time to germinate or establish was determined by the equation: Σ(NtT) = /Σn, as described by Bewley and Black , where Nt is the number of seeds germinated or established at each time point, T is the time point, and n is the total number of seeds. Seeds were left for 10 d and any that had not germinated in this period were determined to be non-viable.
Real-time PCR analysis
Total RNA was extracted from Arabidopsis whole seedling tissue (three biological replicates of each line) grown on 0.5×MS plates without additional metal supplementation for 21 d as described above, using a Qiagen plant RNA extraction kit (Qiagen). DNase treated-RNA was converted to cDNA using Superscript III (Invitrogen) reverse transcriptase and an oligo(dT) primer. CAX1, CAX2 and CAX3 gene expression was determined by quantitative real-time PCR using a SYBR Green core qPCR kit (Eurogentec) and an ABI Prism 7000 machine (Applied Biosystems) using the SYBR Green detection program and normalised to actin ACT2 and ubiquitin UBC1 gene expression using primers QACT8L 5′-TGCAGACCGTATGAGCAAAG-3′, QACT8R 5′-CTGGAAAGTGCTGAGGGAAG-3′, QUBC1L 5′-TACCTCCATCCAGTCCTTGC-3′ and QUBC1R 5′-GCTCAACAACATCACGCACT-3′. Primers used for CAX gene expression were QCAX1L 5′-TCGCTGCTAGGTTCGATTTT-3′, QCAX1R 5′-GGCAGCAAGTGACACAAGAA-3′, QCAX2L 5′-TTGCCATGAAAGACAAGCTG-3′, QCAX2R 5′-CCGTCTCAAAAAGCTGGAAG-3′, QCAX3L 5′-GCGTTGGCCAATAACAAAGT-3′ and QCAX3R 5′-GGCGATACCACCAAAGAAGA-3′. Reactions were run in triplicate and PCR efficiencies checked using LinRegPCR . Melting curves were produced for each experiment to ensure that single products were amplified. Fold change in gene expression in mutant lines was determined using the 2−ΔΔCT method where ΔΔCT = (CT target gene−CT reference gene)transgenic line−(CT target gene−CT reference gene)Col-0, as described .
Metal content analysis
Arabidopsis leaves (from 4-week old plants) and seeds from plants grown on soil as described above without additional metal supplementation, were harvested for determination of metal content and oven dried at 60°C for 24 h. Approximately 15 mg dry weight per sample of leaf and seed material was then digested in 0.5 ml of ultra-pure concentrated nitric acid (67%) at 100°C for 3 h. Samples were diluted in Milli-Q water (Millipore) and analysed by inductively coupled plasma atomic emission spectroscopy (ICP-AES) (Perkin-Elmer Optima 5300) and calibrated using an internal standard solution, which was a matrix matched serial dilution of Specpure multi element plasma standard solution 4 (Alfa Aesae).
Vacuolar-enriched membrane vesicle preparation, and proton and metal transport measurements
Vacuolar-enriched membrane vesicles were isolated from 2 week old Arabidopsis seedlings grown on 0.5×MS media, as described above. The seedlings were pre-treated with 50 mM CaCl2 and 1.5 mM MnCl2 14 h before harvest. The procedure for plant tissue homogenisation in a mortar and pestle and preparation of microsomal membrane vesicles was as described previously , then vacuolar-enriched membrane vesicles were prepared following purification of microsomal vesicles through a two-step 22% (w/w) and 34% (w/w) sucrose gradient as described previously . Membrane vesicle purity was determined by measuring ATPase and pyrophosphatase (PPase) hydrolytic activity in the presence of inhibitors of the tonoplast V-type H+-ATPase (V-ATPase), tonoplast K+-dependent H+-PPase, plasma membrane H+-ATPase and mitochondrial H+-ATPase, essentially as described previously , . Tonoplast and mitochondrial ATPase activity was determined in the presence of 40 mM Tris-MES (pH 8.0), 50 mM KCl, 2 mM MgSO4, and 2 mM ATP, while plasma membrane ATPase activity was determined under the same conditions at pH 6.5. Tonoplast PPase activity was determined in the presence of 40 mM Tris-MES (pH 8.0), 50 mM KCl, 5 mM MgSO4, and 0.1 mM sodium pyrophosphate. The following inhibitors were used: 100 µM sodium orthovanadate (plasma membrane H+-ATPase inhibitor), 50 mM potassium nitrate and 0.2 µM bafilomycin (both tonoplast V-ATPase inhibitors), and 1 mM sodium azide (mitochondrial ATPase inhibitor). The absence of KCl was used as an inhibitor of tonoplast PPase activity. Fifty µl of tonoplast-enriched membrane vesicles (100 µg protein ml−1, quantified using a BioRad Bradford protein assay) were added to start the reaction and incubated at 37°C for 1 h, then the reaction was stopped by the addition of 1% (w/v) SDS. Inorganic phosphate (Pi) release as a measure of enzyme hydrolytic activity was determined by colorimetric assay following addition of reductant and colour developer solutions as described by Ohnishi et al. , then quantified by absorbance measurement at 720 nm.
Proton transport measurements in the purified membrane vesicles were performed to assess the V-ATPase activity in each genotype. V-ATPase H+ transport was measured by the fluorescence quenching of acridine orange to determine the formation of inside-acid pH gradient across the tonoplast vesicle membrane. Ca2+/H+ and Mn2+/H+ exchange activity was determined in the membrane vesicles by measuring the Ca2+- and Mn2+-dependent dissipation of the V-ATPase-dependent pH gradient by acridine orange fluorescence quench. The fluorescence quench assay was performed essentially as described previously , . Membrane vesicles (50 µg protein) were added to a reaction buffer in a stirred cuvette containing 175 mM mannitol, 40 mM Tris-MES (pH 8.0), 50 mM KCl, 1 mM sodium azide, 0.1 mM sodium orthovanadate, and 5 µM acridine orange (Sigma), incubated at 25°C. The pH gradient was generated by energisation of the V-ATPase with the addition of 2 mM ATP and 2 mM MgSO4. The formation of the pH gradient was observed by monitoring the fluorescence quenching of acridine orange at excitation 495 nm and emission 540 nm using a Jasco FP750 fluorescence spectrometer. After a steady-state pH gradient was generated, 0.2 µM bafilomycin was added to inhibit V-ATPase activity then 200 µM of CaCl2 or MnCl2 were added and initial rate of fluorescence recovery measured. Analysis was conducted in duplicate or triplicate on each of three independently prepared membrane vesicles.
Unless otherwise stated, all data shown is representative of at least three repeat experiments. Differences between treatments were assessed using one-way ANOVA or two-way ANOVA. When significant differences were detected at a 95% level of confidence, the multi-range Tukey's post-hoc test was applied. All statistical tests were performed using SPSS version 16 for Windows.
Cation/H+ exchanger double knockouts display selective ion sensitivity phenotypes
A double mutant between the two closely related CAX genes CAX1 and CAX3 was previously shown to display significant growth impairment when grown on soil  or on basal nutrient solution . To examine the potential phenotypes of double mutants generated between two phylogenetically distinct CAX genes; CAX2 with either CAX1 or CAX3, the homozygous cax1-1, cax2-2 and cax3-1 knockout mutants which we previously isolated and characterised , ,  were crossed and cax1/cax2 and cax2/cax3 double mutants were selected in the F2 generation. Homozygous double mutant alleles were confirmed by PCR (data not shown), and lack of CAX1 and CAX2 expression (in cax1/cax2), and CAX2 and CAX3 expression (in cax2/cax3) was confirmed by real-time PCR (Figure 1). We previously found that knockout of CAX1 leads to significant induction of CAX3 expression . The cax2 and cax3 mutants showed a moderate induction of other CAX genes, with CAX1 and CAX3 (in cax2) and CAX1 (in cax3) induced slightly relative to wild type, while cax1/cax2 and cax2/cax3 displayed substantial induction of CAX3 and CAX1 expression, respectively (Figure 1). Induction of CAX2 was not significantly higher than wild type levels in cax1 and cax3 lines.
The cax1/cax2 and cax2/cax3 double mutants showed no significant deleterious morphological phenotypes when germinated and grown on soil and looked equivalent to the cax1, cax2 and cax3 single mutants rather than the cax1/cax3 mutant, which as shown previously , has a marked stunted phenotype on soil (Figure S1). However, on 0.5×MS agar medium, cax2/cax3 had reduced growth (Figure S2), which was significantly different to wild type as determined by fresh weight (Figure 2A). The cax1/cax2 and cax2/cax3 mutants were also tested on a range of ion stress conditions: 25 mM CaCl2, 10 µM CdCl2, 10 mM LiCl, 50 mM NaCl, 25 mM MgCl2, and 1.5 mM MnCl2. The fresh weight of seedlings under these conditions was measured and a two-way ANOVA of all stress treatment data combined (Table S1) found that cax1 and cax1/cax2 were the only genotypes to consistently differ significantly from wild type (P = 0.007 and P = 0.001, respectively). When the metal treatments were evaluated individually, only two treatments identified significant differences among the genotypes as determined by one-way ANOVA: Mg and Mn stress. Under our conditions, we could not see any significant difference to fresh weight of any of the knockout genotypes compared to wild type in response to any of the other metal treatments including Ca stress or Na stress. Both cax1 and cax1/cax2 showed tolerance to 25 mM MgCl2 stress and grew several-fold better than wild type and any other genotype (Figure 2B). Growth phenotypes were also detected in mutants sown on 1.5 mM MnCl2 conditions. The cax2 mutant showed increased sensitivity to Mn as demonstrated by reduced fresh weight compared to wild type, which was also seen in cax2/cax3, but when CAX2 was deleted alongside CAX1 (cax1/cax2 mutant) the plants were not sensitive to Mn (Figure 2C), indicating that the loss of CAX1 suppressed the cax2 Mn sensitivity phenotype. Although treatment with 50 mM NaCl did not yield significant alterations in fresh weight, it did impact on total chlorophyll (Chl a+b) content in some of the mutants. Increased salt sensitivity in terms of reduced chlorophyll content compared to treatment without NaCl was found for cax3 and cax2/cax3 (Figure 3). The effects of the other metal treatments to leaf chlorophyll content were also measured but there were no significant differences found between genotypes and between stress and non-stress conditions.
Fresh weight of Col-0 (wild type) and cax knockout mutant plants following germination and growth on solid 0.5×MS media (adjusted to pH 5.6) in the absence (A) or presence of 25 mM MgCl2 (B) or 1.5 mM MnCl2 (C). Bars indicate the mean±SE (n = 12–15) fresh weight measured in 21 d-old plants. ** (P<0.01) and * (P<0.05) denotes significant difference between CAX mutant lines and Col-0 control as determined by one-way ANOVA.
Total chlorophyll content was measured in leaf and shoot tissue of 21 d-old Col-0 (wild type) and cax knockout mutant plants following germination and growth on solid 0.5×MS media (adjusted to pH 5.6) in the absence or presence of 50 mM NaCl. The mean±SE (n = 4–6) chlorophyll content is shown. ** (P<0.01) denotes significant difference between control and NaCl treatments as determined by one-way ANOVA.
CAX gene mutation alters seed germination time
The CAX mutants were also examined for differences in germination. Approximately 100 seeds of each genotype were sown in a grid formation on 1% agar, stratified for 2 d in the dark at 4°C and then moved to an environmentally-controlled growth chamber. After a 9 h incubation period seeds were scored for radicle protrusion from the testa. The time-course of germination was divided into three phases for comparison: 0–9 h (‘early’), 9–21 h (‘intermediate’) and 21–37 h (‘late’), and the percentage of seeds germinating in each phase was calculated (Figure 4). Seeds from cax1, cax1/cax2 and cax2/cax3 germinated more slowly than wild type, with a greater percentage of seeds germinating in the late phase. The mean germination times of these three sets of mutant seeds ranged from 22.1 h to 25.3 h rather than 17.1 h to 19.2 h for the wild type, cax2 and cax3 seeds (Table 1). In order to further quantify the speed at which seeds germinate, the time required for 50% of viable seeds to germinate (T50) was calculated (Table 1). Wild type seeds germinated most quickly (T50 = 15.4 h), followed by single knockouts (T50 = ~18 h), with the double knockout seeds the slowest (T50 = ~21 h). Seeds were observed for a further 6 d and those found not to have germinated were considered non-viable. Maximum germination of the CAX mutant seeds ranged from 84.8% to 94.2%, with cax1/cax2 seeds having the poorest viability compared to wild type with maximal germination of 96.7% (Table 1). Only the cax2 knockout had a higher viability than wild type (97.1%).
Germination profile of CAX mutant seedlings over three time periods. Approximately 100 seeds from Col-0 (wild type) and cax knockout mutant plants were sterilized and sown on 1% agar plates. After a 2-d incubation period at 4°C plates were moved to an environmentally-controlled growth chamber at 22°C. Radicle emergence from the testa was taken as the indicator of germination. Stacked bars indicate the percentage of seeds germinating 0–9 hours, 9–21 hours and 21–37 hours after transfer to 22°C. All values are corrected for seed non-viability, determined by quantifying the absence of seed germination after 10 d.
The wild type and mutant seeds were also examined under a range of excess metal conditions: 25 mM CaCl2, 10 µM CdCl2, 10 mM LiCl, 50 mM NaCl, 25 mM MgCl2 and 1.5 mM MnCl2. A two-way ANOVA identified a significant influence of the cax1/cax2 genotype on seed viability, with these seeds being significantly less viable (P = 0.006) than wild type seeds and all other genotypes studied (Table S2). Establishment time, defined in this case as the time taken for the emergence of both cotyledons from the seed coat, was also measured. Mg, Mn and Li treatment had no significant effect on seedling establishment compared to no metal treatment, yet Ca treatment significantly delayed establishment in all seeds; however, no significant difference could be detected between any of the genotypes (Figure S3).
We previously found that cax1 and cax3 mutant seeds had reduced germination on media containing abscisic acid (ABA) when measured after 6 d . In order to investigate the influence of ABA on germination of the double knockout mutants, seeds were sown on 1% agar containing ABA and scored for germination after 24 h. All of the single and double knockout mutants were found to have a significantly lower germination rate than wild type seeds on 0.1 µM ABA (Figure 5). Furthermore, at this early time point, the sensitivity to ABA by the cax3 seeds particularly, and to a lesser extent the cax1/cax2 seeds, could be differentiated from the other knockout seeds, including cax1 and cax2.
Germination of CAX mutant seedlings in response to abscisic acid (ABA). The germination of seeds from Col-0 (wild type) and cax knockout mutant plants was quantified after 24 h on 0.1 µM ABA. Approximately 100 seeds of each line were sterilized and sown on 1% agar plates containing ABA. After a 2-d incubation period at 4°C plates were moved to an environmentally-controlled growth chamber at 22°C. Radicle emergence from the testa was taken as the indicator of germination. Bars indicate the mean±SE percentage of germination. ** (P<0.01) denotes significant difference between CAX mutant lines and Col-0 control as determined by one-way ANOVA.
CAX mutant seeds have altered seed mineral nutrient contents
Soil-grown wild type and mutant plants were subjected to ICP-AES element analysis to determine the mineral nutrient concentration in dried seeds (Figure S4) and leaves (Figure S5). Previously, we demonstrated minor nutrient concentration changes in the shoot tissue of cax1 plants but more significant changes in cax1/cax3 plants, particularly with respect to P, Mn and Zn . Likewise, under the growth conditions of this study we observed significant leaf nutrient concentration changes in cax1/cax3 compared to wild type: an increase in P and Zn, and a decrease in Na content (Figure S5). There was no change in leaf mineral concentration from the other CAX single and double knockout mutants compared to wild type. However, the seed mineral concentration profile was very different from that of the leaves (Figure S4). Due to the low number of cax1/cax3 seed that was available from this poor seed-yielding plant, cax1/cax3 seed elemental analysis was not performed, but seed from the other single and double mutants were examined. Ca2+, Mn2+, Na+ and Zn2+ have been demonstrated or indicated to be substrates of CAX1, CAX2 and CAX3 , , , . Ca concentration was significantly increased by 37% in cax1/cax2 seed compared to wild type (Figure 6A). cax2 and cax1/cax2 seed both had a significant increase in Mn concentration, by 32% and 40%, respectively, while Zn content was increased in cax2 and cax3 seed, by 19% and 14%, respectively. In all of the cax2, cax1/cax2, and cax2/cax3 seed, Fe, K and P concentration was higher than in wild type, while K and P concentration was increased in cax3 seed (Figure 6B).
The concentrations of known or putative substrates of CAX transporters: Ca, Mn, Na and Zn (A) and of metals not thought to be transported by CAX: Fe, K, Mg and P (B) are shown as % difference from Col-0 (wild type) seeds. Dry seeds (approximately 15 mg per sample) were obtained from plants grown on soil without additional metal supplementation. Elemental analysis was performed by ICP-AES measurement. Bars indicate the mean±SE of three replicates. * (P<0.05) denotes significant difference from Col-0 as determined by one-way ANOVA.
All CAX single and double knockouts show changes in cation/H+ exchange activity
In order to correlate the changes in CAX mutant metal stress response, seed germination and mineral nutrient concentration with vacuolar cation/H+ exchange activity, purified vacuolar-enriched membrane vesicles were isolated from wild type and knockout mutant seedlings. The isolated tonoplast-enriched vesicles were of high purity with low contamination from other membrane fractions, as determined by high inhibition of the nitrate- and bafilomycin-sensitive tonoplast V-ATPase and K+-dependent tonoplast H+-PPase activities (64–81% inhibition) and low inhibition of the vanadate-sensitive plasma membrane H+-ATPase and azide-sensitive mitochondrial H+-ATPase activities (11–12% inhibition) (Table S3). The purity and quality of membrane vesicles from each genotype were equivalent (Figure S6; data not shown).
H+ pump activity into the vesicles and cation/H+ exchange activity (Ca2+- or Mn2+-dependent H+ flux out of the vesicles) was determined by the fluorescence quenching and recovery of acridine orange. The initial rates of fluorescence quenching and recovery can be used to quantify the activity of the V-ATPase and cation/H+ exchange . The proton gradient across the tonoplast to drive the cation exchange is determined by the V-ATPase. Previously we have found that inhibition of CAX activity in cax1, cax2 and cax3 knockouts leads to a decrease in V-ATPase activity , , . This may influence the rate of H+-dependent cation exchange, therefore V-ATPase activity for all lines was analysed. V-ATPase-dependent H+ pumping into the wild type and knockout membrane vesicles was initiated by the addition of Mg2+-ATP, and then fluorescence quenching was observed until a steady-state pH gradient was obtained, which could be completely abolished by protonophore addition (data not shown). Consistent with previous studies, V-ATPase proton pumping activity (Figure S6) was reduced in the single cax1, cax2 and cax3 mutants compared to wild type, as determined by the initial rates of H+ transport over 1 min (Figure 7A), and were also reduced in the cax1/cax2 and cax2/cax3 mutants. However, there was no significant difference in V-ATPase activity between single and double cax knockout lines. Determination of V-ATPase activity by measurement of ATPase hydrolytic activity found equivalent differences between wild type and the CAX mutant plants (data not shown).
(A) Initial rates of V-ATPase H+ transport activity in purified vacuolar-enriched membrane vesicles from Col-0 (wild type) and cax knockout mutant plants determined from the rates of acridine orange fluorescence quenching during the first 60 sec following the addition of Mg-ATP, as shown in Figure S6. (B) and (C) Initial rates of ΔpH-dependent cation/H+ exchange activity in purified vacuolar-enriched membrane vesicles from Col-0 and cax knockout mutant plants determined from the rates of acridine orange fluorescence recovery during the first 60 sec following the establishment of a steady-state pH gradient and the addition of 200 µM CaCl2 (A) or MnCl2 (B), as shown in Figure S6. F indicates relative fluorescence intensity. Membrane vesicles were prepared from 2-week-old plants grown on solid 0.5×MS media and pre-treated with 50 mM CaCl2 and 1.5 mM MnCl2 14 h before harvest. The data represent means±SE from three experiments. ** (P<0.01) and * (P<0.05) denotes significant difference between CAX mutant lines and Col-0 control as determined by one-way ANOVA.
Despite the difference in V-ATPase activity between wild type and cax knockout mutants, there was no significant difference in final steady state levels of pH gradient between any of the lines. Significant quench recovery, indicating dissipation of the pH gradient, following the addition of 200 µM CaCl2 or MnCl2 was measured in the tonoplast-enriched vesicles purified from wild type plants, indicative of Ca2+/H+ and Mn2+/H+ exchange activity (Figure S6). Ca2+/H+ exchange activity as determined by the initial rate of Ca2+-dependent fluorescence recovery over 1 min was significantly reduced in cax1 and cax3, but not in cax2 (Figure 7B). Mn2+/H+ exchange activity was markedly reduced in cax2, but not at all in cax1 (Figure 7C). There was also a smaller reduction in Mn2+/H+ exchange activity in cax3. Ca2+/H+ exchange activity was significantly reduced in cax1/cax2 but not in cax2/cax3, while a large reduction in Mn2+/H+ exchange activity was equivalent in both double knockout lines.
Previous studies have indicated a number of physiological roles for CAX1, CAX2 and CAX3 in mature Arabidopsis plants . Although these genes are known to be expressed in seeds , , their function there remains unknown. Furthermore, previous work on the consequence of disrupting the function of CAX genes has been limited to single knockouts and one double knockout of two closely related genes (cax1/cax3) , , . This work therefore represents the first in-depth study into the significance of CAX function on seed physiology, and the physiological consequences of simultaneously knocking out CAX genes from different sub-families.
The data shown here suggest a hitherto unidentified role for the CAX transport pathway in seed Ca2+ homeostasis, and thus an influence on seed physiology. In particular cax1/cax2 seeds showed delayed germination time and a loss in seed viability (Figure 4; Table 1; Table S2), along with increased total Ca2+ concentration when compared to wild type and to all other mutants studied (Figure 6). This is especially interesting because analysis of CAX2 vacuolar transporter function suggests that the CAX2 phenotype does not directly influence the vacuolar Ca2+ transport of shoot tissue (Figure 7). It might be expected that a reduction in vacuolar Ca2+ sequestration through combined loss of CAX1 and CAX2 would lead to a reduction in Ca2+ concentration rather than the increase observed in the cax1/cax2 seed. Although there was a net reduction in Ca2+/H+ transport activity in the cax1/cax2 line in vegetative tissue, due to the large amount of tissue required it was not possible to measure transport activity in the cax1/cax2 seed and thus determine whether Ca2+/H+ exchange activity was higher than in vegetative tissue such as through up-regulation of other CAX transporters. We have previously found that there is a degree of compensation for loss of CAX activity and that other vacuolar Ca2+ transporters including Ca2+-ATPases are up-regulated in cax1 and cax1/cax3 knockout backgrounds , . We might therefore speculate that in the cax1/cax2 seed there is greater up-regulation and over-compensation by other Ca2+ transporters compared to in other tissues, resulting in more Ca2+ accumulation. Similarly, a potential up-regulation of other metal transporters may explain the increased metal concentration in the cax knockout seed.
Although significant alterations in seed Ca concentration were not consistently observed in all mutants exhibiting delayed germination, it is important to note that analysis of total seed content alone does not allow for the influence of sub-tissue (and indeed sub-cellular) partitioning of Ca2+ in seeds. A recent study into the distribution of Ca and other mineral nutrients within seeds of cax1, cax3 and cax1/cax3 knockout mutants found that only subtle changes in total seed Ca could be detected, but more dramatic changes were observed in the Ca partioning between the seed coat and embryo . Other previous studies have also indicated the importance of vacuolar mineral storage and transport in Arabidopsis seeds: in the developing seed, minerals are stored principally in the vacuoles of the embryo and the chalazal endosperm . Furthermore, when vacuolar release of these minerals is impaired, such as in nramp3 and nramp4 vacuolar metal transporter knockout mutants, delays are seen in germination and early development . Although there was no single metal change that correlated with a delay in germination within the data set in this study, it is possible that the increased total metal burden within the seeds had effects similar to external metal toxicity on the seeds and thus inhibited germination. However, we found that increased levels of external Ca in particular led to a delay in seedling establishment in all plants, although there was no difference between wild type and CAX mutant lines (Figure S3). Excess Ca also inhibits seedling development at the earlier germination stage and when Ca homeostasis is compromised such as in cax1, cax3 and cax1/cax3 backgrounds, germination in the presence of external Ca is further delayed . Seed germination is a complex process depending on the combined functioning of many different processes; however, it has been suggested that a number of the reactions involved, such as ABA-mediated dormancy, are governed in part by cytosolic Ca2+ flux –. Germination was delayed in all CAX mutant lines (Table 1) and ABA-dependent germination inhibition was greater in all CAX lines compared to wild type (Figure 5). It is therefore tempting to speculate that perturbed CAX function in mutant seeds may lead to disruption in Ca2+ signalling dynamics through inhibited vacuolar Ca2+ uptake, which may in turn delay germination. Previous studies have shown that mutant Arabidopsis seeds lacking the vacuolar Ca2+ release channel TPC1 are insensitive to ABA-induced repression of germination and thus germinate more rapidly than wild type seeds .
Although originally identified as Ca2+ transporters, CAX1, CAX2 and CAX3 are now known to also be able to transport other ions including Mn2+ and Cd2+ , , . Their specificities do not appear to be a consequence of the phylogenetic groupings, with CAX1 and CAX3 being members of the Type 1-A subfamily and CAX2 being a member of the Type 1-B subfamily . The significance of these groupings is unknown, however, while knockouts of single CAX genes show very subtle phenotypes, plants lacking two CAX genes (CAX1 and CAX3) were previously shown to exhibit a dramatic stunted phenotype, which is consistent with the equivalent and partially overlapping Ca2+ transport function of both transporters . Although CAX2 is up-regulated in the cax1/cax3 plant, it is clearly unable to compensate , . Here we show, in contrast, that knocking out CAX1 and CAX2 simultaneously does not result in obvious deleterious phenotypes on soil (Figure S1). There is however, a small but significant decrease in fresh weight in cax2/cax3 mutants grown under controlled conditions on solid MS agar medium (Figure 2 and S2), suggesting slight perturbations to seedling growth.
Metals including Mg and Mn did not significantly affect seedling establishment (Figure S3) but did have an effect later in development of the plants. When grown in the presence of high external Mg, cax1 and cax1/cax2 seedlings were significantly more tolerant than wild type and all other mutants studied (Figure 2). Tolerance of cax1 mutants to Mg has been previously reported , . However, it is interesting to note that in this study cax1/cax2 was phenotypically similar to cax1 and not cax2 (Figure 2B). This, more surprisingly, also appears to be the case when mutants were grown in the presence of high external Mn. Here cax2 seedlings were significantly smaller than wild type seedlings, potentially due to vacuolar Mn2+ sequestration in the wild type and thus the Mn tolerance role of CAX2 , . However, cax1/cax2 seedlings are more phenotypically equivalent to cax1 than cax2 on Mn medium, and do not show any signs of Mn sensitivity, despite a reduction in Mn2+/H+ exchange activity (Figure 7). Indeed mutants lacking CAX1 have previously been shown to display a degree of tolerance to excess Mn . It appears therefore that the status of the CAX1 gene dominates the physiology of the seedling in response to Mn stress. Furthermore, a statistical analysis of the impact of CAX mutation on the response to metal stress established that only cax1 and cax1/cax2 are consistently significantly different to wild type; indeed cax1/cax2 was significantly different from all other genotypes studied except cax1 (Table S1).
Other metal stresses did not affect the fresh weight of the single and double CAX mutant plants any differently than wild type. This included 25 mM Ca stress, which we previously found caused a slight increased reduction in growth of cax3 seedlings compared to wild type . However, under the experimental conditions of this study we did not observe any significant difference in fresh weight between wild type and mutants including cax3 and cax2/cax3. Furthermore, no differences in plant fresh weight were found with the wild type and CAX mutant lines in response to NaCl stress but knockouts of cax3 and cax2/cax3 were found to contain significantly less chlorophyll when grown on media supplemented with NaCl (Figure 3). This corresponds with the genotypes with elevated levels of CAX1 transcript (Figure 1), and we have also previously found that 35S-CAX1 overexpression plants are more sensitive to NaCl . Several studies implicate CAX proteins in Na+ transport , , , and CAX1 is thought to be activated by SOS2 (CIPK24), the protein kinase important for salt tolerance and ion homeostasis , . Furthermore, NaCl stress can stimulate Ca2+ influx in the cytoplasm, while Na+ transport is in part regulated by a signalling cascade beginning with Ca2+ sensors such as CBL10 , . Although it is not known to what extent alterations in vacuolar Ca2+ transporters are responsible for altered NaCl sensitivity it is possible that increased levels of CAX1, which lead to a reduction in cytosolic Ca2+ due to elevated vacuolar sequestration , perturb the normal cellular response to high NaCl.
In conclusion, the data presented here identify evidence of a complex system of cross-talk among members of the cation/H+ exchanger family and compensatory mechanisms accounting for the subtleties in phenotypes associated with loss of function of one family member with regard to the normal physiology of the plant. However, individual members of the family, notably CAX1, appear to have a more pronounced role in determining the physiology of the plant under conditions of metal stress. Additionally, evidence presented here indicates an important role for CAX proteins in seed germination and development, which may be linked particularly to maintenance of Ca homeostasis. Further work is required to elucidate the precise contribution of the family members to these processes and their potential applications.
Morphological phenotype comparisons of the cax1/cax2 and cax2/cax3 double knockout mutant lines with the cax1/cax3 line. cax single and double knockout lines were grown on soil alongside Col-0 (wild type). Representative plants from each line are shown after 4 weeks growth under continuous light at 22°C. Only the cax1/cax3 plants exhibit the stunted, leaf tip necrosis phenotype.
Growth of CAX mutant plants on 0.5×MS agar plates. Growth of Col-0 (wild type) and cax knockout mutant lines on solid 0.5×MS media (adjusted to pH 5.6). Representative plants from each line are shown after 21 days growth.
Mean establishment time of CAX mutant seedlings in response to metal stress. Seeds from Col-0 (wild type) and cax knockout plants (approximately 15 per line) were sterilized and sown on media with or without metal supplements (1.5 mM MnCl2, 10 mM LiCl, 25 mM MgCl2, or 25 mM CaCl2). Seeds were stratified for 2 d at 4°C and then incubated under a 22°C 16 h light/8 h dark cycle. Seeds were observed every 24 h under a dissection microscope and the mean time for the seedlings to establish (the time for both cotyledons to clearly emerge from the seed coat) was determined for each line, using the equation Σ(NtT)/Σn where Nt is the number of seeds established at each time point, T is the time point, and n is the total number of seeds. Bars indicate the mean±SE of 4 replicate experiments. ** (P<0.01) denotes significant difference of Ca treatment from control (non-metal stressed) treatment, as determined by one-way ANOVA.
Nutrient concentration of dry seeds from CAX mutant plants. Dry seeds (approximately 15 mg per sample) were obtained from Col-0 (wild type) and cax knockout plants grown on soil without additional metal supplementation. Quantification of Ca (A), Fe (B), K (C), Mg (D), Mn (E), Na (F), P (G) and Zn (H) was performed by ICP-AES. Bars indicate the mean±SE of three replicates. ** (P<0.01) and * (P<0.05) denotes significant difference from Col-0 as determined by one-way ANOVA.
Nutrient concentration of leaves from CAX mutant plants. Leaves (approximately 15 mg per sample) were obtained from 4-week-old Col-0 (wild type) and cax knockout plants grown on soil without additional metal supplementation. Quantification of Ca (A), Fe (B), K (C), Mg (D), Mn (E), Na (F), P (G) and Zn (H) was performed by ICP-AES. Bars indicate the mean±SE of three replicates. ** (P<0.01) and * (P<0.05) denotes significant difference from Col-0 as determined by one-way ANOVA.
V-ATPase-dependent quenching and cation-dependent recovery of acridine orange fluorescence in vacuolar-enriched membrane vesicles from CAX mutant plants. Proton transport is shown in Col-0 (wild type) (A), cax1 (B), cax2 (C), cax3 (D), cax1/cax2 (E) and cax2/cax3 (F) lines. Membrane vesicles were prepared from 2-week-old plants grown on solid 0.5×MS media and pre-treated with 50 mM CaCl2 and 1.5 mM MnCl2 14 h before harvest. Proton pumping and generation of a pH gradient initiated by the addition of Mg-ATP at the time shown (arrow) was measured by the quenching of acridine orange fluorescence. When the steady-state pH gradient was obtained, 0.2 µM bafilomycin was added to inhibit V-ATPase activity. Immediately after this, Ca2+- and Mn2+-dependent dissipation of the pH gradient was measured by the recovery of acridine orange fluorescence following the addition of 200 µM CaCl2 (red line) or 200 µM MnCl2 (blue line) at the time shown (arrow). F indicates relative fluorescence intensity. Representative traces are shown from three experiments.
Univariate statistical analysis of the fresh weight of CAX mutant plants in response to metal stress. The fresh weight of Col-0 (wild type) and cax knockout seedlings was determined 21 d after sowing on 0.5×MS (pH 5.6) medium supplemented with 25 mM CaCl2, 10 µM CdCl2, 10 mM LiCl, 50 mM NaCl, 25 mM MgCl2, 1.5 mM MnCl2, or no supplements, then incubation at 22°C under a 16 h light/8 h dark cycle. A two-way ANOVA with Tukey post-hoc test on the variance in fresh weight of mutant seedlings in response to metal stress identified the following significant differences (* P<0.05; ** P<0.01; *** P<0.001); n = 889.
Univariate statistical analysis of the viability of CAX mutant seeds in response to metal stress. The viability of Col-0 (wild type) and cax knockout seeds was determined 10 d after sowing on 1% agar medium alone or supplemented with 25 mM CaCl2, 10 µM CdCl2, 10 mM LiCl, 50 mM NaCl, 25 mM MgCl2, or 1.5 mM MnCl2. Following sowing, seeds were stratified for 2 d at 4°C in the dark then incubated at 22°C under a 16 h light/8 h dark cycle. Any seeds not germinated after 10 d were considered non-viable. A two-way ANOVA with Tukey post-hoc test on the viability of seeds of the various mutants in response to metal stress identified the following significant differences (* P<0.05); n = 105.
The effects of inhibitors on H+ pump hydrolytic activity in vacuolar-enriched membrane vesicles. Membrane vesicles were prepared from 2-week-old Col-0 (wild type) plants. ATPase activity (µmol Pi mg−1 protein h−1) at pH 8.0 (unless indicated) was measured in the presence of 2 mM ATP, 2 mM MgSO4 and 50 mM KCl. Pyrophosphatase (PPase) activity (µmol Pi mg−1 protein h−1) at pH 8.0 was measured in the presence of 0.1 mM pyrophosphate, 5 mM MgSO4 and 50 mM KCl. All reactions were performed over a 1 h incubation period at 37°C. Inhibitors of the plasma membrane H+-ATPase (vanadate), tonoplast H+-ATPase (nitrate and bafilomycin), mitochondrial ATPase (azide) and tonoplast K+-dependent H+-PPase (- KCl) were used. Mean activity (±SE) from three replicates is shown. n.d. – not determined.
We are grateful to Paul Lythgoe (Manchester Analytical Geochemical Unit, School of Earth, Atmospheric and Environmental Sciences, University of Manchester) for performing ICP-AES analysis.
Conceived and designed the experiments: JMC JKP. Performed the experiments: JMC REW NHC JKP. Analyzed the data: JMC REW NHC JKP. Contributed reagents/materials/analysis tools: NHC JKP. Wrote the paper: JMC REW NHC JKP.
- 1. Colangelo EP, Guerinot ML (2006) Put the metal to the petal: metal uptake and transport throughout plants. Curr Opin Plant Biol 9: 322–330. doi: 10.1016/j.pbi.2006.03.015
- 2. Puig S, Penarrubia L (2009) Placing metal micronutrients in context: transport and distribution in plants. Curr Opin Plant Biol 12: 299–306. doi: 10.1016/j.pbi.2009.04.008
- 3. Karley AJ, White PJ (2009) Moving cationic minerals to edible tissues: potassium, magnesium, calcium. Curr Opin Plant Biol 12: 291–298. doi: 10.1016/j.pbi.2009.04.013
- 4. Baxter I (2009) Ionomics: studying the social network of mineral nutrients. Curr Opin Plant Biol 12: 381–386. doi: 10.1016/j.pbi.2009.05.002
- 5. Manohar M, Shigaki T, Hirschi KD (2011) Plant cation/H+ exchangers (CAXs): biological functions and genetic manipulations. Plant Biol 13: 561–569. doi: 10.1111/j.1438-8677.2011.00466.x
- 6. Peiter E (2011) The plant vacuole: Emitter and receiver of calcium signals. Cell Calcium 50: 120–128. doi: 10.1016/j.ceca.2011.02.002
- 7. Martinoia E, Maeshima M, Neuhaus HE (2007) Vacuolar transporters and their essential role in plant metabolism. J Exp Bot 58: 83–102. doi: 10.1093/jxb/erl183
- 8. Lanquar V, Ramos MS, Lelievre F, Barbier-Brygoo H, Krieger-Liszkay A, et al. (2010) Export of vacuolar manganese by AtNRAMP3 and AtNRAMP4 is required for optimal photosynthesis and growth under manganese deficiency. Plant Physiol 152: 1986–1999. doi: 10.1104/pp.109.150946
- 9. Shigaki T, Rees I, Nakhleh L, Hirschi KD (2006) Identification of three distinct phylogenetic groups of CAX cation/proton antiporters. J Mol Evol 63: 815–825. doi: 10.1007/s00239-006-0048-4
- 10. Pittman JK (2011) Vacuolar Ca2+ uptake. Cell Calcium 50: 139–146. doi: 10.1016/j.ceca.2011.01.004
- 11. Cheng NH, Pittman JK, Shigaki T, Lachmansingh J, LeClere S, et al. (2005) Functional association of Arabidopsis CAX1 and CAX3 is required for normal growth and ion homeostasis. Plant Physiol 138: 2048–2060. doi: 10.1104/pp.105.061218
- 12. Conn SJ, Gilliham M, Athman A, Schreiber AW, Baumann U, et al. (2011) Cell-specific vacuolar calcium storage mediated by CAX1 regulates apoplastic calcium concentration, gas exchange, and plant productivity in Arabidopsis. Plant Cell 23: 240–257. doi: 10.1105/tpc.109.072769
- 13. McAinsh MR, Pittman JK (2009) Shaping the calcium signature. New Phytol 181: 275–294. doi: 10.1111/j.1469-8137.2008.02682.x
- 14. Dodd AN, Kudla J, Sanders D (2010) The language of calcium signaling. Annu Rev Plant Biol 61: 593–620. doi: 10.1146/annurev-arplant-070109-104628
- 15. Cheng NH, Pittman JK, Barkla BJ, Shigaki T, Hirschi KD (2003) The Arabidopsis cax1 mutant exhibits impaired ion homeostasis, development, and hormonal responses and reveals interplay among vacuolar transporters. Plant Cell 15: 347–364. doi: 10.1105/tpc.007385
- 16. Catalá R, Santos E, Alonso JM, Ecker JR, Martínez-Zapater JM, et al. (2003) Mutations in the Ca2+/H+ transporter CAX1 increase CBF/DREB1 expression and the cold-acclimation response in Arabidopsis. Plant Cell 15: 2940–2951. doi: 10.1105/tpc.015248
- 17. Zhao J, Barkla BJ, Marshall J, Pittman JK, Hirschi KD (2008) The Arabidopsis cax3 mutants display altered salt tolerance, pH sensitivity and reduced plasma membrane H+-ATPase activity. Planta 227: 659–669. doi: 10.1007/s00425-007-0648-2
- 18. Hirschi KD, Korenkov VD, Wilganowski NL, Wagner GJ (2000) Expression of Arabidopsis CAX2 in tobacco. Altered metal accumulation and increased manganese tolerance. Plant Physiol 124: 125–133. doi: 10.1104/pp.124.1.125
- 19. Shigaki T, Pittman JK, Hirschi KD (2003) Manganese specificity determinants in the Arabidopsis metal/H+ antiporter CAX2. J Biol Chem 278: 6610–6617. doi: 10.1074/jbc.m209952200
- 20. Edmond C, Shigaki T, Ewert S, Nelson M, Connorton J, et al. (2009) Comparative analysis of CAX2-like cation transporters indicates functional and regulatory diversity. Biochem J 418: 145–154. doi: 10.1042/bj20081814
- 21. Koren'kov V, Park S, Cheng NH, Sreevidya C, Lachmansingh J, et al. (2007) Enhanced Cd2+-selective root-tonoplast-transport in tobaccos expressing Arabidopsis cation exchangers. Planta 225: 403–411. doi: 10.1007/s00425-006-0352-7
- 22. Mei H, Cheng NH, Zhao J, Park P, Escareno RA, et al. (2009) Root development under metal stress in Arabidopsis thaliana requires the H+/cation antiporter CAX4. New Phytol 183: 95–105. doi: 10.1111/j.1469-8137.2009.02831.x
- 23. Manohar M, Shigaki T, Mei H, Park S, Marshall J, et al. (2011) Characterization of Arabidopsis Ca2+/H+ exchanger CAX3. Biochemistry 50: 6189–6195. doi: 10.1021/bi2003839
- 24. Kamiya T, Akahori T, Maeshima M (2005) Expression profile of the genes for rice cation/H+ exchanger family and functional analysis in yeast. Plant Cell Physiol 46: 1735–1740. doi: 10.1093/pcp/pci173
- 25. Pittman JK, Shigaki T, Marshall JL, Morris JL, Cheng NH, et al. (2004) Functional and regulatory analysis of the Arabidopsis thaliana CAX2 cation transporter. Plant Mol Biol 56: 959–971. doi: 10.1007/s11103-004-6446-3
- 26. Zhao J, Shigaki T, Mei H, Guo YQ, Cheng NH, et al. (2009) Interaction between Arabidopsis Ca2+/H+ exchangers CAX1 and CAX3. J Biol Chem 284: 4605–4615. doi: 10.1074/jbc.m804462200
- 27. Shigaki T, Mei H, Marshall J, Li X, Manohar M, et al. (2010) The expression of the open reading frame of Arabidopsis CAX1, but not its cDNA, confers metal tolerance in yeast. Plant Biol 12: 935–939. doi: 10.1111/j.1438-8677.2010.00368.x
- 28. Bradshaw HD (2005) Mutations in CAX1 produce phenotypes characteristic of plants tolerant to serpentine soils. New Phytol 167: 81–88. doi: 10.1111/j.1469-8137.2005.01408.x
- 29. Broadley MR, Bowen HC, Cotterill HL, Hammond JP, Meacham MC, et al. (2004) Phylogenetic variation in the shoot mineral concentration of angiosperms. J Exp Bot 55: 321–336. doi: 10.1093/jxb/erh002
- 30. Liu T-Y, Aung K, Tseng C-Y, Chang T-Y, Chen Y-S, et al. (2011) Vacuolar Ca2+/H+ transport activity is required for systemic phosphate homeostasis involving shoot-to-root signaling in Arabidopsis. Plant Physiol 156: 1176–1189. doi: 10.1104/pp.111.175257
- 31. Emery L, Whelan S, Hirschi KD, Pittman JK (2012) Protein phylogenetic analysis of Ca2+/cation antiporters and insights into their evolution in plants. Front Plant Sci 3: 1. doi: 10.3389/fpls.2012.00001
- 32. Winter D, Vinegar B, Nahal H, Ammar R, Wilson GV, et al. (2007) An “electronic fluorescent pictograph” browser for exploring and analyzing large-scale biological data sets. PLoS ONE 2: e718. doi: 10.1371/journal.pone.0000718
- 33. Punshon T, Hirschi K, Yang J, Lanzirotti A, Lai B, et al. (2012) The role of CAX1 and CAX3 in elemental distribution and abundance in Arabidopsis seed. Plant Physiol 158: 352–362. doi: 10.1104/pp.111.184812
- 34. Porra RJ, Thompson WA, Kriedemann PE (1989) Determination of accurate extinction coefficients and simultaneous-equations for assaying chlorophyll-a and chlorophyll-b extracted with 4 different solvents - verification of the concentration of chlorophyll standards by atomic-absorption spectroscopy. Biochim Biophys Acta 975: 384–394. doi: 10.1016/s0005-2728(89)80347-0
- 35. Bewley JD, Black M (1994) Seeds: Physiology of Development and Germination. New York: Plenum Press.
- 36. Ruijter JM, Ramakers C, Hoogaars WMH, Karlen Y, Bakker O, et al. (2009) Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Res 37: e45. doi: 10.1093/nar/gkp045
- 37. Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29: e45. doi: 10.1093/nar/29.9.e45
- 38. Barkla BJ, Zingarelli L, Blumwald E, Smith JAC (1995) Tonoplast Na+/H+ antiport activity and its energization by the vacuolar H+-ATPase in the halophytic plant Mesembryanthemum crystallinum L. Plant Physiol. 109: 549–556.
- 39. Williams LE, Schueler SB, Briskin DP (1990) Further characterization of the red beet plasma-membrane Ca2+-ATPase using GTP as an alternative substrate. Plant Physiol 92: 747–754. doi: 10.1104/pp.92.3.747
- 40. Ohnishi T, Gall RS, Mayer ML (1975) Improved assay of inorganic-phosphate in presence of extralabile phosphate compounds - application to atpase assay in presence of phosphocreatine. Anal Biochem 69: 261–267. doi: 10.1016/0003-2697(75)90585-0
- 41. Delhaize E, Gruber BD, Pittman JK, White RG, Leung H, et al. (2007) A role for the AtMTP11 gene of Arabidopsis in manganese transport and tolerance. Plant J 51: 198–210. doi: 10.1111/j.1365-313x.2007.03138.x
- 42. Bennett AB, Spanswick RM (1983) Optical measurements of ΔpH and Δψ in corn root membrane vesicles: kinetic analysis of Cl− effects on a proton-translocating ATPase. J Membr Biol 71: 95–107. doi: 10.1007/bf01870678
- 43. Otegui MS, Capp R, Staehelin LA (2002) Developing seeds of Arabidopsis store different minerals in two types of vacuoles and in the endoplasmic reticulum. Plant Cell 14: 1311–1327. doi: 10.1105/tpc.010486
- 44. Lanquar V, Lelievre F, Bolte S, Hames C, Alcon C, et al. (2005) Mobilization of vacuolar iron by AtNRAMP3 and AtNRAMP4 is essential for seed germination on low iron. EMBO J 24: 4041–4051. doi: 10.1038/sj.emboj.7600864
- 45. Guo Y, Xiong LM, Song CP, Gong DM, Halfter U, et al. (2002) A calcium sensor and its interacting protein kinase are global regulators of abscisic acid signaling in Arabidopsis. Dev Cell 3: 233–244. doi: 10.1016/s1534-5807(02)00229-0
- 46. Leung J, Giraudat J (1998) Abscisic acid signal transduction. Annu Rev Plant Physiol Plant Mol Biol 49: 199–222. doi: 10.1146/annurev.arplant.49.1.199
- 47. Lovegrove A, Hooley R (2000) Gibberellin and abscisic acid signalling in aleurone. Trends Plant Sci 5: 102–110. doi: 10.1016/s1360-1385(00)01571-5
- 48. Peiter E, Maathuis FJM, Mills LN, Knight H, Pelloux M, et al. (2005) The vacuolar Ca2+-activated channel TPC1 regulates germination and stomatal movement. Nature 434: 404–408. doi: 10.1038/nature03381
- 49. Pittman JK (2005) Managing the manganese: molecular mechanisms of manganese transport and homeostasis. New Phytol 167: 733–742. doi: 10.1111/j.1469-8137.2005.01453.x
- 50. Cheng NH, Pittman JK, Zhu JK, Hirschi KD (2004) The protein kinase SOS2 activates the Arabidopsis H+/Ca2+ antiporter CAX1 to integrate calcium transport and salt tolerance. J Biol Chem 279: 2922–2926. doi: 10.1074/jbc.m309084200
- 51. Zhao J, Connorton JM, Guo YQ, Li XK, Shigaki T, et al. (2009) Functional studies of split Arabidopsis Ca2+/H+ exchangers. J Biol Chem 284: 34075–34083. doi: 10.1074/jbc.m109.070235
- 52. Zhu J-K, Liu J, Xiong L (1998) Genetic Analysis of salt tolerance in Arabidopsis: Evidence for a critical role of potassium nutrition. Plant Cell 10: 1181–1192. doi: 10.1105/tpc.10.7.1181
- 53. Serrano R, Rodriguez-Navarro A (2001) Ion homeostasis during salt stress in plants. Curr Opin Cell Biol 13: 399–404. doi: 10.1016/s0955-0674(00)00227-1
- 54. Kim BG, Waadt R, Cheong YH, Pandey GK, Dominguez-Solis JR, et al. (2007) The calcium sensor CBL10 mediates salt tolerance by regulating ion homeostasis in Arabidopsis. Plant J 52: 473–484. doi: 10.1111/j.1365-313x.2007.03249.x
- 55. Hirschi KD (1999) Expression of Arabidopsis CAX1 in tobacco: Altered calcium homeostasis and increased stress sensitivity. Plant Cell 11: 2113–2122. doi: 10.1105/tpc.11.11.2113