TY - JOUR
AU - Sze, Heven
AB - Abstract Ca2+ is required for protein processing, sorting, and secretion in eukaryotic cells, although the particular roles of the transporters involved in the secretory system of plants are obscure. One endomembrane-type Ca-ATPase from Arabidopsis (Arabidopsis thaliana), AtECA3, diverges from AtECA1, AtECA2, and AtECA4 in protein sequence; yet, AtECA3 appears similar in transport activity to the endoplasmic reticulum (ER)-bound AtECA1. Expression of AtECA3 in a yeast (Saccharomyces cerevisiae) mutant defective in its endogenous Ca2+ pumps conferred the ability to grow on Ca2+-depleted medium and tolerance to toxic levels of Mn2+. A green fluorescent protein-tagged AtECA3 was functionally competent and localized to intracellular membranes of yeast, suggesting that Ca2+ and Mn2+ loading into internal compartment(s) enhanced yeast proliferation. In mesophyll protoplasts, AtECA3-green fluorescent protein associated with a subpopulation of endosome/prevacuolar compartments based on partial colocalization with the Ara7 marker. Interestingly, three independent eca3 T-DNA disruption mutants showed severe reduction in root growth normally stimulated by 3 mm Ca2+, indicating that AtECA3 function cannot be replaced by an ER-associated AtECA1. Furthermore, root growth of mutants is sensitive to 50 μ m Mn2+, indicating that AtECA3 is also important for the detoxification of excess Mn2+. Curiously, Ateca3 mutant roots produced 65% more apoplastic protein than wild-type roots, as monitored by peroxidase activity, suggesting that the secretory process was altered. Together, these results demonstrate that the role of AtECA3 is distinct from that of the more abundant ER AtECA1. AtECA3 supports Ca2+-stimulated root growth and the detoxification of high Mn2+, possibly through activities mediated by post-Golgi compartments that coordinate membrane traffic and sorting of materials to the vacuole and the cell wall. The dynamic endomembrane system is emerging as a central coordinator of plant growth, development, and adaptation to abiotic and biotic stress. Cell biologists have long studied the biogenesis and roles of organelles, like the vacuoles and the Golgi, and the cellular and biochemical bases of protein sorting, membrane trafficking, and secretion (Battey and Blackbourn, 1993; Battey et al., 1999). For instance, noncellulosic cell wall precursors are synthesized in the Golgi and delivered in secretory vesicles to the outside of the cell (Carpita and McCann, 2000; Nebenfuhr and Staehelin, 2001). Newly synthesized secreted and membrane proteins at the endoplasmic reticulum (ER) are sorted to their destinations via vesicle or tubular trafficking, although the specific players and mechanisms are for the most part unclear. Recent advances were stimulated by numerous new findings emerging from molecular genetic investigations and proteins predicted by the completed genome of Arabidopsis (Arabidopsis thaliana). For example, the dynamics of PIN auxin transporters are revealing the intriguing complexity of relationships between endosomal trafficking, signaling, and development (Geldner, 2004). Endosomal trafficking refers to the movement of vesicles formed from endocytosis to remove functional plasma membrane proteins or to retrieve proteins for recycling purposes. The biosynthetic and endosomal vesicle traffic merge inside cells, although the molecular bases that ensure the smooth operation of multiple trafficking patterns are poorly understood. Ca2+ has long been recognized as an important ion for plant growth and the secretory process (Steer, 1988; Marschner, 1995; Brandizzi and Hawes, 2004). Ca2+ is required for root growth, although most of the Ca2+ in the plant body is associated with pectins outside the cell. Whether wall-associated Ca2+ is supplied from intracellular or external sources is debatable. Inside plant cells, membrane compartments forming the secretory pathway, such as the ER and Golgi apparatus, are filled with Ca2+ (Dauwalder et al., 1985; Sakai-Wada and Yagi, 1993), as in animal cells (Rizzuto and Pozzan, 2006). Furthermore, an elevation of cytosolic free Ca2+ ([Ca2+]cyt) stimulates exocytosis (Steer, 1988; Homann and Tester, 1997). In plants, polarized tip growth of pollen tube or root hair is thought to be the result of polarized secretion. Such tip growth is often accompanied by a steep gradient in [Ca2+]cyt at the tip as well as by Ca2+ oscillations (Hepler et al., 2001). However, little is known about the cellular and biochemical bases of the Ca2+ dynamics and their effects on plant growth. Ca2+ transporters, including channels, pumps, and H+/Ca2+ exchangers, identified from the Arabidopsis and rice (Oryza sativa) genomes are proposed to work together to regulate diverse Ca2+ transients and oscillations in a spatiotemporal manner required for growth and development (Sanders et al., 1999; Sze et al., 2000). However, only a few of the 14 Arabidopsis pumps have been functionally characterized at the molecular level. Two Ca2+ pumps, AtECA1 and ACA2 (for autoinhibited Ca2+-ATPase2), are localized to the ER of vegetative tissues and are thought to supply Ca2+ for functions in the ER lumen (Liang et al., 1997; Harper et al., 1998). Two Arabidopsis ACA proteins are localized to the plasma membrane (ACA8 and ACA9), where extrusion of Ca2+ would decrease cytosolic Ca2+ concentration in vegetative tissues (Bonza et al., 2000) or in pollen tubes (Schiott et al., 2004). Another Ca2+ pump, ACA4, localized to the vacuole or perhaps the prevacuolar compartment (PVC) could fill vacuolar stores and may have a role in stress tolerance (Geisler et al., 2000). Intriguingly, there is no secretory pathway-like Ca2+ pump (SPCA) gene in plants to date, based on phylogenetic analyses of Ca2+ pumps from cyanobacteria, fungi, and animals (Baxter et al., 2003; Li, 2006). SPCA Ca2+ pumps like the yeast (Saccharomyces cerevisiae) PMR1 or human SPCA1 are localized to the Golgi and participate in protein modification, sorting, and secretion (Durr et al., 1998; Wuytack et al., 2003). Here, we show that AtECA3 is a distinct Ca2+/Mn2+ pump critical for Ca2+-enhanced root growth and for tolerance to toxic levels of Mn2+. Unlike the ER-bound AtECA1, it is localized to post-Golgi compartments. Furthermore, mutants showed enhanced secretion of peroxidases, suggesting that an adequate supply of Ca2+ and Mn2+ in post-Golgi compartments is critical for regulated protein sorting. Thus, a novel Ca2+/Mn2+ pump promotes root growth, possibly through the activities of endosomes involved in sorting, membrane trafficking, and secretion. Our findings differ in several respects from a recent report (Mills et al., 2008) and show that AtECA3 has roles in plants beyond Mn2+ nutrition. RESULTS AtECA3 Shares High Sequence Identity with Animal Sarcoplasmic/ER Ca2+-ATPase Several ECAs from Arabidopsis, rice, and tomato (Solanum lycopersicum) clustered on a phylogenetic tree with mammalian sarcoplasmic/ER Ca2+-ATPase (SERCA; Fig. 1A Figure 1. Open in new tabDownload slide AtECA3 shares high similarity with animal SERCA. A, Phylogenetic relationships of type 2A Ca2+-ATPases from plant, cyanobacterium, yeast, and animal. SPCA, SERCA, and ECA refer to secretory pathway, sarcoplasmic reticulum/ER, and endomembrane Ca-ATPase, respectively. Protein names shown are preceded by genus and species initials. Arabidopsis (At) and rice (Os) ECA proteins are identified by their accession numbers in parentheses: AtECA1 (AAC68819; At1g07810), AtECA2 (CAA10659; At4g00900), AtECA3 (AAT68271; At1g10130), AtECA4 (AAD29957; At1g07670), OsECA1 (AAN64492; Os03g17310), OsECA2 (BAA90510; Os05g02940), and OsECA3 (ABF98693; Os03g52090). Other Ca2+ pumps aligned are Synechococcus elongatus SyoPacL (BAA03906); Saccharomyces cerevisiae ScPmr1 (P13586) and ScPmc1 (P38929); tomato LCA1 (Q42883); human (Hs) SERCA1 (O14983), SERCA2 (P16615), SERCA3 (Q93084), SPCA1 (AAH28139), and SPCA2 (AAV54193); Drosophila melanogaster (Dm) Ca-P60A (P22700) and SPoCk (AAN12202); and Oryctolagus cuniculus (rabbit) OcSERCA1a (PDB_ID 1SU4_A). The tree was aligned by T-Coffee. Values shown indicate the number of times (percent) that each branch topology was found in 1,000 replicates of the performed bootstrap analysis using PAUP* 4.0b10. B, Partial alignment of plant and other Ca2+-ATPases containing thapsigargin-interacting regions. Residue numbers correspond to rabbit SERCA1a or HsSERCA1. Black triangles indicate amino acid residues in direct contact with thapsigargin of rabbit SERCA1a (1SU4_A; Toyoshima and Nomura, 2002). Identical residues are shaded in black, while similar residues are boxed. TM3, TM5, and TM7 correspond to transmembrane regions of HsSERCA1. This alignment was generated in ESPript 2.2 (Gouet et al., 1999) using a T-Coffee-generated alignment. α-Helix, β-sheet, and turn are indicated as helix, black arrow, and T, respectively. The full alignment is shown in Supplemental Figure S1. Figure 1. Open in new tabDownload slide AtECA3 shares high similarity with animal SERCA. A, Phylogenetic relationships of type 2A Ca2+-ATPases from plant, cyanobacterium, yeast, and animal. SPCA, SERCA, and ECA refer to secretory pathway, sarcoplasmic reticulum/ER, and endomembrane Ca-ATPase, respectively. Protein names shown are preceded by genus and species initials. Arabidopsis (At) and rice (Os) ECA proteins are identified by their accession numbers in parentheses: AtECA1 (AAC68819; At1g07810), AtECA2 (CAA10659; At4g00900), AtECA3 (AAT68271; At1g10130), AtECA4 (AAD29957; At1g07670), OsECA1 (AAN64492; Os03g17310), OsECA2 (BAA90510; Os05g02940), and OsECA3 (ABF98693; Os03g52090). Other Ca2+ pumps aligned are Synechococcus elongatus SyoPacL (BAA03906); Saccharomyces cerevisiae ScPmr1 (P13586) and ScPmc1 (P38929); tomato LCA1 (Q42883); human (Hs) SERCA1 (O14983), SERCA2 (P16615), SERCA3 (Q93084), SPCA1 (AAH28139), and SPCA2 (AAV54193); Drosophila melanogaster (Dm) Ca-P60A (P22700) and SPoCk (AAN12202); and Oryctolagus cuniculus (rabbit) OcSERCA1a (PDB_ID 1SU4_A). The tree was aligned by T-Coffee. Values shown indicate the number of times (percent) that each branch topology was found in 1,000 replicates of the performed bootstrap analysis using PAUP* 4.0b10. B, Partial alignment of plant and other Ca2+-ATPases containing thapsigargin-interacting regions. Residue numbers correspond to rabbit SERCA1a or HsSERCA1. Black triangles indicate amino acid residues in direct contact with thapsigargin of rabbit SERCA1a (1SU4_A; Toyoshima and Nomura, 2002). Identical residues are shaded in black, while similar residues are boxed. TM3, TM5, and TM7 correspond to transmembrane regions of HsSERCA1. This alignment was generated in ESPript 2.2 (Gouet et al., 1999) using a T-Coffee-generated alignment. α-Helix, β-sheet, and turn are indicated as helix, black arrow, and T, respectively. The full alignment is shown in Supplemental Figure S1. ); however, only AtECA3 and OsECA3 shared higher identity (53%) with mammalian SERCA1a than with other members of the ECA subfamily (44.6%–45.1%). Intriguingly, none of the plant ECAs grouped with SPCA or secretory pathway Ca2+-ATPases (Pittman et al., 1999; Ton and Rao, 2004), which are represented by yeast Pmr1 and human SPCA (Fig. 1A). Sequence alignments revealed further insights. AtECA3 shared considerable amino acid sequence identity with transmembrane 3 (TM3), TM5, and TM7 of mammalian SERCA. The α-helices of TM3, TM5, and TM7 form the cavity that binds thapsigargin in the E2 conformation state of rabbit skeletal muscle SERCA (Toyoshima and Nomura, 2002). Interestingly, among the hydrophobic residues that face thapsigargin, Val-263, Val-773, and Phe-834 of rabbit OcSERCA (P04191) and human HsSERCA1 (O14983) are conserved and identical in the plant ECA3 from Arabidopsis and rice (Fig. 1B; Supplemental Fig. S1). In contrast, these residues are not found in yeast Pmr1p (SPCA) or AtECA1 (Fig. 1B), both of which are insensitive to thapsigargin (Liang and Sze, 1998). In addition, an extra tripeptide sequence, Q/HEA, corresponding to residues 240 and 241 of OcSERCA1, was present in most plant ECAs but not in ECA3. This analysis suggests that AtECA3 is distinct from other Arabidopsis ECAs and that plant ECA3-like proteins are structurally the most similar to animal ERCAs. AtECA3 Confers Tolerance of Yeast Growth on Medium with Low Ca2+ or High Mn2+ To determine the transport function of AtECA3 (or ECA3 for simplicity), a cDNA containing the complete open reading frame (ORF; AY650902) was cloned (see “Materials and Methods”) and expressed in yeast strain K616. The complete ORF of 2,994 bases encoded a protein of 997 residues. K616 is incapable of loading Ca2+ and Mn2+ into specific endomembrane compartments with high affinity (Cunningham and Fink, 1994), as it lacks a functional Golgi Ca2+/Mn2+ pump (Pmr1p) and a vacuolar Ca2+-ATPase (Pmc1), respectively. Therefore, growth of K616 is retarded or arrested when the culture medium contains submicromolar Ca2+ or toxic levels of Mn2+. However, the strain proliferates on medium containing high Ca2+ (0.1–1 mm) using Vcx1p, a vacuolar Ca2+/H+ exchanger that sequesters Ca2+ into endomembrane compartments (Cunningham and Fink, 1996). The K616 strain expressing AtECA3 grew slower than yeast expressing the empty p426 vector in synthetic complete (SC) medium containing no EGTA (Fig. 2A Figure 2. Open in new tabDownload slide AtECA3 confers tolerance to K616 yeast growth on medium depleted of Ca2+ or supplemented with Mn2+. A, Yeast growth on SC-URA medium with or without 5 mm EGTA. Seed culture was prepared in SC medium with 2% raffinose as carbon source. W303, the wild type, or mutant K616 (pmr1 pmc1 cnb1) harboring either AtECA3 under the GAL1 promoter or an empty vector was normalized to A 600 = 0.5. Cultures were serially diluted (five times), and 5 μL was spotted on plates containing 2% Gal and 10 mm MES-KOH at pH 6.25 and incubated for 3.5 d. B, ECA3 was less effective than ECA1 in promoting K616 yeast growth. Both ECA1 and ECA3 were expressed under the GAL1 promoter on a p426 vector. The method was as described for A. C, ECA3 confers yeast tolerance to 1 mm Mn2+. K616 mutant was transformed with an empty pDR196 vector or with pDR196 harboring AtECA3. Cells were serially diluted (10 times), spotted (10 μL) on medium containing 2% Glc and 10 mm MES-KOH at pH 6.25 alone (SC) or containing 1 mm Mn2+, and incubated for 7 d. Results from one representative experiment of three are shown. D, Sensitivity of ECA3-expressing K667 yeast to high Ca2+. K667 yeast was transformed with empty p426 vector, ECA1, or ECA3. Seed cultures were prepared in SC medium with 2% raffinose and then cultured in SC-URA medium containing 2% Gal (pH 5.5) and 10 mm MES-K. Cultures were serially diluted, spotted on medium containing either no addition (1 mm Ca2+) or with 150 mm CaCl2, and incubated for 6 d. Figure 2. Open in new tabDownload slide AtECA3 confers tolerance to K616 yeast growth on medium depleted of Ca2+ or supplemented with Mn2+. A, Yeast growth on SC-URA medium with or without 5 mm EGTA. Seed culture was prepared in SC medium with 2% raffinose as carbon source. W303, the wild type, or mutant K616 (pmr1 pmc1 cnb1) harboring either AtECA3 under the GAL1 promoter or an empty vector was normalized to A 600 = 0.5. Cultures were serially diluted (five times), and 5 μL was spotted on plates containing 2% Gal and 10 mm MES-KOH at pH 6.25 and incubated for 3.5 d. B, ECA3 was less effective than ECA1 in promoting K616 yeast growth. Both ECA1 and ECA3 were expressed under the GAL1 promoter on a p426 vector. The method was as described for A. C, ECA3 confers yeast tolerance to 1 mm Mn2+. K616 mutant was transformed with an empty pDR196 vector or with pDR196 harboring AtECA3. Cells were serially diluted (10 times), spotted (10 μL) on medium containing 2% Glc and 10 mm MES-KOH at pH 6.25 alone (SC) or containing 1 mm Mn2+, and incubated for 7 d. Results from one representative experiment of three are shown. D, Sensitivity of ECA3-expressing K667 yeast to high Ca2+. K667 yeast was transformed with empty p426 vector, ECA1, or ECA3. Seed cultures were prepared in SC medium with 2% raffinose and then cultured in SC-URA medium containing 2% Gal (pH 5.5) and 10 mm MES-K. Cultures were serially diluted, spotted on medium containing either no addition (1 mm Ca2+) or with 150 mm CaCl2, and incubated for 6 d. ). However, when free Ca2+ was reduced to approximately 0.8 μ m by 5 mm EGTA (Portzehl et al., 1964), growth of the K616 strain was severely curtailed. AtECA3 partially restored yeast K616 growth on Ca2+-depleted medium relative to wild-type cells (Fig. 2A). Curiously, under the same Gal1 promoter, AtECA3 was less effective than ECA1 (Fig. 2B) and AtECA4 (data not shown) in restoring mutant growth on Ca2+-depleted medium. AtECA1 rescued K616 growth in medium containing 10 mm EGTA, as shown before (Liang et al., 1997), while AtECA3 did not (data not shown). However, AtECA3 effectively restored mutant growth on medium containing 1 mm EGTA (Fig. 3 Figure 3. Open in new tabDownload slide AtECA3-GFP is active and exhibits intracellular localization in yeast. Yeast strain K616 hosting pDR196 vector alone or with ECA3-GFP was cultured on SC-URA with 10 mm MES-K+ at pH 6.25 alone or medium supplemented with 1 mm Mn2+ or 1 mm EGTA (6 d) as described for Figure 2. Confocal microscopy showed ECA3-GFP localized to intracellular membranes/organelles (Supplemental Fig. S2). Figure 3. Open in new tabDownload slide AtECA3-GFP is active and exhibits intracellular localization in yeast. Yeast strain K616 hosting pDR196 vector alone or with ECA3-GFP was cultured on SC-URA with 10 mm MES-K+ at pH 6.25 alone or medium supplemented with 1 mm Mn2+ or 1 mm EGTA (6 d) as described for Figure 2. Confocal microscopy showed ECA3-GFP localized to intracellular membranes/organelles (Supplemental Fig. S2). ), indicating that the two ECAs, although similar in transport activity, might differ in their kinetic properties, membrane localization, or expression level, as suggested below. We tested whether AtECA3 might support yeast growth at high Mn2+. AtECA3 expression under the Gal1 promoter on vector p426 failed to suppress the Mn2+ sensitivity of strain K616 (data not shown). Consequently, AtECA3 was expressed using pDR196, which contains a very strong constitutive promoter of the plasma membrane H+-ATPase1 (PMA1; Rentsch et al., 1995). Under the PMA1 promoter, AtECA3 expression improved K616 growth on medium containing 1 mm Mn2+ (Fig. 2C). This observation suggested that AtECA3 can also function as a Mn2+ pump to remove excess Mn2+ from the cytosol, similar to the ER-bound AtECA1 (Liang et al., 1997). To localize AtECA3 protein in yeast, a construct was made to generate a GFP fusion to the C terminus of AtECA3. Unlike other AtECAs, AtECA3 lacks a typical ER-retention motif, KxKxx, at its extreme C terminus, although it is rich in basic amino acid residues (KDRRDK). AtECA3-GFP fluorescence was observed in intracellular tubular and granular structures (Supplemental Fig. S2) that resembled the distribution of Pmr1p-GFP, a yeast Ca2+ pump localized to the ER and Golgi (Huh et al., 2003). The GFP-tagged protein restored the growth of K616 transformants on medium containing 1 mm EGTA or 1 mm Mn2+ (Fig. 3). These results indicate that the functionally active ECA3-GFP is localized to endomembranes in yeast. Identification and Analyses of T-DNA Insertional Mutants of AtECA3 To test the biological function of AtECA3 in planta, several T-DNA insertional lines (3-1, 3-4, and 3-5) were identified from the Salk collection (Alonso et al., 2003) and from Syngenta (McElver et al., 2001). Homozygous lines of each allele were obtained and their genotypes confirmed by PCR. Left border sequencing of the T-DNA was conducted to verify the insertion site of each allele (Fig. 4A Figure 4. Open in new tabDownload slide Three alleles of AtECA3 T-DNA insertional mutants were identified. A, Genomic structure of AtECA3 showing T-DNA insertion sites of eca3-1b, eca3-4, and eca3-5. The insertions were verified by left border sequencing. Bases in uppercase and lowercase letters indicate AtECA3 and T-DNA sequences, respectively. The left borders of T-DNA are indicated in black block arrows. B, RT-PCR shows the absence of full-length ECA3 transcripts in mutants. Total RNA from Col and mutant seedlings was reverse transcribed. Primers were used to amplify either ECA1 (positive control) or ECA3 by PCR. Col, Wild-type sibling lines. Primer pairs used to amplify regions upstream (E5′F and E5′R) or downstream (E3′F and E3′R) of T-DNA insertion sites are shown. Primer pair E3-15F and E3-15R was used to amplify the region flanking the T-DNA insertion of eca3-1b and eca3-5 mutants, and primers E3-4F and E3-4R were used to amplify eca3-4. Figure 4. Open in new tabDownload slide Three alleles of AtECA3 T-DNA insertional mutants were identified. A, Genomic structure of AtECA3 showing T-DNA insertion sites of eca3-1b, eca3-4, and eca3-5. The insertions were verified by left border sequencing. Bases in uppercase and lowercase letters indicate AtECA3 and T-DNA sequences, respectively. The left borders of T-DNA are indicated in black block arrows. B, RT-PCR shows the absence of full-length ECA3 transcripts in mutants. Total RNA from Col and mutant seedlings was reverse transcribed. Primers were used to amplify either ECA1 (positive control) or ECA3 by PCR. Col, Wild-type sibling lines. Primer pairs used to amplify regions upstream (E5′F and E5′R) or downstream (E3′F and E3′R) of T-DNA insertion sites are shown. Primer pair E3-15F and E3-15R was used to amplify the region flanking the T-DNA insertion of eca3-1b and eca3-5 mutants, and primers E3-4F and E3-4R were used to amplify eca3-4. ). Mutants Ateca3-5 and Ateca3-1b hosted T-DNA insertions in intron 11 and intron 12, respectively, while Ateca3-4 had an insertion in exon 18. To test for AtECA3 transcript, total RNA was extracted from 2-week-old wild-type and mutant plants grown on half-strength Murashige and Skoog (MS) medium (Fig. 4B) and reverse transcribed. Primers were designed to amplify any transcript upstream or downstream of the insertion site. Primers flanking the T-DNA insertion site and primer set E3′F and E3′R failed to amplify any product from all three mutants. Nevertheless, primers E5′F and E5′R amplified a product of 638 bp upstream of the insertion site in all three mutant alleles, indicating the presence of a truncated mRNA. Although the length of these transcripts is unclear, any potential translated protein would likely include only four TM regions (Lys-293) out of eight to 10 TM found in P-type 2A ATPases. A protein lacking a complete hydrophilic domain and TM5 to TM8 is unlikely to have any catalytic activity. These T-DNA insertional lines were used in phenotypic analyses as nonfunctional Ateca3 mutants. Siblings without T-DNA insertions from the same segregating population were used as wild-type controls. All three homozygous mutant lines were viable and completed their life cycle under normal conditions. No obvious growth or developmental defects were observed in the vegetative plants grown on soil. Role of AtECA3 in Root Growth Root Growth of eca3 Mutants Is Sensitive to High Mn2+ Our results suggested that calcium pump ECA3 also catalyzes the transport of Mn2+ into endomembrane compartments, as its expression in the yeast mutant K616 conferred tolerance to toxic levels of Mn2+ (1 mm; Fig. 2). So we examined the effect of Mn2+ levels on root growth. Plants were first grown in quarter-strength Hoagland nutrient medium containing from 3 to 100 μ m Mn2+. The root length of mutants was similar to that of wild-type plants in medium containing Mn2+ at 3.5 (Fig. 5A Figure 5. Open in new tabDownload slide Root growth of mutants is sensitive to 50 μ m Mn2+. A, Effect of Mn2+ on root growth in Hoagland medium. Arabidopsis seeds were germinated on quarter-strength Hoagland's medium containing 3.5 μ m Mn2+ and 2.5 mm Ca2+ (1% agar, 10 mm MES-K+, pH 5.7). Three days later, seedlings were transferred either to the same medium or to one supplemented with MnCl2 to 50 μ m. Photographs were taken 3 d after transfer. B, Effect of Mn2+ on root growth in half-strength MS medium. Arabidopsis seeds were germinated on half-strength MS medium containing 50 μ m Mn2+ with 1% Suc after 5 d of cold treatment. Seven-day-old seedlings were transferred to half-strength MS medium with 1% Suc containing 50 μ m or 0.1 mm Mn2+. Root length was scored 3 d after transfer. Six to 10 seedlings were measured in each treatment. Results represent three independent experiments. Error bars indicate se. C, Effect of Cu2+ on root growth in half-strength MS medium. Seeds were germinated as in B except that seedlings were transferred to half-strength MS medium alone (approximately 0.1 μ m Cu2+) or medium containing 10, 50, or 100 μ m Cu2+. Root lengths were scored 3 d after transfer. Six to 10 seedlings were measured in each treatment. Results represent three independent experiments. Error bars indicate se. Figure 5. Open in new tabDownload slide Root growth of mutants is sensitive to 50 μ m Mn2+. A, Effect of Mn2+ on root growth in Hoagland medium. Arabidopsis seeds were germinated on quarter-strength Hoagland's medium containing 3.5 μ m Mn2+ and 2.5 mm Ca2+ (1% agar, 10 mm MES-K+, pH 5.7). Three days later, seedlings were transferred either to the same medium or to one supplemented with MnCl2 to 50 μ m. Photographs were taken 3 d after transfer. B, Effect of Mn2+ on root growth in half-strength MS medium. Arabidopsis seeds were germinated on half-strength MS medium containing 50 μ m Mn2+ with 1% Suc after 5 d of cold treatment. Seven-day-old seedlings were transferred to half-strength MS medium with 1% Suc containing 50 μ m or 0.1 mm Mn2+. Root length was scored 3 d after transfer. Six to 10 seedlings were measured in each treatment. Results represent three independent experiments. Error bars indicate se. C, Effect of Cu2+ on root growth in half-strength MS medium. Seeds were germinated as in B except that seedlings were transferred to half-strength MS medium alone (approximately 0.1 μ m Cu2+) or medium containing 10, 50, or 100 μ m Cu2+. Root lengths were scored 3 d after transfer. Six to 10 seedlings were measured in each treatment. Results represent three independent experiments. Error bars indicate se. ), 10, or 20 μ m (data not shown). But root growth of eca3-4 was clearly reduced compared with that of wild-type plants when Mn2+ was elevated to 50 μ m. Moreover, mutants manifested little or no lateral roots after 3 d of growth, suggesting inhibition of lateral root initiation. The compromised root growth also caused changes in shoot growth, such as reduced leaf expansion and rosette size (data not shown). Therefore, as in yeast, AtECA3 conferred tolerance to high Mn2+ in plants. Similar results were obtained when plants were nourished by half-strength MS medium, which contains 50 μ m Mn2+. Primary roots of wild-type plants grew, but eca3-4 mutant growth was inhibited (Fig. 5B). Wild-type plants also became sensitive when Mn2+ was increased to 100 μ m (Fig. 5B). It is noted that a concentration of 50 μ m Mn2+ in half-strength MS medium is considered unusually high compared with a recommended Mn2+ of less than 10 μ m in Hoagland's nutrient medium (Hoagland and Arnon, 1950). Therefore, 50 μ m probably imposes a Mn2+ stress that is tolerated by the wild type but not by mutant seedlings. In contrast, increasing Cu2+ inhibited the root growth of both wild-type and eca3-4 plants similarly (Fig. 5C). These results indicate that AtECA3 could alleviate Mn2+ toxicity through a mechanism distinct from that which guards against Cu2+ toxicity, another essential yet potentially toxic divalent heavy metal. These results are consistent with the notion that AtECA3 transports Mn2+ but is not involved in transporting Cu2+. Ca-Stimulated Root Growth Is Reduced in eca3 Mutants Ca2+ at a few millimolar concentration is required for root growth (Marschner, 1995), so we tested the effect of Ca2+ on root growth in mutant lines containing a T-DNA insertion in the AtECA3 gene. The effect of external Ca2+ on root growth in wild-type seedlings was first tested using half-strength MS medium in which the Ca2+ concentration was specifically varied. Calcium at 3 mm stimulated root growth (Fig. 6B Figure 6. Open in new tabDownload slide Ca2+-stimulated root growth is abolished in Ateca3 mutants. A, A representative image of Ateca3-4 and its wild-type (Col) seedlings. Wild-type and mutant seeds were germinated side by side on plates containing half-strength MS medium with 3 mm Ca2+. Photographs were taken at 3 d. B, Effect of Ca2+ concentration. Seeds from wild-type (black circles), eca3-1b (white circles), and eca3-4 (white triangles) plants were germinated on plates containing half-strength MS with either no added Ca2+ or supplemented with Ca2+ to final concentrations of 0.1, 3, and 20 mm. Each experiment consisted of 20 seedlings per treatment. Primary root length was measured at 3 to 4 d. Data represent at least three independent experiments. Error bars indicate se. C, Differential effect of Ca2+ on root growth of eca3 and eca1 mutants. Seeds from wild-type (Col), eca3-1b, eca3-4, eca3-5, wild-type (Wassilewskija [WS]), eca1-1, and 35S-ECA1 (Wu et al., 2002) plants were germinated on plates containing half-strength MS with 3 mm Ca2+. Each experiment consisted of 12 to 18 seedlings per treatment. Primary root length was measured at 4 d. Data represent at least two independent experiments. Error bars indicate se. [See online article for color version of this figure.] Figure 6. Open in new tabDownload slide Ca2+-stimulated root growth is abolished in Ateca3 mutants. A, A representative image of Ateca3-4 and its wild-type (Col) seedlings. Wild-type and mutant seeds were germinated side by side on plates containing half-strength MS medium with 3 mm Ca2+. Photographs were taken at 3 d. B, Effect of Ca2+ concentration. Seeds from wild-type (black circles), eca3-1b (white circles), and eca3-4 (white triangles) plants were germinated on plates containing half-strength MS with either no added Ca2+ or supplemented with Ca2+ to final concentrations of 0.1, 3, and 20 mm. Each experiment consisted of 20 seedlings per treatment. Primary root length was measured at 3 to 4 d. Data represent at least three independent experiments. Error bars indicate se. C, Differential effect of Ca2+ on root growth of eca3 and eca1 mutants. Seeds from wild-type (Col), eca3-1b, eca3-4, eca3-5, wild-type (Wassilewskija [WS]), eca1-1, and 35S-ECA1 (Wu et al., 2002) plants were germinated on plates containing half-strength MS with 3 mm Ca2+. Each experiment consisted of 12 to 18 seedlings per treatment. Primary root length was measured at 4 d. Data represent at least two independent experiments. Error bars indicate se. [See online article for color version of this figure.] ), as shown before (Marschner 1995). Reduced root length at 0.1 mm or less Ca2+ confirmed that this level of Ca2+ limited growth. Similarly, root growth at 20 mm Ca2+ was decreased, demonstrating that excess Ca2+ was stressful to the seedling (Fig. 6B). Intriguingly, the 3 mm Ca2+-stimulated root growth was not observed in eca3-1b or eca3-4 mutants (Fig. 6B), indicating that mutants were nearly insensitive to the beneficial effects of Ca2+. Similar results were observed in the eca3-5 mutant (Fig. 6C). At 3 mm Ca2+, root lengths of eca3-1b and eca3-4 mutants were reduced by 33% and 34%, respectively, compared with wild-type controls. With 3 mm external Ca2+, it is reasonable to assume that Ca2+ entry pathways via cation-permeable channels are functional in eca3 mutants. Thus, the results indicate that reduced growth is due to defective sorting of cytosolic Ca2+ into one or more intracellular compartments or organelles. Spatial Expression of AtECA3 in Root and Leaf The tissue-specific pattern of expression for AtECA3 was examined by GUS reporter activity driven by a 5-kb intergenic region upstream of the ORF. In vegetative tissues, AtECA3 promoter∷GUS activity was enriched in vascular tissues of primary roots (Fig. 7A Figure 7. Open in new tabDownload slide Expression of AtECA3 promoter∷GUS in vascular tissues. Transgenic plants hosting the 5.2-kb AtECA3 promoter∷GUS construct were grown on half-strength MS medium or on soil. Whole seedlings, plants, or organs were incubated in X-Gluc for 2 d. GUS activity was detected in the vascular tissues of the primary root (A), lateral root (B), and true leaves (E) of 14-d-old plants but not in cotyledon, shoot apex, or hypocotyl of 3-d-old seedlings (C and D). Activity was also detected in vascular tissues of the floral pedicel (F and G) and the style (H). Bars = 100 μm. Figure 7. Open in new tabDownload slide Expression of AtECA3 promoter∷GUS in vascular tissues. Transgenic plants hosting the 5.2-kb AtECA3 promoter∷GUS construct were grown on half-strength MS medium or on soil. Whole seedlings, plants, or organs were incubated in X-Gluc for 2 d. GUS activity was detected in the vascular tissues of the primary root (A), lateral root (B), and true leaves (E) of 14-d-old plants but not in cotyledon, shoot apex, or hypocotyl of 3-d-old seedlings (C and D). Activity was also detected in vascular tissues of the floral pedicel (F and G) and the style (H). Bars = 100 μm. ), lateral roots (Fig. 7B), and young expanding leaves (Fig. 7E). At the root tip, GUS activity first appeared in the elongation and differentiation zones (Fig. 7, A and B) but was not detectable in the cell division zone under the conditions tested. GUS activity was not detected in the shoot apex (Fig. 7, C and D) or in fully expanded cotyledons (Fig. 7D). Promoter activity was also detected in vascular tissues of floral pedicels and of the style (Fig. 7, F–H). Expression of AtECA3 in other cell types is not excluded by this analysis, as the GUS gene was transcriptionally fused to the 5′ regulatory region only, so that any transcriptional regulation by cis-acting elements within introns would be missed, as would 3′ or chromosomal positional effects. RT-PCR of total RNA verified the presence of AtECA3 transcripts in root and leaf (Li, 2006). Using a smaller 1.5-kb promoter fragment upstream of AtECA3, Mills et al. (2008) showed that expression in vascular tissues was enriched in xylem parenchyma and the pericyle. In addition, GUS activity was detected in root caps, hydathodes, and guard cells (Mills et al., 2008). Thus, although minor differences exist in the two studies, the results using either a 1.5- or 5-kb promoter show similarities that are supported in general by whole genome ATH1 chip data (http://www.geneinvestigator.ethz.ch). The AtECA3 promoter activity appeared to be lower than that of AtECA1 or AtECA4 based on 2 d of 5-bromo-4-chloro-3-indolyl β-d-glucuronide (X-Gluc) staining required to visualize GUS activity. In contrast, AtECA1 promoter∷GUS activity was detected after 3 h of incubation in X-Gluc in roots and leaves, including the root tip, lateral roots, vascular tissues, ground tissues, and guard cells (Supplemental Fig. S3). The higher expression of AtECA1 relative to AtECA3 is supported by the root expression map from the Benfey laboratory (Supplemental Fig. S4). Together, these results confirm that AtECA3 is expressed in all cell types found in roots but that its expression is consistently much lower than that of AtECA1. AtECA3-GFP Is Localized with Endosome/PVC Markers in Plant Cells Although functional studies from yeast and plants suggest that AtECA3 is localized to endomembrane compartments, the identity of the compartment is unclear. We determined the membrane location of AtECA3 after transient expression using the S35 cauliflower mosaic virus (CaMV) promoter in Arabidopsis mesophyll protoplasts (Jin et al., 2001; Kim et al., 2001). We first demonstrated that the AtECA3 fused at the C terminus to GFP retained native activity, judging by its ability to restore yeast mutant growth on Ca2+-depleted medium or medium containing toxic levels of Mn2+ (Fig. 3). Cells expressing ECA3-GFP alone (Fig. 8Ae Figure 8. Open in new tabDownload slide Localization of AtECA3-GFP to endosomes. A, Differential patterns of AtECA1, AtECA3, and GFP-tagged markers transiently expressed in mesophyll protoplasts. Arabidopsis leaf protoplasts were transfected separately with a single GFP construct driven by the 35S CaMV promoter. After 18 to 24 h of incubation, GFP signal was observed by confocal microscopy in cells transfected with AtECA1-GFP (a), free soluble eGFP (b), ER retention sequence GFP-HDEL (c), vacuolar syntaxin GFP-AtSyp22 (d), AtECA3-GFP (e), trans-Golgi enzyme sialyl transferase ST-GFP (f), trans-Golgi network syntaxin GFP-AtSyp41 (g), and endosomal Rab-GTPase GFP-Ara7 (h). Bars = 5 μm. Panels reflect representative images from three to six independent experiments. B, ECA3-GFP is associated with a population of endosomes. Arabidopsis leaf protoplasts were cotransfected with ECA3-GFP and a marker protein tagged with RFP. After 18 to 24 h of incubation, fluorescent signals were observed. Markers used are Golgi ST-RFP (a), trans-Golgi network RFP-Syp41 (b), and endosomal RFP-Ara7 (c). Corresponding cells coexpressing ECA3-GFP are shown in a′, b′, and c′ (column 2). Merged image (column 3) c″ shows AtECA3 colocalized partially with Ara7. Bright-field images of the cells are shown at far right (column 4). Bars = 5 μm. Figure 8. Open in new tabDownload slide Localization of AtECA3-GFP to endosomes. A, Differential patterns of AtECA1, AtECA3, and GFP-tagged markers transiently expressed in mesophyll protoplasts. Arabidopsis leaf protoplasts were transfected separately with a single GFP construct driven by the 35S CaMV promoter. After 18 to 24 h of incubation, GFP signal was observed by confocal microscopy in cells transfected with AtECA1-GFP (a), free soluble eGFP (b), ER retention sequence GFP-HDEL (c), vacuolar syntaxin GFP-AtSyp22 (d), AtECA3-GFP (e), trans-Golgi enzyme sialyl transferase ST-GFP (f), trans-Golgi network syntaxin GFP-AtSyp41 (g), and endosomal Rab-GTPase GFP-Ara7 (h). Bars = 5 μm. Panels reflect representative images from three to six independent experiments. B, ECA3-GFP is associated with a population of endosomes. Arabidopsis leaf protoplasts were cotransfected with ECA3-GFP and a marker protein tagged with RFP. After 18 to 24 h of incubation, fluorescent signals were observed. Markers used are Golgi ST-RFP (a), trans-Golgi network RFP-Syp41 (b), and endosomal RFP-Ara7 (c). Corresponding cells coexpressing ECA3-GFP are shown in a′, b′, and c′ (column 2). Merged image (column 3) c″ shows AtECA3 colocalized partially with Ara7. Bright-field images of the cells are shown at far right (column 4). Bars = 5 μm. ) had small punctate fluorescence that resembled the puncta seen in Golgi or post-Golgi compartment markers (Fig. 8A, f–h), including sialyl transferase, Syp41, or Ara7 (Ueda et al., 2004; Uemura et al., 2004). The puncta from ECA3-GFP were dissimilar from those emitted from the ER or a vacuolar marker (Syp22). A GFP tag at the C terminus apparently did not interfere with potential retention signals for another calcium pump, as AtECA1 tagged with GFP at the C terminus gave a reticulate fluorescent pattern characteristic of ER when it was transiently expressed in protoplasts (Fig. 8Aa). AtECA1 was previously localized to the ER by cell fractionation and immunostaining (Liang et al., 1997). To clarify the membrane location, ECA3-GFP was coexpressed with markers tagged with a red fluorescent protein (RFP) in protoplasts. The fluorescence signals were carefully collected with a Zeiss LSM 510 confocal microscope using different emission wavelengths. ECA3-GFP did not colocalize with ST-RFP or with RFP-Syp41 (Fig. 8B), which are markers for the trans-Golgi or the trans-Golgi network, respectively (Ueda et al. 2001, 2004). ECA3-GFP colocalized in part with RFP-Ara7, an endosome/PVC marker (Lee et al., 2004; Ueda et al., 2004), as indicated by the extent of yellow fluorescence in merged images (Fig. 8Bc″). These results suggest that ECA3-GFP is localized to a subpopulation of post-Golgi compartments, including endosomes and PVCs. Enhanced Apoplastic Peroxidase Activity and Protein Secretion in eca3 Mutants Because plant post-Golgi compartments are involved in the processing, sorting, and exocytosis of proteins, we wondered whether secretory activities might be compromised in eca3 mutants. The activities of secreted apoplastic peroxidases (APXs) were examined in roots from hydroponically grown plants. Apoplastic washing fluid (AWF) was extracted from roots by first vacuum infiltrating the tissue with buffer and then collecting the fluid by centrifugation. Guaiacol-dependent peroxidase activity was then monitored spectrophotometrically by following the oxidation of guaiacol by hydrogen peroxide to form tetraguaiacol. We first established that the enzyme reaction, monitored by the appearance of tetraguaiacol, was linear for 2 min (Fig. 9A Figure 9. Open in new tabDownload slide APX activity of wild-type and Ateca3 plants. A, Time course of guaiacol oxidation by root AWF. AWF was extracted from wild-type and mutant roots of similar fresh weight. The reaction was started by adding guaiacol to a reaction mixture containing 20 μL of AWF from the mutant (white circles) or the wild type (black circles). Data show the change in A 470 due to tetraguaiacol formation from a single experiment representative of three. B, Rate of guaiacol oxidation as a function of AWF volume is linear. AWF extracted from the wild type (black circles) and eca3-4 (white circles) was assayed for peroxidase activity. The change in optical density is plotted as a function of AWF volume. A regression equation showed a linear relationship where R 2 is 0.95 or 0.99 for wild-type or mutant AWF. The slopes were used to calculate guaiacol-dependent APX activity. Data are from one representative experiment of three. Figure 9. Open in new tabDownload slide APX activity of wild-type and Ateca3 plants. A, Time course of guaiacol oxidation by root AWF. AWF was extracted from wild-type and mutant roots of similar fresh weight. The reaction was started by adding guaiacol to a reaction mixture containing 20 μL of AWF from the mutant (white circles) or the wild type (black circles). Data show the change in A 470 due to tetraguaiacol formation from a single experiment representative of three. B, Rate of guaiacol oxidation as a function of AWF volume is linear. AWF extracted from the wild type (black circles) and eca3-4 (white circles) was assayed for peroxidase activity. The change in optical density is plotted as a function of AWF volume. A regression equation showed a linear relationship where R 2 is 0.95 or 0.99 for wild-type or mutant AWF. The slopes were used to calculate guaiacol-dependent APX activity. Data are from one representative experiment of three. ). The initial rate of the reaction was then estimated from the slope. Increasing aliquots of AWF from wild-type roots produced an enhanced rate of guaiacol oxidation, indicating that Arabidopsis roots contained extracellular peroxidase activity (Fig. 9B). Based on four independent experiments, the extracellular peroxidase activity of wild-type roots was estimated to be 79 nmol min−1 g−1 fresh weight of root. When AWF of mutants was analyzed, an increase in APX was consistently observed when activity was expressed per gram fresh weight of roots. The APX activity of eca3-4 mutants was approximately 147 nmol min−1 g−1 fresh weight of root. In three independent experiments, the activity of the mutants was 80%, 86%, and 86% higher than that of wild-type controls (Fig. 10 Figure 10. Open in new tabDownload slide AWF of mutants defective in the endosomal Ca2+ pump showed increased protein and peroxidase activity. AWF was extracted from wild-type and eca3-4 roots of equivalent mass (fresh weight) in each experiment. Wild-type plants showed an average of 111 μg protein mL−1 AWF (100%) and 261 nmol tetraguaiacol formed min−1 mL−1 AWF (100%). Specific APX activity is expressed as nanomoles per minute per microgram of protein. Peroxidase activity and protein amount per tissue fresh weight were 76 nmol min−1 g−1 fresh weight (100%) and 28 μg protein g−1 fresh weight (100%) in wild-type plants. Data represent averages of three independent experiments. Error bars indicate sd. [See online article for color version of this figure.] Figure 10. Open in new tabDownload slide AWF of mutants defective in the endosomal Ca2+ pump showed increased protein and peroxidase activity. AWF was extracted from wild-type and eca3-4 roots of equivalent mass (fresh weight) in each experiment. Wild-type plants showed an average of 111 μg protein mL−1 AWF (100%) and 261 nmol tetraguaiacol formed min−1 mL−1 AWF (100%). Specific APX activity is expressed as nanomoles per minute per microgram of protein. Peroxidase activity and protein amount per tissue fresh weight were 76 nmol min−1 g−1 fresh weight (100%) and 28 μg protein g−1 fresh weight (100%) in wild-type plants. Data represent averages of three independent experiments. Error bars indicate sd. [See online article for color version of this figure.] ). The increase in activity was accompanied by an increased amount of apoplastic protein by the mutants. eca3-4 mutant roots produced 39%, 60%, and 95% (in three separate experiments) more protein per gram fresh weight of tissue than did wild-type roots. Similar results were obtained with the eca3-5 mutant, which produced 2-fold more apoplastic protein than did wild-type roots (data not shown). Thus, the specific activity of peroxidase (nanomoles per minute per microgram of protein) was relatively unchanged in the apoplastic fluid between the wild type and mutants. Interestingly, the increase in both activity and protein in the mutants was still detected when they were based on milliliters of AWF (Fig. 10). These results indicate that the concentration of protein and peroxidase was increased in the extracellular fluid of mutants. The volume of fluid collected per gram fresh weight of tissue was quite similar, although slightly more (19%) was recovered from the mutant than from the wild type. Together, these results suggest that the secretory process of the eca3 mutant is altered, causing an increase in total apoplastic protein and a proportional increase in the activity of secreted peroxidase activity. DISCUSSION Maintaining divalent cation homeostasis for plant growth and adaptation depends on a remarkable coordination of transport activities; however, the cellular and biochemical bases of Ca2+ and Mn2+ distribution and their dynamics in plants are still poorly understood. Here, we provide evidence for a special endosomal Ca2+/Mn2+ pump that is involved in multiple functions, including the secretory process, root growth, and ion detoxification. Phylogenetic analyses revealed that of four ECAs in Arabidopsis, ECA3 represents a unique subbranch and showed the highest identity and structural similarities to the subfamily of animal SERCA Ca2+-ATPase. This unique ECA3 subgroup is conserved among higher plants, as shown by the high identity/similarity (79%/87.3%) of Arabidopsis ECA3 (At1g17310) with rice (japonica) ECA3 (Os03g52090). Moreover, like Arabidopsis, only one ECA3-like gene is found in the rice genome, strongly suggesting that this ion pump is functionally conserved in flowering plants. AtECA3 Is a Ca2+/Mn2+-ATPase Functionally Distinct from AtECA1 We provide evidence that AtECA3 behaves like a Ca2+/Mn2+ pump, as it functionally replaced two endogenous Ca2+ pumps of yeast, Pmr1 and Pmc1p, localized on the Golgi/ER and vacuole, respectively. AtECA3 restored the ability of strain K616 to grow on Ca2+-depleted medium. As AtECA3 is localized to endomembranes in yeast, these results (Fig. 2) are consistent with the idea that AtECA3 loads Ca2+ into endomembrane compartments and that the accumulated Ca2+ activates processes needed for growth. AtECA3 also conferred tolerance of K616 yeast to toxic levels of Mn2+, suggesting that the pump is able to remove Mn2+ from the cytosol. These results of AtECA3 activity are consistent with those reported by Mills et al. (2008). Thus, biochemically, AtECA3 appears very similar to AtECA1 (Liang et al., 1997). We showed before that AtECA1 pumps 45Ca2+ with selectivity for divalent cations, like Mn2+ (Liang and Sze, 1998; Wu et al., 2002). However, several observations suggest that AtECA3 differs in properties and function from AtECA1. First, AtECA1 was more effective than AtECA3 in promoting the growth of the K616 mutant on Ca2+-depleted medium containing 5 mm EGTA (Fig. 2B). Second, AtECA3 expression in strain K667 caused a hypersensitive response to 150 mm Ca2+, whereas AtECA1 expression had no effect (Fig. 2D). Strain K667 has a functional Pmr1p but is defective in the vacuolar Ca2+/H+ exchanger (Vcx1) and the vacuolar Ca2+-ATPase (Pmc1); thus, the strain is highly sensitive to very high levels of Ca2+ (Cunningham and Fink, 1994). Reduced K667 yeast growth by expression of AtECA3, but not by AtECA1, suggests that AtECA3 attenuated Pmr1p activity. Although the mechanism is unknown at this time, AtECA1 and AtECA3 clearly affect K667 yeast growth differentially. Thus, the function of AtECA3 in yeast appeared to be distinct from that of AtECA1, possibly due to distinct subcellular locations, as shown for plants. This idea is further supported by the differential phenotype of the T-DNA insertional mutants in plants. For example, root growth of the eca1-1 mutant was similar to that of the wild type at 1.5 mm (Wu et al., 2002) or 3 mm external Ca2+ (Fig. 6C); however, three alleles of eca3 displayed reduced root growth. AtECA3 Encodes an Endosomal Ca2+/Mn2+ Pump Our studies suggest that AtECA3 is a Ca2+/Mn2+ pump associated with plant endosomal membranes. We showed that AtECA3 fused at the C terminus to GFP retained its activity as a Ca2+ as well as a Mn2+ pump (Fig. 3) in yeast. AtECA3-GFP, expressed transiently in mesophyll protoplasts, emitted punctate fluorescent patterns initially thought to resemble Golgi compartments (Li, 2006), as reported by Mills et al. (2008). However, in further studies, the AtECA3-GFP signal did not colocalize with markers of the trans-Golgi (sialyltransferase) or the trans-Golgi network (Syp41; Fig. 8B). Instead AtECA3-GFP partially colocalized with an endosome/PVC marker, Ara7. Ara7 is a conventional-type ortholog of Rab5, a Rab GTPase involved in regulating vesicular transport in the endocytic pathway of mammalian cells. In Arabidopsis cells, Ara7 was shown to be associated with earlier endocytic compartments involved in recycling plasma membrane proteins (Ueda et al., 2004). However, another study suggested that Ara7 localized to the PVC (Lee et al., 2004). Thus, these studies to localize AtECA3 suggest that the Ca2+/Mn2+ pump is associated with vesicles involved in one or more possible functions, including maturation/differentiation of the trans-Golgi network, protein sorting at the PVC, machinery (e.g. cytoskeletal dynamics) involved in vesicle trafficking, and events that promote membrane fusion, secretion, or exocytosis to the plasma membrane or vacuole (Samaj et al., 2005). In other experiments, we observed AtECA3-GFP protein localized to cortical structures at the tip of growing pollen tubes (data not shown). This distribution pattern resembles that of secretory vesicles and Golgi-derived compartments that readily fuse with the plasma membrane during fast pollen tube growth. These results together are consistent with the idea that AtECA3 is located on endosomal membranes, including those involved in endocytosis and/or exocytosis in plant cells. Previously, a Golgi-purified fraction from pea (Pisum sativum) epicotyl was shown to have Ca2+ pump activity (Ordenes et al., 2002), although without sequence information it is unclear whether the pea pump is orthologous to AtECA3. Whether the subcellular distribution of AtECA3-GFP is predominantly Golgi alone (Mills et al., 2008), post-Golgi (Fig. 8), or varies according to the physiological state of the cell will need further investigation. However, it is clear that the punctate pattern of AtECA3-GFP is strikingly distinct from the reticulate pattern of AtECA1-GFP, indicating that these two pumps are localized to separate compartments. Possible Roles of Endosomal Ca2+ and Mn2+ in Vesicle Trafficking and Secretion Intriguingly, we found that eca3 mutants secreted more total protein and more peroxidase activity than wild-type plants (Figs. 9 and 10), suggesting that perturbation of Ca2+ and/or Mn2+ homeostasis in the endosomes perturbs protein secretion. Coincidently, yeast mutants lacking Pmr1 also secrete more proteins than wild-type cells (Smith et al., 1985; Rudolph et al., 1989), although the mechanism remains unclear. In plants, Ca2+ mediated the association of the vacuolar sorting receptor, VSR1, to its cargo. Furthermore, a defective VSR1 causes vacuolar storage proteins to be secreted (Shimada et al., 2003). Here, we provide genetic evidence linking endosomal Ca2+ homeostasis to protein secretion in plants. It is not yet understood why a defect in AtECA3 function would increase the secretion of peroxidase. Secreted peroxidases (class III) or apoplastic peroxidases include many isoforms and are involved in diverse functions, such as generating reactive oxygen species, forming cell wall polymers, and regulating hydrogen peroxide levels. They modify cell wall properties, such as loosening walls during growth and cross-linking walls to form a barrier in response to wounding, biotic, and abiotic stress. Interestingly, peroxidases and phenolic compounds are induced by heavy metals and appear to protect plants from heavy metal toxicity (Passardi et al., 2005). Increased peroxidases might aid in cross-linking cell walls and thus reduce or arrest wall growth. Possibly, deregulated secretion might alter cell wall composition or organization in eca3 mutants. Function of an Endosomal Ca2+ in Root Growth Almost nothing is known about the role of endosomal Ca2+ pumps in plants. Here, we show that the Ca2+-stimulated root growth seen in wild-type plants is reduced or inhibited in eca3 mutants. In contrast, the external concentration (millimolar) of [Ca2+]ext had no effect on the growth of the eca1-1 mutant (Wu et al., 2002). Ca2+ entry into the eca3 mutant should not be limited when external Ca2+ is 3 mm. This idea is supported by the similar Ca2+ content of eca3 and wild-type plants (Mills et al., 2008). Thus, the requirement for millimolar levels of Ca2+ for root growth in wild-type plants indicates that sorting internal Ca2+ into particular endosomal compartments, like post-Golgi compartments, restricts the growth of mutants. We suggest that AtECA3 promotes growth by loading an adequate level of Ca2+ into a subpopulation of endosomal compartments. The sequestered Ca2+ could perform one or more functions, such as (1) to modulate enzyme or protein activities in the lumen, (2) to fill Ca2+ stores that can be released via gated Ca2+ channels to enhance local [Ca2+]cyt in a temporal manner, and (3) to supply Ca2+ to the extracellular medium for biochemical, signaling, or polarity purposes. Endosomal luminal [Ca2+]lum might modulate protein and enzyme activities that are responsible for vesicle transport or for modification of its polysaccharide and protein cargo. An induced local rise in [Ca2+]cyt may aid (1) in directing the movement of secretory vesicles via the cytoskeleton to their destination and (2) in modulating exocytosis, including membrane docking and fusion events, and perhaps subsequent endocytosis to recycle essential components of secretory pathways. Studies using yeast and animal cells have shown that Ca2+ in the Golgi and Golgi-derived vesicles has roles in protein processing, sorting, glycosylation, secretion (Durr et al., 1998; Ton et al., 2002; Rizzuto and Pozzan, 2006), and, more recently, Ca2+ signaling (Van Baelen et al., 2004). In plants, the vacuolar sorting receptor (AtVSR1 or pumpkin [Cucurbita pepo] VP72) binds its cargo in a Ca-dependent manner (Watanabe et al., 2002; Shimada et al., 2003). Thus, depleting luminal Ca2+ concentration in plant endosomes would conceivably disrupt sorting and the synthesis and delivery of wall proteins and noncellulosic polysaccharides (Nebenfuhr and Staehelin, 2001; Robinson, 2003) and therefore affect polarized growth and cell patterning. Role of AtECA3 in Detoxifying Excess Mn2+ While a few micromolar Mn2+ in the soil is sufficient to sustain plant growth (Marschner, 1995), high Mn2+ is detrimental. We show that AtECA3 plays a role in Mn2+ detoxification in both yeast and Arabidopsis seedlings, based on the sensitivity of eca3 mutants to high Mn2+(Fig. 2). Curiously, Mills et al. (2008) did not see evidence for a role of ECA3 in detoxifying excess Mn2+ in plants, which was inconsistent with their yeast result, where AtECA3 conferred tolerance to high Mn2+ in the K616 mutant. The difference between their findings and our results showing a Mn-sensitive eca3 mutant plant phenotype is most likely due to the experimental conditions used in the two studies. Importantly, Mills et al. (2008) showed that ECA3 is critical for Mn2+ nutrition in plants. They found that 9-d-old eca3-2 mutants (SALK_0570619) had reduced fresh weight when grown on Mn2+-deficient medium and that a few micromolar Mn2+ restored growth to wild-type levels. Taken together, these results suggest that ECA3 serves at least two biological functions: (1) to accumulate Mn2+ into a Golgi-related compartment to satisfy Mn2+ nutrition needed for growth; and (2) to load Mn2+ into a subset of post-Golgi compartments that participate in detoxifying excess Mn2+. The cellular basis of detoxification is unclear. Curiously, the presence of AtECA1, an abundant divalent cation transporter, is inadequate to reduce Mn2+ toxicity in eca3 mutants when [Mn2+]ext is 50 μ m or greater. As AtECA1 pumps Mn2+ and Ca2+ mainly into the ER lumen, a relatively extensive endomembrane system, the impaired growth is unlikely caused by an inability to lower cytosolic [Mn2+]cyt by divalent pumps or H+-coupled cotransporters into ER or vacuolar compartments (Sze et al., 2000). Instead, the machinery to alleviate Mn2+ toxicity is dependent on the proper functioning of additional endomembranes, such as the PVC and endosomal vesicles. It is possible that inadequate loading of Ca2+, Mn2+, or both into endosomes causes protein missorting and deregulated membrane trafficking in eca3, as shown by increased apoplastic peroxidase, and thus interferes with the detoxification machinery that might involve one or more processes, including delivering Mn2+ into vacuoles and the release of Mn2+ and stress-induced proteins into the apoplast (Fecht-Christoffers et al., 2006). It is possible that Mn2+ entering the cytosol is pumped into the ER by AtECA1 and then removed by exocytosis via endosomes with AtECA3. Summary and Model The apparently distinct physiological effects of an endosomal cation pump, AtECA3, in Ca2+-stimulated root growth, in Mn2+ nutrition, and in Mn2+ detoxification appear to converge on the highly regulated endosomal trafficking pathway and secretory processes of cells. When Ca2+ and Mn2+ are present at near optimal range, loading of these divalent cations into endosomal compartments promotes growth, possibly through the synthesis and delivery of wall proteins and polysaccharides. When wild-type plants are subjected to Mn2+ toxicity stress, the endosomal/secretory trafficking machinery is likely engaged in the dynamic process of moving excess Mn2+ either to or from the vacuole and/or to the cell exterior. Taken together, the results of this study suggest that loading Ca2+ and Mn2+ into a subpopulation of post-Golgi compartments by AtECA3 affects activities critical for highly regulated endosomal trafficking that determine intracellular sorting (to and from the vacuole) and the extent of exocytosis and secretion. Given the central role of membrane trafficking in plant responses to hormones and to stress, it is very likely that AtECA3 will affect many other growth and developmental processes. MATERIALS AND METHODS Plant Materials, Growth, and Measurement Wild-type and eca3 Arabidopsis (Arabidopsis thaliana) plants (Columbia [Col] ecotype) were used in this study. Homozygous seed stocks for eca3-1b, eca3-4, and eca3-5 correspond to SAIL_557_C07, SALK_032802, and SALK_045567 lines, respectively (McElver et al., 2001; Alonso et al., 2003). For growth on plates, Arabidopsis seeds were surface sterilized by soaking in 20% (v/v) Clorox and 0.05% Tween 20 for 10 min followed by five rinses in sterile water. The seeds were placed on half-strength MS medium (Murashige and Skoog, 1962) containing 0.8% agar and 2.5 mm MES-K at pH 5.7, followed by stratification at 4°C for 3 d in the dark. The plates were then positioned vertically in Conviron ATC60 growth chambers with a photoperiod of 16 h of light under an illumination of 120 to 180 μE m−2 s−1 and 8 h of dark. The temperature was set at 22°C in the day and 20°C at night. For soil-grown plants, Arabidopsis seeds were planted on synthetic soil mixture containing Miracle-Gro potting mix and perlite, followed by 3 d at 4°C in the dark, before being taken to growth chambers with a photoperiod of 16 h of light of 120 to 180 μE m−2 s−1 at 22°C and 8 h of dark at 20°C and 60% relative humidity, or with a short-day photoperiod of 10 to 12 h of light of 120 μE m−2 s−1. Plants were watered twice per week or as needed. Wild-type and mutant plants were always grown side by side in the same tray and growth chamber for consistency. Root Length Measurement Three days after germination on square plates containing standard half-strength MS medium, the seedlings were transferred onto half-strength MS medium plates containing different Mn2+ concentrations as specified in “Results.” The plates were then positioned in an inverted orientation for another few days before photographs were taken by scanning the plates using a Umax Astra 1200S scanner. Root measurement was conducted using ScionImage software (Scion). The wild-type and mutant plants were treated with the same conditions by placing them side by side on the same plate. Hydroponic Plant Growth for Extraction of Root AWF Arabidopsis seeds were dispersed on quarter-strength Hoagland medium (Hoagland and Arnon, 1950) solidified with 0.5% agar on the bottom of a 1-mL tip box (approximately 0.5 cm depth). After germination, the tip boxes were floated on quarter-strength Hoagland medium (pH 5.5, 10 mm MES-K) aerated by a fish tank air pump. Medium was replaced twice per week to prevent algal contamination. Roots penetrating the medium were excised after 3 to 4 weeks. DNA Manipulations cDNA Cloning and Molecular Constructs ECA3 cDNA was amplified by PCR from first-strand cDNA. The template was reverse transcribed from total RNA of 3-week-old rosette leaves using primers ECA3-f and ECA3-r (Supplemental Table S1). Proofreading High-Fidelity Taq DNA Polymerase Deep Vent (New England Biolabs) was used to amplify the DNA. The PCR product was purified by gel extraction and ligated to an EcoRV-linearized vector pBluescript SK+ (Stratagene). The cloned sequence was verified by sequencing (GenBank accession no. AY650902) and used for subsequent cDNA subcloning. AtECA Promoter∷GUS Constructs Genomic DNA was isolated from 4-week-old plants using the cetyl-trimethyl-ammonium bromide method (Ausubel et al., 1988). Based on the annotation of bacterial artificial chromosome clone T27I1 (AC004122), the region between the AtECA3 start codon and its immediate upstream ORF (AK230347) was taken as the ECA3 promoter. This region was amplified using primer sequences with appended restriction enzyme sites, ECA3-pf and ECA3-pr (Supplemental Table S1). The PCR-amplified product of 5.2 kb was digested with XhoI and NcoI and cloned into a GUS ORF-containing vector pRITA to make a promoter∷GUS construct, ECA3-RITA. The construct was verified by sequencing. The NotI-NotI fragment of ECA-RITA was ligated to the binary vector pMLBART. The resulting pECA3-GUS-MLBART construct was introduced into plants by the floral dip method (Clough and Bent, 1998), and plants homozygous for a Basta resistance marker were analyzed for promoter∷GUS activity. Transgenic plants containing ECA1 promoter∷GUS were obtained using a similar method. Primers ECA1-pf and ECA1-pr (Supplemental Table S1) were used to amplify a 3.1-kb fragment upstream of the ECA1 ORF. GFP-Tagged AtECA3 Conventional cloning and Gateway cloning methods were used to obtain GFP-tagged AtECA3. For conventional cloning, AtECA3 cDNA was amplified by PCR using platinum Pfx DNA polymerase (Invitrogen) and the primer pair ECA3-GFPf and ECA3-GFPr (Supplemental Table S1). The resultant PCR-amplified product for the C-tail-fused GFP was digested with BspHI and ligated to the NcoI-cut vector pAVA393 (von Arnim et al., 1998). The resultant construct, ECA3-GFP-393, was verified by sequencing of the AtECA3 coding region and contains a CaMV 35S promoter. For Gateway cloning, the AtECA3 cDNA was amplified by PCR using Platinum Pfx DNA polymerase (Invitrogen) and primers ECA3-Gf and ECA3-Gr. The PCR-amplified fragment of AtECA3 (stop codon removed) was cloned into the Gateway vector pDONR221 (Invitrogen) to produce an entry clone, ECA3-DONR221, using BP recombination cloning strategy. The sequence of the AtECA3 insert was verified. The clone ECA3-DONR221 was then cloned into the Gateway destination binary vector pK7FWG2 by LR recombination (Karimi et al., 2002). The resultant construct, ECA3-FWG, contains an expression cassette of CaMV P35S-ECA3-eGFP-T35S. Both conventional clones and Gateway clones were used in localization experiments. Agrobacterium-Mediated Plant Transformation and Histochemical GUS Staining Agrobacterium tumefaciens strain GV3101 was transformed with the binary vectors via electroporation and transformants were selected on Luria-Bertani plates with gentamicin and spectinomycin. Arabidopsis ecotype Col plants were transformed with Agrobacterium using the floral dip method (Clough and Bent, 1998). Plant transformants were selected on plates containing Basta (50 mg L−1 glufosinate ammonium [Crescent Chemical]) or 50 μg mL−1 kanamycin. At least five T3 lines were checked for a consistent GUS staining pattern (Lagarde et al., 1996). Samples at various stages were harvested in 90% acetone, rinsed once with staining buffer containing 50 mm Na+ phosphate (pH 7.2), 0.5 mM K4Fe[CN]6, and 0.5 mm K3Fe[CN]6, and then incubated for 48 h at 37°C in buffer containing 1 mm X-Gluc. The reaction was stopped in 70% ethanol, and chlorophyll was cleared in 95% ethanol. GUS activity was visualized with a Nikon Eclipse E600 microscope equipped with differential interference contrast (Nikon Instruments), and images were recorded using a Nikon DXM1200 digital camera. Yeast Strains, Plasmids, Transformation, and Growth The yeast (Saccharomyces cerevisiae) strains used were W303-1A (MATa, ade2-1 can1-100 his3-11,15 leu2-3,112 trp1-1 ura3-1), K616 (Pmr1∷HIS3 pmc1∷TRP1 cnb1∷LEU2), and K667 (cnb1∷LEU2 pmc1∷TRP vcx1Δ; Cunningham and Fink, 1994, 1996). Yeast was transformed with AtECA3 constructs by the lithium acetate method (Gietz et al., 1992). AtECA3 cDNA was initially subcloned into the yeast expression vector p426 (Mumberg et al., 1994) by ternary ligation of three fragments: 1.2-kb fragment of a KpnI/HindIII-digested ECA3-BSK clone, 1.6-kb fragment of a SpeI/KpnI-digested ECA3-BSK, and 6.3-kb fragment of a SpeI/HindIII-digested p426. This strategy was taken due to limited restriction enzyme sites in the p426 vector and an internal KpnI site in AtECA3. The final vector, p426-ECA3, contains a GAL1 promoter∷AtECA3 expression cassette and was verified by enzyme digestion. For Gateway cloning, ECA3-DONR221 was recombined with three destination vectors, pYES-DEST52 (Invitrogen), pYESDR196, and pGWFDR196 (Supplemental Materials and Methods S1). The first two cassettes drive strong expression of ECA3 under the GAL1 promoter (GAL1∷ECA3) and the PMA1 promoter (PMA1∷ECA3). In pYESDR196, the GAL1 promoter was replaced by the PMA1 promoter (Supplemental Materials and Methods S1). The pGWDR196 vector uses the PMA1 promoter to drive the expression of ECA3 fused at its C-terminal tail to GFP. At least three independent transformants from each construct were inoculated in synthetic complete medium with Glc but no uracil (SC-URA/glu). An overnight culture (5–10 mL) was diluted to an A 600 of 0.5, washed twice, and suspended in sterile water. A six-step serial dilution of 5-fold was prepared in sterile water for each culture. Five microliters of each was spotted onto the SC-URA plates (with Glc or Gal) supplemented with different ions or EGTA. The pH of the medium was maintained with 10 mm MES-KOH at pH 5.5 or 6.4. Growth at 30°C was recorded at varying times. Transient Expression in Arabidopsis Mesophyll Protoplast Protoplast Isolation Transient expression was conducted according to published protocols with modifications (Jin et al., 2001; Sheen, 2001; Uemura et al., 2004; Yoo et al., 2007). Arabidopsis leaves from approximately 3-week-old plants grown under continuous low light (40–50 μE m−2 s−1) and constant temperature (21°C) were cut into small strips and digested in 2.5 mL of enzyme solution for 3 h. The digestion solution consisted of 1.3% cellulose R10, 0.25% macerozyme R100 (Yakult), 0.4 m mannitol, 20 mm KCl, 20 mm MES at pH 5.7, 10 mm CaCl2, 0.1% fetal bovine serum (Sigma; no. F6178), and 2.5 mm β-mercaptoethanol. Protoplasts were filtered through 70-μm nylon mesh and centrifuged at 100g for 2 min. The pellets were washed twice in W5 solution containing 0.35 m mannitol, 125 mm CaCl2, 5 mm KCl, 5 mm Glc, and 2 mm MES at pH 5.7 by centrifugation at 100g for 1 min. Protoplasts were resuspended in MMg solution (0.4 m mannitol, 15 mm MgCl2, and 4 mm MES at pH 5.7) prior to transfection. Plasmids were purified by Miniprep kit (QIAGEN; no. 27160) or Plasmid Midi kit (QIAGEN; no. 12143) and resuspended in 0.4 m mannitol. For each transfection, 10 μL of protoplast suspension (1–2 × 104 cells) was added to a mixture of 40 μL of plasmids (5–10 μg per plasmid), 5 μL of M10Mg solution (0.4 m mannitol, 150 mm MgCl2, and 40 mm MES), and 55 μL of PEG-Ca solution (40% PEG4000 [Fluka; no. 81240], 0.2 m mannitol, and 100 mm CaNO3). After incubation at room temperature for 20 to 30 min, the transfection mixture was diluted with 700 μL of W5 solution and centrifuged at 100g for 45 s. After supernatant removal, protoplasts were resuspended in 300 μL of WI solution (0.5 m mannitol, 8 mm K2HPO4, and 2 mm MES) and 400 μL of MS solution (0.45 m mannitol, 1× MS salt mixture [GIBCO; no. 11117-058], 1× Gamborg's vitamin solution [Sigma; no. G1019], 2% Suc, 2 mm MES, and 100 μg/mL ampicillin). Transfected protoplasts were incubated in the dark at room temperature for 18 to 24 h before microscopy. In general, the efficiency of a single transfection of marker proteins is 50% or more; however, the efficiency is lower in cotransfections due to differences in fluorescent signals and the expression level of each gene. Confocal Microscopy Fluorescent signals in protoplasts were examined on the Zeiss LSM510 confocal microscope (Carl Zeiss), usually 18 to 24 h after transfection. The filter sets used for excitation (Ex) and emission (Em) are as follows: GFP, 488 nm (Ex)/BP505 to 530 nm (Em); RFP, 543 nm (Ex)/BP560 to 615 nm (Em); chlorophyll, 543 nm (Ex)/LP650 nm (Em); bright field, 633 nm. Signals were captured in multichannel mode. Images were analyzed and processed in the Zeiss LSM image browser (Carl Zeiss) and Adobe Photoshop (Adobe Systems). To examine yeast cells expressing GFP, liquid cultures grown overnight in SC-URA Glc medium with A 600 of 0.2 to 0.4 were used. Apoplastic Wall Fluid and Peroxidase Activity AWF was prepared from roots of Arabidopsis grown hydroponically in modified quarter-strength Hoagland medium (5 mm MES-K, pH 5.7; Hoagland and Arnon, 1950). The method was modified from that used to extract apoplastic wall fluid from leaves (Rathmell and Sequeira, 1974; Fecht-Christoffers et al., 2006). Arabidopsis roots (0.1–0.5 g fresh weight) were rinsed in DI water and then excised into 10 mm Na phosphate buffer (pH 6.0). Excised roots were submerged in 10 mL of buffer and subjected to vacuum infiltration (<−35 kPa) for 5 min. The roots were then carefully blotted dry on filter paper, weighed, and put into a 5-mL syringe barrel. The barrel was placed in a 15-mL Falcon tube, and the whole ensemble was centrifuged at 3,000g for 20 min. The AWF (approximately 30–200 μL) was collected from the bottom of the Falcon tube. The relative recovery of apoplastic fluid volume from wild-type (ecotype Col) or mutant tissue was similar when the fresh weight of the tissue was similar. Therefore, the fresh weight of mutant and wild-type tissue for each independent experiment was kept nearly equivalent. The total protein in the extracted AWF was estimated using a Bio-Rad protein assay dye reagent (Bradford, 1976). Peroxidase activity of the AWF fraction was determined from the rate of oxidation of guaiacol to tetraguaiacol (Maehly and Chance, 1954; Cordoba-Pedregosa et al., 1996). In the presence of peroxidases, the artificial substrate guaiacol (Kasei Kogyo) was oxidized by hydrogen peroxide to tetraguaiacol, which was monitored as an increase in A 470. Briefly, 10-, 20-, and 30-μL AWF samples containing 0.1 to 2 μg of total protein were added to a 1-mL reaction mixture containing 0.3% (v/v) hydrogen peroxide and 0.1% (v/v) guaiacol in 10 mm sodium phosphate at pH 6.0. The reaction was started by adding guaiacol, and the increase in A 470 was recorded for an initial 2 min using a Beckman DU 640 spectrophotometer at room temperature. The rate of A 470 change was expressed as nanomoles per minute per gram of tissue (fresh weight) using a molecular extinction coefficient of 26.6 mm −1 cm−1. At least three independent experiments were conducted for each set of wild-type and mutant plants. Sequence data from this article can be found in the GenBank/EMBL data libraries under accession number AY650902. Supplemental Data The following materials are available in the online version of this article. Supplemental Figure S1. Full alignment of ECAs and SERCAs. Supplemental Figure S2. Localization of AtECA3-GFP in yeast. Supplemental Figure S3. AtECA1 promoter∷GUS activity. Supplemental Figure S4. Root map expression of AtECA1, ECA2, and ECA3. Supplemental Table S1. Primers used. Supplemental Materials and Methods S1. Gateway vectors for expression in yeast. ACKNOWLEDGMENTS We are grateful to Walter J. Horst and Hendrik Führs (University of Hanover) for advice on APX assays and Inhwan Hwang (Pohang University) for advice on transient expression in protoplasts. Fluorescence-tagged markers were gifts from T. Ueda (University of Tokyo), Inhwan Hwang, J.F. Harper (University of Nevada), J.Y. Lee (University of Delaware), and A. Nebenfuhr (University of Tennessee). We thank Anke Reinders and John M. Ward (University of Minnesota), K.D. Hirschi (Baylor College of Medicine), and Rajini Rao (Johns Hopkins University) for advice and valuable suggestions. Technical assistance was provided in part by Kevin W. Bock and Hong Zhao. LITERATURE CITED Alonso JM, Stepanova AN, Leisse TJ, Kim CJ, Chen H, Shinn P, Stevenson DK, Zimmerman J, Barajas P, Cheuk R, et al ( 2003 ) Genome-wide insertional mutagenesis of Arabidopsis thaliana. Science 301 : 653 – 657 Crossref Search ADS PubMed Ausubel FM, Brent R, Kingston RE, Moore D, Seidman JG, Smith JA, Struhl K ( 1988 ) Current Protocols in Molecular Biology. Greene Publishing Associates and Wiley-Interscience, New York Battey NH, Blackbourn HD ( 1993 ) The control of exocytosis in plant cells. New Phytol 125 : 307 – 338 Crossref Search ADS PubMed Battey NH, James NC, Greenland AJ, Brownlee C ( 1999 ) Exocytosis and endocytosis. Plant Cell 11 : 643 – 660 Crossref Search ADS PubMed Baxter I, Tchieu J, Sussman MR, Boutry M, Palmgren MG, Gribskov M, Harper JF, Axelsen KB ( 2003 ) Genomic comparison of P-type ATPase ion pumps in Arabidopsis and rice. Plant Physiol 132 : 618 – 628 Crossref Search ADS PubMed Bonza MC, Morandini P, Luoni L, Geisler M, Palmgren MG, De Michelis MI ( 2000 ) At-ACA8 encodes a plasma membrane-localized calcium-ATPase of Arabidopsis with a calmodulin-binding domain at the N terminus. Plant Physiol 123 : 1495 – 1506 Crossref Search ADS PubMed Bradford MM ( 1976 ) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72 : 248 – 254 Crossref Search ADS PubMed Brandizzi F, Hawes C ( 2004 ) A long and winding road: symposium on membrane trafficking in plants. EMBO Rep 5 : 245 – 249 Crossref Search ADS PubMed Carpita N, McCann M ( 2000 ) The cell wall. In BB Buchanan, W Gruissem, RL Jones, eds, Biochemistry and Molecular Biology of Plants. American Society of Plant Physiologists, Rockville, MD, pp 52–108 Clough SJ, Bent AF ( 1998 ) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16 : 735 – 743 Crossref Search ADS PubMed Cordoba-Pedregosa M, Gonzalez-Reyes JA, Canadillas M, Navas P, Cordoba F ( 1996 ) Role of apoplastic and cell-wall peroxidases on the stimulation of root elongation by ascorbate. Plant Physiol 112 : 1119 – 1125 Crossref Search ADS PubMed Cunningham K, Fink G ( 1994 ) Calcineurin-dependent growth control in Saccharomyces cerevisiae mutants lacking PMC1, a homolog of plasma membrane Ca2+ ATPases. J Cell Biol 124 : 351 – 363 Crossref Search ADS PubMed Cunningham K, Fink G ( 1996 ) Calcineurin inhibits VCX1-dependent H+/Ca2+ exchange and induces Ca2+ ATPases in Saccharomyces cerevisiae. Mol Cell Biol 16 : 2226 – 2237 Crossref Search ADS PubMed Dauwalder M, Roux SJ, Rabenberg LK ( 1985 ) Cellular and subcellular localization of calcium in gravistimulated corn roots. Protoplasma 129 : 137 – 148 Crossref Search ADS PubMed Durr G, Strayle J, Plemper R, Elbs S, Klee SK, Catty P, Wolf DH, Rudolph HK ( 1998 ) The medial-Golgi ion pump Pmr1 supplies the yeast secretory pathway with Ca2+ and Mn2+ required for glycosylation, sorting, and endoplasmic reticulum-associated protein degradation. Mol Biol Cell 9 : 1149 – 1162 Crossref Search ADS PubMed Fecht-Christoffers MM, Fuhrs H, Braun HP, Horst WJ ( 2006 ) The role of hydrogen peroxide-producing and hydrogen peroxide-consuming peroxidases in the leaf apoplast of cowpea in manganese tolerance. Plant Physiol 140 : 1451 – 1463 Crossref Search ADS PubMed Geisler M, Frangne N, Gomes E, Martinoia E, Palmgren MG ( 2000 ) The ACA4 gene of Arabidopsis encodes a vacuolar membrane calcium pump that improves salt tolerance in yeast. Plant Physiol 124 : 1814 – 1827 Crossref Search ADS PubMed Geldner N ( 2004 ) The plant endosomal system: its structure and role in signal transduction and plant development. Planta 219 : 547 – 560 PubMed Gietz D, St Jean A, Woods RA, Schiestl RH ( 1992 ) Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Res 20 : 1425 Crossref Search ADS PubMed Gouet P, Courcelle E, Stuart DI, Metoz F ( 1999 ) ESPript: analysis of multiple sequence alignments in PostScript. Bioinformatics 15 : 305 – 308 Crossref Search ADS PubMed Harper JF, Hong B, Hwang I, Guo HQ, Stoddard R, Huang JF, Palmgren MG, Sze H ( 1998 ) A novel calmodulin-regulated Ca2+-ATPase (ACA2) from Arabidopsis with an N-terminal autoinhibitory domain. J Biol Chem 273 : 1099 – 1106 Crossref Search ADS PubMed Hepler PK, Vidali L, Cheung AY ( 2001 ) Polarized cell growth in higher plants. Annu Rev Cell Dev Biol 17 : 159 – 187 Crossref Search ADS PubMed Hoagland DR, Arnon DI ( 1950 ) The water-culture for growing plants without soil. Univ Calif Coll Agric Exp Stn Circ 347 Homann U, Tester M ( 1997 ) Ca2+-independent and Ca2+/GTP-binding protein-controlled exocytosis in a plant cell. Proc Natl Acad Sci USA 94 : 6565 – 6570 Crossref Search ADS PubMed Huh WK, Falvo JV, Gerke LC, Carroll AS, Howson RW, Weissman JS, O'Shea EK ( 2003 ) Global analysis of protein localization in budding yeast. Nature 425 : 686 – 691 Crossref Search ADS PubMed Jin JB, Kim YA, Kim SJ, Lee SH, Kim DH, Cheong GW, Hwang I ( 2001 ) A new dynamin-like protein, ADL6, is involved in trafficking from the trans-Golgi network to the central vacuole in Arabidopsis. Plant Cell 13 : 1511 – 1526 Crossref Search ADS PubMed Karimi M, Inze D, Depicker A ( 2002 ) GATEWAY(TM) vectors for Agrobacterium-mediated plant transformation. Trends Plant Sci 7 : 193 – 195 Crossref Search ADS PubMed Kim DH, Eu YJ, Yoo CM, Kim YW, Pih KT, Jin JB, Kim SJ, Stenmark H, Hwang I ( 2001 ) Trafficking of phosphatidylinositol 3-phosphate from the trans-Golgi network to the lumen of the central vacuole in plant cells. Plant Cell 13 : 287 – 301 Crossref Search ADS PubMed Lagarde D, Basset M, Lepetit M, Conejero G, Gaymard F, Astruc S, Grignon C ( 1996 ) Tissue-specific expression of Arabidopsis AKT1 gene is consistent with a role in K+ nutrition. Plant J 9 : 195 – 203 Crossref Search ADS PubMed Lee GJ, Sohn EJ, Lee MH, Hwang I ( 2004 ) The Arabidopsis rab5 homologs rha1 and ara7 localize to the prevacuolar compartment. Plant Cell Physiol 45 : 1211 – 1220 Crossref Search ADS PubMed Li X ( 2006 ) The importance of sorting calcium in plant cells: uncovering the roles of a SERCA-like Ca-ATPase. PhD thesis. University of Maryland, College Park, MD Liang F, Cunningham KW, Harper JF, Sze H ( 1997 ) ECA1 complements yeast mutants defective in Ca2+ pumps and encodes an endoplasmic reticulum-type Ca2+-ATPase in Arabidopsis thaliana. Proc Natl Acad Sci USA 94 : 8579 – 8584 Crossref Search ADS PubMed Liang F, Sze H ( 1998 ) A high-affinity Ca2+ pump, ECA1, from the endoplasmic reticulum is inhibited by cyclopiazonic acid but not by thapsigargin. Plant Physiol 118 : 817 – 825 Crossref Search ADS PubMed Maehly A, Chance B ( 1954 ) The assay of catalases and peroxidases. Methods Biochem Anal 1 : 357 – 424 PubMed Marschner H ( 1995 ) Mineral Nutrition of Higher Plants, Ed 2. Academic Press, London McElver J, Tzafrir I, Aux G, Rogers R, Ashby C, Smith K, Thomas C, Schetter A, Zhou Q, Cushman MA, et al ( 2001 ) Insertional mutagenesis of genes required for seed development in Arabidopsis thaliana. Genetics 159 : 1751 – 1763 Crossref Search ADS PubMed Mills RF, Doherty ML, Lopez-Marques RL, Weimar T, Dupree P, Palmgren MG, Pittman JK, Williams LE ( 2008 ) ECA3, a Golgi-localized P2A-type ATPase, plays a crucial role in manganese nutrition in Arabidopsis. Plant Physiol 146 : 116 – 128 Crossref Search ADS PubMed Mumberg D, Muller R, Funk M ( 1994 ) Regulatable promoters of Saccharomyces cerevisiae: comparison of transcriptional activity and their use for heterologous expression. Nucleic Acids Res 22 : 5767 – 5768 Crossref Search ADS PubMed Murashige T, Skoog F ( 1962 ) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15 : 473 – 497 Crossref Search ADS Nebenfuhr A, Staehelin LA ( 2001 ) Mobile factories: Golgi dynamics in plant cells. Trends Plant Sci 6 : 160 – 167 Crossref Search ADS PubMed Ordenes VR, Reyes FC, Wolff D, Orellana A ( 2002 ) A thapsigargin-sensitive Ca2+ pump is present in the pea Golgi apparatus membrane. Plant Physiol 129 : 1820 – 1828 Crossref Search ADS PubMed Passardi F, Cosio C, Penel C, Dunand C ( 2005 ) Peroxidases have more functions than a Swiss army knife. Plant Cell Rep 24 : 255 – 265 Crossref Search ADS PubMed Pittman JK, Mills RF, O'Connor CD, Williams LE ( 1999 ) Two additional type IIA Ca(2+)-ATPases are expressed in Arabidopsis thaliana: evidence that type IIA sub-groups exist. Gene 236 : 137 – 147 Crossref Search ADS PubMed Portzehl H, Caldwell PC, Rueegg JC ( 1964 ) The dependence of contraction and relaxation of muscle fibres from the crab Maia squinado on the internal concentration of free calcium ions. Biochim Biophys Acta 79 : 581 – 591 PubMed Rathmell WG, Sequeira L ( 1974 ) Soluble peroxidase in fluid from the intercellular spaces of tobacco leaves. Plant Physiol 53 : 317 – 318 Crossref Search ADS PubMed Rentsch D, Laloi M, Rouhara I, Schmelzer E, Delrot S, Frommer WB ( 1995 ) NTR1 encodes a high affinity oligopeptide transporter in Arabidopsis. FEBS Lett 370 : 264 – 268 Crossref Search ADS PubMed Rizzuto R, Pozzan T ( 2006 ) Microdomains of intracellular Ca2+: molecular determinants and functional consequences. Physiol Rev 86 : 369 – 408 Crossref Search ADS PubMed Robinson DG ( 2003 ) The Golgi Apparatus and the Plant Secretory Pathway. Blackwell/CRC Press, Oxford/Boca Raton, FL Rudolph HK, Antebi A, Fink GR, Buckley CM, Dorman TE, LeVitre J, Davidow LS, Mao JI, Moir DT ( 1989 ) The yeast secretory pathway is perturbed by mutations in PMR1, a member of a Ca2+ ATPase family. Cell 58 : 133 – 145 Crossref Search ADS PubMed Sakai-Wada A, Yagi S ( 1993 ) Ultrastructural studies on the Ca2+ localization in the dividing cells of the maize root tip. Cell Struct Funct 18 : 389 – 397 Crossref Search ADS PubMed Samaj J, Read ND, Volkmann D, Menzel D, Baluska F ( 2005 ) The endocytic network in plants. Trends Cell Biol 15 : 425 – 433 Crossref Search ADS PubMed Sanders D, Brownlee C, Harper JF ( 1999 ) Communicating with calcium. Plant Cell 11 : 691 – 706 Crossref Search ADS PubMed Schiott M, Romanowsky SM, Baekgaard L, Jakobsen MK, Palmgren MG, Harper JF ( 2004 ) A plant plasma membrane Ca2+ pump is required for normal pollen tube growth and fertilization. Proc Natl Acad Sci USA 101 : 9502 – 9507 Crossref Search ADS PubMed Sheen J ( 2001 ) Signal transduction in maize and Arabidopsis mesophyll protoplasts. Plant Physiol 127 : 1466 – 1475 Crossref Search ADS PubMed Shimada T, Fuji K, Tamura K, Kondo M, Nishimura M, Hara-Nishimura I ( 2003 ) Vacuolar sorting receptor for seed storage proteins in Arabidopsis thaliana. Proc Natl Acad Sci USA 100 : 16095 – 16100 Crossref Search ADS PubMed Smith RA, Duncan MJ, Moir DT ( 1985 ) Heterologous protein secretion from yeast. Science 229 : 1219 – 1224 Crossref Search ADS PubMed Steer MW ( 1988 ) The role of calcium in exocytosis and endocytosis in plant cells. Physiol Plant 72 : 213 – 220 Crossref Search ADS Sze H, Liang F, Hwang I, Curran AC, Harper JF ( 2000 ) Diversity and regulation of plant Ca2+ pumps: insights from expression in yeast. Annu Rev Plant Physiol Plant Mol Biol 51 : 433 – 462 Crossref Search ADS PubMed Ton VK, Mandal D, Vahadji C, Rao R ( 2002 ) Functional expression in yeast of the human secretory pathway Ca(2+),Mn(2+)-ATPase defective in Hailey-Hailey disease. J Biol Chem 277 : 6422 – 6427 Crossref Search ADS PubMed Ton VK, Rao R ( 2004 ) Functional expression of heterologous proteins in yeast: insights into Ca2+ signaling and Ca2+-transporting ATPases. Am J Physiol Cell Physiol 287 : C580 – 589 Crossref Search ADS PubMed Toyoshima C, Nomura H ( 2002 ) Structural changes in the calcium pump accompanying the dissociation of calcium. Nature 418 : 605 – 611 Crossref Search ADS PubMed Ueda T, Uemura T, Sato MH, Nakano A ( 2004 ) Functional differentiation of endosomes in Arabidopsis cells. Plant J 40 : 783 – 789 Crossref Search ADS PubMed Ueda T, Yamaguchi M, Uchimiya H, Nakano A ( 2001 ) Ara6, a plant-unique novel type Rab GTPase, functions in the endocytic pathway of Arabidopsis thaliana. EMBO J 20 : 4730 – 4741 Crossref Search ADS PubMed Uemura T, Ueda T, Ohniwa RL, Nakano A, Takeyasu K, Sato MH ( 2004 ) Systematic analysis of SNARE molecules in Arabidopsis: dissection of the post-Golgi network in plant cells. Cell Struct Funct 29 : 49 – 65 Crossref Search ADS PubMed Van Baelen K, Dode L, Vanoevelen J, Callewaert G, De Smedt H, Missiaen L, Parys JB, Raeymaekers L, Wuytack F ( 2004 ) The Ca2+/Mn2+ pumps in the Golgi apparatus. Biochim Biophys Acta 1742 : 103 – 112 Crossref Search ADS PubMed von Arnim AG, Deng XW, Stacey MG ( 1998 ) Cloning vectors for the expression of green fluorescent protein fusion proteins in transgenic plants. Gene 221 : 35 – 43 Crossref Search ADS PubMed Watanabe E, Shimada T, Kuroyanagi M, Nishimura M, Hara-Nishimura I ( 2002 ) Calcium-mediated association of a putative vacuolar sorting receptor PV72 with a propeptide of 2S albumin. J Biol Chem 277 : 8708 – 8715 Crossref Search ADS PubMed Wu Z, Liang F, Hong B, Young JC, Sussman MR, Harper JF, Sze H ( 2002 ) An endoplasmic reticulum-bound Ca2+/Mn2+ pump, ECA1, supports plant growth and confers tolerance to Mn2+ stress. Plant Physiol 130 : 128 – 137 Crossref Search ADS PubMed Wuytack F, Raeymaekers L, Missiaen L ( 2003 ) PMR1/SPCA Ca2+ pumps and the role of the Golgi apparatus as a Ca2+ store. Pflugers Arch 446 : 148 – 153 Crossref Search ADS PubMed Yoo SD, Cho YH, Sheen J ( 2007 ) Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis. Nat Protocols 2 : 1565 – 1572 Crossref Search ADS PubMed Author notes 1 This work was supported by the Maryland Agricultural Experiment Station, the Department of Energy (grant nos. DE–FG02–95ER20200 and DE–FG02–07ER15883 to H.S. and grant no. DE–FG03–94ER20152 to J.F.H.), and the National Institutes of Health (grant no. 1RO1 GM–070813–01 to J.F.H.). S.C. was supported by a Science and Technology Graduate Fellowship from the Royal Thai Government. 2 Present address: Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520. 3 Present address: Beijing Research Center of Agro-Biotechnology, Beijing 100089, China. * Corresponding author; e-mail hsze@umd.edu. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Heven Sze (hsze@umd.edu). [C] Some figures in this article are displayed in color online but in black and white in the print edition. [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.108.119909 © 2008 American Society of Plant Biologists © The Author(s) 2008. Published by Oxford University Press on behalf of American Society of Plant Biologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
TI - A Distinct Endosomal Ca2+/Mn2+ Pump Affects Root Growth through the Secretory Process      
JF - Plant Physiology
DO - 10.1104/pp.108.119909
DA - 2008-08-04
UR - https://www.deepdyve.com/lp/oxford-university-press/a-distinct-endosomal-ca2-mn2-pump-affects-root-growth-through-the-eLq2XCCtzo
SP - 1675
EP - 1689
VL - 147
IS - 4
DP - DeepDyve
ER -