Characterization of a putative grapevine Zn transporter, VvZIP3, suggests its involvement in early reproductive development in Vitis vinifera L
© Gainza-Cortés et al.; licensee BioMed Central Ltd. 2012
Received: 10 March 2012
Accepted: 29 June 2012
Published: 23 July 2012
Zinc (Zn) deficiency is one of the most widespread mineral nutritional problems that affect normal development in plants. Because Zn cannot passively diffuse across cell membranes, it must be transported into intracellular compartments for all biological processes where Zn is required. Several members of the Zinc-regulated transporters, Iron-regulated transporter-like Protein (ZIP) gene family have been characterized in plants, and have shown to be involved in metal uptake and transport. This study describes the first putative Zn transporter in grapevine. Unravelling its function may explain an important symptom of Zn deficiency in grapevines, which is the production of clusters with fewer and usually smaller berries than normal.
We identified and characterized a putative Zn transporter from berries of Vitis vinifera L., named VvZIP3. Compared to other members of the ZIP family identified in the Vitis vinifera L. genome, VvZIP3 is mainly expressed in reproductive tissue - specifically in developing flowers - which correlates with the high Zn accumulation in these organs. Contrary to this, the low expression of VvZIP3 in parthenocarpic berries shows a relationship with the lower Zn accumulation in this tissue than in normal seeded berries where its expression is induced by Zn. The predicted protein sequence indicates strong similarity with several members of the ZIP family from Arabidopsis thaliana and other species. Moreover, VvZIP3 complemented the growth defect of a yeast Zn-uptake mutant, ZHY3, and is localized in the plasma membrane of plant cells, suggesting that VvZIP3 has the function of a Zn uptake transporter.
Our results suggest that VvZIP3 encodes a putative plasma membrane Zn transporter protein member of the ZIP gene family that might play a role in Zn uptake and distribution during the early reproductive development in Vitis vinifera L., indicating that the availability of this micronutrient may be relevant for reproductive development.
Zinc is an essential micronutrient that plays many important roles in various physiological and metabolic processes in all living organisms. It functions as a cofactor for over 300 enzymes and proteins involved in cell division, nucleic acid metabolism and protein synthesis, and is critical in the control of gene transcription and the coordination of other biological processes regulated by proteins containing DNA-binding Zn-finger motifs, RING fingers and LIM domains [1–4].
It has been demonstrated that Zn deficiency is one of the most widespread mineral nutritional problems affecting normal development in plants [5–8]. This includes altered expression and/or function of proteins at the metabolic level that leads to different physiological symptoms characterized by root apex necrosis. At the same time, sub-lethal Zn deficiency induces spatial heterogeneous or interveinal chlorosis, development of reddish-brown or bronze tints and a range of auxin deficiency-like responses such as internode shortening, epinasty, inward curling of leaf lamina and reduction of leaf size [4–9]. In grapevines, deficit of Zn results in the development of leaves that are smaller than normal and/or mottled, and shortened internodes. It has been suggested that this reduction in shoot growth results from the fact that Zn is essential for the synthesis of tryptophan, a precursor of the phytohormone indoleacetic acid (IAA) . Another important symptom of Zn deficiency in grapevines is the production of clusters with few berries that also vary in size from normal to very small [10–12]. In this way, vineyards commonly correct Zn deficiency with both soil and foliar application of fertilizers. Under conditions of Zn deficiency, application of foliar Zn fertilizer shortly before anthesis increases the number of flowers that set fruit [10–14].
Since Zn cannot passively diffuse across cell membranes, it must be transported into intracellular compartments for all biological processes where Zn is required. Several members of the 15 Zinc-regulated transporters, Iron-regulated transporter-like Protein (ZIP) gene family have been characterized in Arabidopsis thaliana, and their involvement in metal uptake and transport in plants has been demonstrated [16–18].
Arabidopsis ZIP1 and ZIP3 genes are expressed in roots in response to Zn deficiency, suggesting that they transport Zn from the soil to the plant. ZIP4 is expressed either in roots and shoots, showing a delicate regulation to control the homeostasis of Zn, thus avoiding potential toxic effects of this micronutrient [15, 17]. Additionally, these three transporters restore Zn uptake in the yeast Zn-uptake mutant, Δzrt1/Δzrt2 (ZHY3 strain), confirming its implication in Zn homeostasis [15, 19–22]. Moreover, ZIP2 and ZIP4 can rescue yeast mutants deficient in copper (Cu) transport, and ZIP4 is up-regulated in Cu-deficient roots . Although several ZIP genes have been identified and functionally characterized at the molecular level [2, 24], the complete gene family and their role in metal homeostasis is not fully understood. In this way, a considerably large family of ZIP genes has been currently characterized from various species, such as Thlaspi japonicum, Thlaspi caerulescens[17, 26–28], soybean , Medicago truncatula[30, 31] and rice [2, 24, 32, 33]. The availability of the full-genome sequence of grapevine (http://www.genoscope.cns.fr/spip/Vitis-vinifera-e.html) provides the opportunity to investigate the Zn homeostasis and their importance for the reproductive development in this organism. 20 ZIP genes have been identified recently in Vitis vinifera, but none of them has been functionally characterized.
Here, we report the isolation of VvZIP3, a member of the ZIP gene family from Vitis vinifera L. cv. Carménère, which encodes a Zn uptake protein. This gene was isolated from an expression library of Carménère berries and is highly homologous to AtZIP1 gene from Arabidopsis thaliana. Expression of VvZIP3 in the yeast Zn-uptake deficient mutant ZHY3 complemented its growth defect, indicating that VvZIP3 has the function of a putative Zn transporter. Moreover, the expression of the VvZIP3-mGFP5 fusion protein in onion epidermal cells indicated that is located at the plasma membrane. Expression analysis revealed that VvZIP3 was transcribed principally in reproductive tissues - specifically in developing flowers -, organs that also present the highest accumulation of Zn. These results suggest that VvZIP3 participates in Zn uptake during flower development contributing to the normal development in Vitis vinifera L.
VvZIP3 is a member of a Zn transporter encoding gene family
VvZIP3 is differentially expressed during grapevine development
VvZIP3 protein has conserved motifs associated to Zn transporters
VvZIP3 restores Zn-limited growth in the yeast ZHY3 double mutant strain
VvZIP3 is mainly expressed in the pericarp and skin of berries and is related to normal fruit development
In field conditions, Zn deficiency is commonly associated to the production of clusters with few berries that vary in size from normal seeded to very small or parthenocarpic unseeded berries, a viticulture problem known as millerandage[10–12]. In order to test whether VvZIP3 expression is being affected in such phenotype, its transcriptional profile was compared in normal and parthenocarpic grapes in an early developmental stage (pre-veraison) from three different seasons (S1, S2 and S3). This analysis revealed that expression of VvZIP3 was consistently repressed in parthenocarpic green berries compared to normal berries in the three growing seasons analyzed (Figure 6B). Taken together, these results suggest that VvZIP3 is mainly expressed when the plant needs high requirement of Zn (flowering and fruit setting) and that its expression is associated with the physiological processes that affect the normal berry development in grapevine.
Zn accumulation in reproductive tissue of Vitis vinifera L. cv. Carménère is associated to VvZIP3 expression profiles
The expression of VvZIP3 is induced by Zn in normal berries
Although several ZIP genes have been characterized in plants [15, 23, 37–40], to date, no ZIP gene has been isolated for Vitis species. The ZIP family of metal transporters shares several characteristics, including a molecular size between 36 and 39 kDa, 8 trans-membrane domains, a cytoplasmic ‘variable region’ localized between transmembrane domains 3 and 4 that provides a potential metal-binding domain and carboxy and amino termini located on the outer side of the targeted membrane [15, 21, 22]. Indeed, VvZIP3 displays all these structural characteristics allowing to be considered as a member of the ZIP family (Figure 3).
As shown in the phylogenetic tree (Figure 1), the predicted amino acid sequence of VvZIP3 was most closely related to AtZIP1, AtZIP3 and AtZIP5 (50–56% of identity) from A. thaliana[15, 16, 22] indicating that VvZIP3 and those proteins share, probably, a common evolutionary ancestor. All of these proteins are able to complement the growth of the yeast strain ZHY3. This yeast mutant type is very sensitive to Zn deprivation because of the mutation of their both high (ZRT1)- and low (ZRT2)-affinity Zn uptake systems [19, 20]. Similar to the Arabidopsis ZIP proteins, the grape ZIP protein encoded by the cDNA of VvZIP3 complemented the growth of this yeast mutant (Figure 5). Moreover, VvZIP3 was localized to the plasma membrane, as shown by the WOLF-pSORT II prediction and transient expression of a VvZIP3-mGFP5 fusion protein in onion epidermal cells (Figure 4A and 4B). Hence, these findings demonstrate that VvZIP3 gene encodes a putative Zn transporter that may participate in the uptake of this element in Vitis vinifera L..
The tissue-specific expression determined for grapevine ZIP encoding genes reflects the complexity of this gene family and suggests a differential gene regulation associated to the nutritional requirements of grapevine. In this regard, several ZIP genes identified in other species display diverse transcriptional profiles regarding tissue specificity and response to Zn status. For example, in rice, OsZIP4 mRNA accumulates in the phloem cells of the stem as well as in the vascular bundles of the roots and leaves [2, 32], OsZIP1 mRNA accumulates in Zn-deficient roots and shoots while OsZIP2 mRNA accumulates primarily in Zn-deficient roots . In the model legume Medicago truncatula MtZIP1 transcripts were only detected in Zn-deficient roots and leaves , while MtZIP2 gene was expressed in roots and stems, but not in leaves, and its transcriptional activity could be induced by Zn . In addition, the VvZIP3 counterparts identified in Arabidopsis (principally AtZIP1 AtZIP3 and AtZIP5) show a strong transcriptional activity in root tissue under Zn deficiency [15, 22]. Compared to other VvZIP genes (i.e VvZIP5.1), VvZIP3 is mainly transcribed in grapevine reproductive tissues under field conditions, more specifically in developing flowers and in the pericarp and/or skin of berries at early growth stages (Figure 2 and 6A). In these tissues, VvZIP3 expression seems to be induced in response to Zn exposure as deduced from the experiments with normal berries at pre-veraison stage under exogenous Zn treatment (Figure 8).
In addition, and even when VvZIP3 is not expressed in seeds, its transcriptional activity was consistently repressed in parthenocarpic non-seeded berries (Figure 6B). This down-regulation is not due to a non-specific disruptive effect on gene expression caused by seedlessness. When non-seeded/seeded expression ratio was determined for several transporter encoding genes both, up-regulated and down-regulated genes were identified (See Additional file 1). Interestingly, such analysis revealed that a gene coding for a putative grapevine boron transporter also appears strongly repressed in non-seeded berries. Like Zn, boron is also an essential micronutrient required for normal reproductive development in plants, and B deficiency has been associated to parthenocarpic berry development in grapevines [10, 41]. Similar to VvZIP3 VvBOR1 is predominantly expressed in flowers at anthesis and normal berries at early growth stages, preceding a B accumulation in reproductive tissues . This expression profile seems adequate to fulfill the B requirement for cross-linking of rhamnogalacturonane II, a polysaccharide essential for cell wall formation during pollen tube growth .
In a similar way, the VvZIP3 expression profile, its straight correlation with the Zn accumulation pattern during development of reproductive organs (Figure 7), and it’s up-regulation in response to an increase in vascular Zn content (Figure 8), suggests a participation of VvZIP3 in the Zn loading during early reproductive developmental stages. It has been reported that alteration of the expression of ZIP transporters affects Zn distribution. Recently, it has been demonstrated that constitutive over-expression of the OsZIP4 gene in transgenic rice plants confers disarrangement of Zn distribution in the transgenic plants . In these regard, we can speculate that the alteration of VvZIP3 expression during flowering and fertilization can modify the distribution, remobilization and availability of Zn, and hence affects normal reproductive development. Considering that Zn is essential for the stabilization of many proteins involved in development such as proteins containing DNA-binding Zn-finger motifs, RING fingers and LIM domains [1, 7, 10] and that Zn-finger transcription factors have been involved in the development and function of floral tissues such as anthers, tapetum, pollen and pistil secretory tissues in several plant species [1, 7, 44, 45], it is plausible to propose that VvZIP3 may play a key role in both flower and normal fruit development.
Considering that Zn deficiency produces several developmental problems in grapevines [10–12] and that no information is available regarding the specificity, regulation and function of any ZIP gene in Vitis vinifera L., this work provides relevant information about the functional characterization of a putative Zn transporter identified in this species. Using a functional molecular approach, our results suggest that VvZIP3 encodes a plasma membrane putative Zn transporter protein member of the ZIP gene family. VvZIP3 is principally expressed in reproductive tissues, being strongly repressed in parthenocarpic seedless berries that present lower zinc accumulation, suggesting that it may participate in Zn uploading for normal berry development and that changes in its expression could affect zinc availability during this process.
Grapevine (Vitis vinifera L. var. Carménère) grown under field conditions in a commercial vineyard in the Maule Valley (Central Chile) during three growing seasons (S1, S2 and S3) were used in this study. Zn nutritional status in plant leaves was monitored and corrected by foliar spray applications to maintain a Zn-sufficiency condition equivalent to a foliar concentration of 45–55 ppm. Random sampling of different organs was performed starting at early flowering until mature fruit stage (from October to April) from plants grown in the same plot. Stages to be sampled were defined according to the Modified Eichhorn-Lorenz System . Flowering stages collected were: EL19, inflorescences or little clusters (LC) and EL 23, flowers at full bloom (F). Fruit developmental stages were: EL31, berries at preveraison 7 mm in diameter (PV); EL35, berries at veraison (V) and EL38, berries at postveraison harvest-ripe (M). For sampling, phenological stages were determined for normal seeded berries, then clusters were collected and seeded and non-seeded berries from the some bunch were separated for further processing.
Identification and isolation of VvZIP3
From expression libraries made from RNA of normal and parthenocarpic Vitis vinifera L. cv. carménère berries (DEGECHIVID database; http://www.genomicafrutos.cl), an EST sequence highly similar to genes encoding Zn transporter proteins was obtained after comparison in the grapevine GENOSCOPE (http://www.genoscope.cns.fr/externe/GenomeBrowser/Vitis/) and NCBI (http://www.ncbi.nlm.nih.gov/genome/seq/BlastGen/BlastGen.cgi?taxid=29760) databases.
The sequence, named VvZIP3, was translated to obtain the open reading frame containing the initial methionine and the first stop codon using the OMIGA 2.0 software Vitis vinifera L.. Identification of conserved domains in the predicted protein was carried out using InterProScan (Hunter, et al. 2009) and ScanProsite (de Castro, et al. 2006). Grand average hydropathy was obtained according to Kyte and Doolittle model . Potential transmembrane domains in the predicted protein sequence were identified using TMPred , and TMHMM . Signal peptides, as well as possible subcellular targeting sites were assessed using Wolf PSORT-II software . Alignments were performed using ClustalW  and phylogenetic analyses were conducted with MEGA4 . Phylogenetic trees were inferred using the Neighbor-Joining method . The ZIP genes accession numbers used in tree construction are: Vitis vinifera (VvZIP1.1, GSVIVT00002087001; VvZIP1.2, GSVIVT00002088001; VvZIP2,GSVIVT00024285001; VvZIP3, GSVIVT00030117001; VvZIP4,GSVIVT00032208001; VvZIP5.1, GSVIVT00037538001; VvZIP5.2,GSVIVT00037540001; VvZIP6.1, GSVIVT00024060001; VvZIP6.2, GSVIVT00029326001; VvZIP7.1, GSVIVT00027686001; VvZIP7.2,GSVIVT00031911001; VvZIP8, GSVIVT00030650001; VvZIP9,GSVIVT00024638001; VvZIP10, GSVIVT00031915001; VvZIP11.1,GSVIVT00033348001; VvZIP11.2, GSVIVT00033353001; VvZIP11.3,GSVIVT00033352001; VvZIP11.4, GSVIVT00033350001; VvZIP12, GSVIVT00030116001; VvZIP13, GSVIVT00033649001) and Arabidopsis thaliana (AtZIP1, AT3G12750; AtZIP2, AT5G59520; AtZIP3, AT2G32270; AtZIP4, AT1G10970; AtZIP5, AT1G05300; AtZIP6, AT2G30080; AtZIP7, AT2G04032; AtZIP8, AT5G45105; AtZIP9, AT4G33020; AtZIP10, AT1G31260; AtZIP11, AT1G55910; AtZIP12, AT5G62160; AtZIP13, AT3G08650; AtIRT1, AT4G19690; AtIRT2, AT4G19680; AtIRT3, AT1G60960; AtIAR1, AT1G68100; AtGUFA, AT3G20870).
Plant RNA extraction
Total RNA was extracted from 2 to 3 g of frozen (−80°C) roots, leaves, stems, little clusters, flowers, fruits and seeds (from pre-veraison to mature grapes) using the modified CTAB method . Total RNA integrity was corroborated by formaldehyde agarose gel electrophoresis and their purity by OD260/280 ratio >1.95. Following DNase (DNAse I, Ambion) treatment of total RNA, first-strand cDNA synthesis was carried out from 2 μg of total RNA for each sample using oligo (dT) according to the manufacturer’s instructions (Revertaid First Strand cDNA Synthesis K1622 Kit, Fermentas).
Gene expression analyses
Expression analysis was performed with three independent total RNA extractions (biological repeats). A standard curve was generated for each ZIP gene and VvGAPDH (as housekeeping gene) using a cDNA serial dilution. The resultant PCR efficiency calculations were imported into relative expression data analysis. PCR parameters used were: 94°C for 4 min; 94°C for 1 min, 60°C (annealing temperature) for 1 min, and 72°C for 1 min for 30 cycles; and a final step at 72°C for 7 min. The PCR products were visualized on agarose gels and isolated with the E.Z.N.A gel extraction kit (Omega Bio-Tek Inc.) to determine the primers efficiency. Gene transcript levels were measured by quantitative PCR (qPCR) using a DNA Engine Opticon 2 Cycler System (MJ Research). All reactions were performed using the Brilliant SYBR Green Master Mix (Stratagene) according to the procedure described by the manufacturer. For each sample, qPCR reactions were carried out in triplicate (technical repeats) using 10 μl Master Mix, 0.5 μl 250 nM each primer, 1 μl diluted cDNA and nuclease-free water in a final volume of 20 μl. Fluorescence was measured at the end of each amplification cycle. Amplification was followed by a melting curve analysis with continuous fluorescence data acquisition during the 65–95°C melt. The raw data were manually analyzed and expression was normalized to GAPDH gene (VvGADPH, NCBI/GenBank database accession number CN938023) Ubiquitin gene (VvUBQ, TIGR database accession number TC32075) to minimize variation in cDNA template levels. Primer sets used for qPCR were: VvZIP1.1rtFwd (5′-TGATATACATGGCGCTGG-3′) and VvZIP1.1rtRev (5′-CAGACACAAGAAAGAAAAGACG-3′) for VvZIP1.1; VvZIP2rtFwd (5′-CCATCAACCATCTCGTTGC-3′) and VvZIP2rtRev (5′-CAAACAAGGATCGTTTACAAGC-3′) for VvZIP2; VvZIP3rtFwd (5′-ACGACGAAAACAGCCCAAC-3′) and VvZIP3rtRev (5′-GGAGTCTCACATTGCTTTGC-3′) for VvZIP3; VvZIP4rtFwd (5′-CTGGTCATCGAAGGCATATTCG-3′) and VvZIP4rtRev (5′-AGGCCCCAAAACAAGAATTAGG-3′) for VvZIP4; VvZIP5.1rtFwd (5′-AAGTTGGAGAGCATGAAGG-3′) and VvZIP5.1rtRev (5′-ATTGGTGGAAAGTGAGAGC-3′) for VvZIP5.1; VvZIP6.1rtFwd (5′-GATGACAGTAGTGCGAATGC-3′) and VvZIP6.1rtRev (5′-TGGTCTCAACTCTCAACAAGC-3′) for VvZIP6.1; VvZIP8rtFwd (5′-AGGCCCTCTTCTTCAACTTCC-3′) and VvZIP8rtRev (5′-AGCCATGCCCAATATCAGC-3′) for VvZIP8; VvZIP11.1rtFwd (5′-CACCGGTATTGTCATAGATGC-3′) and VvZIP11.1rtRev (5′-GGAACACACTTCAAGATGAGC-3′) for VvZIP11.1; VvZIP13rtFwd (5′-GTCGACACATGGTCCTTCC-3′) and VvZIP13rtRev (5′-CCGCACTATTTTCCAAAAGC-3′) for VvZIP13; VvGAPDHFwd (5′-TTCCGTGTTCCTACTGTTG-3′) and VvGAPDHRev (5′-CCTCTGACTCCTCCTT GAT-3′) for VvGAPDH; VvUBQFwd (5′-GTGGTATTATTGAGCCATCCTT-3′) and VvUBQRev (5′-AACCTCCAATCCAGTCATCTAC-3′) for VvUBQ. For the Zn treatment assay in pre-veraison berries, a negative control gene, VvWRKY-20 (WRKY transcription factor 20-like, GSVIVT01030046001), whose expression is not altered during metal treatments (unpublished data) was included. The primers for VvWRKY-20 were: VvWRKY-20Fwd (5′-CAACAAACTCCAAGTGCAGAACC-3′) and VvWRKY-20Rev (5′-CACCCCCAAAAAATGAGAAGG-3′).
In order to determine whether VvZIP3 expression is affected by Zn, Vitis vinifera L. cv. Carménère grape clusters were harvested from field-grown vines in a commercial vineyard in the Maule Valley (Central Chile) during the season S3 at the preveraison stage (EL31, PV) . Uniform berries with their respective peduncles were excised under water, and were positioned on perforated plastic trays (Kim trak 25 × 14 cm) so that the cut pedicels protruded through the holes into a dish containing the proper solution . The experimental conditions were: temperature at 25°C and light at 156 W cm-2. 2 mM of ZnCl2 was applied as a dip solution throughout the experiment and distilled water as a control. Eight random berries from each tray were collected at 6 and 24 hours, pooled together and processed for RNA extraction. The experiment included three trays per treatment (Zn and water) and was repeated twice.
Determination of Zn content
Total Zn content was determined in little clusters, flowers and fruits at different developmental stages (pre-veraison, veraison and mature grapes) according to Karla . The reagents used were of high purity (Suprapur, Merck, Darmstadt). The cleaning of the material was fundamental to guarantee the optimum result in analysis. Tissues were washed with deionized water and oven-dried (80°C) to constant weight. The samples were subsequently homogenized and kept in plastic containers for later analysis. Dried tissues were ground into powder, then ashed at 500°C and dissolved in 2 M HCl . The resulting solution was filtered and washed with bidistilled water to a final volume of 50 mL in a pre-treated volumetric flask. The analyses were done in duplicate. The measurements were done by flame atomic absorption spectroscopy (air/acetylene), using a Unicam 969 spectrophotometer with deuterium background corrector. The method of analysis was validated using the SRM-1570 certified reference material (spinach), supplied by the National Institute of Standards and Technology (USA). Replications of the reference material showed good exactness with relative errors varying between 2.2 – 3.4%.
Yeast complementation assay
The following strains of the yeast Saccharomyces cerevisiae were used in this study: wild type parent strain DY1457 (MATa, ade6, can1, ura3, leu2, his3, trp1) and the Zn2+ uptake defective double mutant ZHY3 Δzrt1/Δzrt2 (MATa, his3, leu2, met1, lys2, ura3, zrt1, zrt2) [19, 20]. Growth occurred in yeast potato dextrose or in synthetic defined (SD) medium with 2% (w/v) glucose or galactose, supplemented as necessary . For metal complementation assay, yeast was grown in liquid SD medium (with 2% [w/v] galactose) until OD = 1, and drop assays were performed on SD plates containing different concentrations of Zn (10 μM, 100 μM, 750 μM and 2 mM). Yeast cells were transformed using the S.c. EasyComp Transformation Kit (Invitrogen). The VvZIP3 cDNA was subcloned from the TOPO vector clone (TOPO TA Cloning Vector System, Invitrogen) into the pYES2 plasmid (Invitrogen) using the primers VvZIP3-fwd (5-CATCTGGATCCATGAGCAAGCTTCAGTTCTATCCAT-3) and VvZIP3-rev (5-CCATCTCTCGAGGATTCCACCCCATTTGGCCAGA-3) to introduce the BamHI and XhoI sites (underlined).
Transient expression assay in onion epidermal cells
The intracellular localization of VvZIP3 was determined by monitoring the transient expression of a VvZIP3-mGFP5 translational fusion product in onion epidermal cells after DNA particle bombardment. The coding region of mGFP5, a green fluorescent protein modified for plants  was fused to the XbaI site of the pART7 vector . The VvZIP3 cDNA was subcloned from pYES2-VvZIP3 to the XhoI-KpnI–digested pART7 between the 35 S cauliflower mosaic virus promoter and the octopine synthase terminator and in frame with mGFP5, using the VvZIP3XhoI-fwd (5-CCATCTCTCGAGATGAGCAAGCTTCAGTTCTATC-3) and VvZIP3KpnI-rev (5-CCCCGGTACCCGATTCCACCCCATTTGGCCAGA-3) primers (sites underlined). Gold particles (0.6 μm) coated with the resulting construct was delivered into onion bulb scale epidermal cell layers with a PDS-1000/He Particle Delivery System (Bio-Rad). The bombardment parameters were as follows: discharge pressure of 1100 p.s.i. with a 900 p.s.i. rupture disk, and distance to target tissue of 6 cm. Onion epidermal layers were placed onto MS agar plates before bombardment and incubated at 22°C for 24 h after particle delivery. Viewing of bombarded samples was done with a confocal microscope (Zeiss LSM-510 system).
We thank Dr. Damien Blaudez and Dr. Michel Chalot (Unité Mixte de Recherche INRA/Université Henri Poincaré “Tree–microbe Interactions”, Faculty of Sciences and Technology, Nancy University, France) and Dr. Sebastien Duplessis (INRA-Nancy, France) for providing the yeast strains and for collaboration in this work. This work was supported by FONDEF G07I1003. FGC, RPC, SG and RP were supported by Universidad de Talca doctoral fellowships.
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