The glutamine synthetase gene family in Populus
© Castro-Rodríguez et al; licensee BioMed Central Ltd. 2011
Received: 6 May 2011
Accepted: 25 August 2011
Published: 25 August 2011
Glutamine synthetase (GS; EC: 18.104.22.168, L-glutamate: ammonia ligase ADP-forming) is a key enzyme in ammonium assimilation and metabolism of higher plants. The current work was undertaken to develop a more comprehensive understanding of molecular and biochemical features of GS gene family in poplar, and to characterize the developmental regulation of GS expression in various tissues and at various times during the poplar perennial growth.
The GS gene family consists of 8 different genes exhibiting all structural and regulatory elements consistent with their roles as functional genes. Our results indicate that the family members are organized in 4 groups of duplicated genes, 3 of which code for cytosolic GS isoforms (GS1) and 1 which codes for the choroplastic GS isoform (GS2). Our analysis shows that Populus trichocarpa is the first plant species in which it was observed the complete GS family duplicated. Detailed expression analyses have revealed specific spatial and seasonal patterns of GS expression in poplar. These data provide insights into the metabolic function of GS isoforms in poplar and pave the way for future functional studies.
Our data suggest that GS duplicates could have been retained in order to increase the amount of enzyme in a particular cell type. This possibility could contribute to the homeostasis of nitrogen metabolism in functions associated to changes in glutamine-derived metabolic products. The presence of duplicated GS genes in poplar could also contribute to diversification of the enzymatic properties for a particular GS isoform through the assembly of GS polypeptides into homo oligomeric and/or hetero oligomeric holoenzymes in specific cell types.
Glutamine synthetase (GS; EC 22.214.171.124, L-glutamate: ammonia ligase ADP-forming) catalyzes the ATP-dependent addition of ammonium (NH4+) to the γ-carboxyl group of glutamate to produce glutamine and acts as the center for nitrogen flow in plants. Glutamate synthase (Fd-GOGAT, EC 126.96.36.199; NADH-GOGAT, EC 188.8.131.52) then catalyzes the conversion of glutamine and 2-oxoglutarate to produce two molecules of glutamate, one of which participates in further ammonium assimilation via GS while the other donates reduced nitrogen for all nitrogen-containing biomolecules . The ammonium assimilated by GS in the production of glutamine can come from various sources, including direct uptake from the soil, reduction of nitrate and nitrite, photorespiration, deamination of phenylalanine catalyzed by phenylalanine ammonia-lyase, and the catabolic release of ammonium during the mobilization of vegetative storage proteins and during senescence.
Multiple nuclear encoded GS polypeptides are expressed in photosynthetic and non-photosynthetic tissues of higher plants and these polypeptides are assembled into oligomeric isoenzymes located either in the cytosol or in the chloroplast [2, 3]. Recently it has been reported that plant GS holoenzyme has a decameric structure composed of two face-to face pentameric rings of subunits, with active sites formed between every two neighboring subunits within each ring [4, 5]. Phylogenetic studies of nucleotide and amino acid sequences have shown that genes for chloroplastic and cytosolic GS in plants form two sister groups with a common ancestor which diverged by duplication before the split between angiosperms and gymnosperms .
In angiosperms there are two main isoforms of GS, cytosolic GS (GS1) and a chloroplastic GS (GS2). This suggests that there are several distinct pathways for glutamine production, both spatially and temporally. In developing leaves, glutamine is mainly produced in chloroplasts through the activity of the GS2 isoenzyme. The ammonium assimilated into glutamine in young leaves is produced by nitrate reduction and through photorespiration [7, 8]. Alternatively, cytosolic GS1 primarily generates glutamine for intercellular nitrogen transport. The cytosolic enzyme assimilates ammonium taken up from the soil and released in the biosynthesis of phenylpropanoids and nitrogen remobilization [9–11]. Thus, GS1 genes are differentially expressed in roots and in vascular tissues. Molecular analysis of genomic GS sequences from a number of angiosperm species has shown that the cytosolic GS1 genes belong to a small multigene family, whereas, the chloroplastic GS2 is encoded by a single gene [9, 10].
GS plays a fundamental role in growth and development of woody plants [11, 12]. In poplar, this critical role for GS has been clearly demonstrated through studies of transgenic poplars that express ectopically the pine cytosolic GS. Transgenic poplars exhibit enhanced vegetative growth [13, 14], enhanced resistance to drought stress at both ecophysiological and enzymatic and non-enzymatic antioxidant levels , and enhanced nitrogen use efficiency . These results clearly lead to the conclusion that in poplar GS activity is a limiting factor in growth and development. The current work was undertaken to develop a more comprehensive understanding of molecular and biochemical features of GS gene family in poplar, to establish an understanding of the roles of specific members of the poplar GS gene family during development, and to characterize the developmental regulation of GS expression in various tissues and at various times during the poplar perennial growth.
Identification and structural analysis of poplar GSgenes
List of GS gene sequences containing a complete open reading frame (ORF) in the genome of Populus trichocarpa
U: 47894.2 P: 42291.5
U: 6.48 P: 5.34
U: 47746.9 P: 42172.2
U: 6.48 P: 5.33
Comparative analysis of GSgene families in sequenced plant genomes
Regulatory regions in the poplar GSgenes
Organ-specific expression of duplicate GSgenes in poplar
In order to investigate the correspondence of GS trancripts and GS polypeptides in the different organs, total proteins from the same protein samples (leaves, stems and roots) were also separated by two-dimensional gel electrophoresis (2D-PAGE), and the GS polypeptides identified by western blotting (Figure 6B). This experimental approach allowed us to identify GS polypeptides of different charge among the family of GS polypeptides of the same size. Thus, in the leaf lamina the GS2 polypeptide was resolved as several spots with the most abundant exhibiting a calculated isoelectric point (pI) of 5.26. The GS1 polypeptide was resolved as a major spot of a pI of 5.52. In the stem, two major major spots corresponded to GS1 polypeptides of pI 5.20 and 5.81. Finally, in the roots the major GS1 spot had a calculated pI of 5.14. These experimental pI values were in the range of the predicted pI values for poplar GS polypeptides (Table 1).
Seasonal changes in GS gene expression
The GS gene family in poplar consists of 8 different genes which exhibit all structural and regulatory elements to be potentially considered as functional genes (Table 1). A detailed analysis of the genomic GS sequences suggests that the GS gene family in poplar is organized into 4 groups of duplicated genes, PtGS1.1, PtGS1.2, PtGS1.3 and PtGS2. These GS genes are distributed on separate loci in different chromosomes, and to our knowledge, Populus trichocarpa is the first plant species in which the complete GS family is observed to be duplicated. However, the duplication of a single GS gene has been previously reported in plants. Thus, two copies of GS1 genes have been described in Pisum sativum , and more recently the occurrence of two distinct GS2 genes have been reported in Medicago truncatula . Homology-microsynteny analysis of the genomic regions where the GS genes are located strongly suggests that the origin of the duplicated genes is a genome-wide duplication event that occurred approximately 65 Myr and which is still detectable over approximately 92% of the poplar genome . Following duplication, new copies of a gene may undergo modifications allowing functional diversification, which is a significant source of evolutionary novelty in plants . However, it is also possible that a duplicated gene copy is rapidly lost through pseudogenisation. Interestingly, the exon-intron organization is highly conserved in each pair of duplicated genes in poplar and similar regulatory elements are present in their promoters. These findings provide evidence supporting the expression of GS duplicates in the same cell-types where they are subjected to similar developmental and environmental cues. Furthermore, their coding regions are also quite well-conserved, indicating they encode for essentially the same or very similar GS enzymes. All these results suggest that these duplicated genes could play equivalent roles in poplar nitrogen metabolism.
The molecular and functional analyses of GS gene families in other plants revealed specialization of GS isoenzymes to fulfil specific and non-overlapping roles in nitrogen metabolism depending of the tissue and plant species [9, 10]. Phylogenetic analyses of poplar GS genes have shown that genes encoding chloroplastic and cytosolic isoforms form two sister groups as previously described for other GS gene families . It has been suggested that the two groups of genes (GS1 and GS2) diverged by duplication from a common ancestor  and that this separation occurred before the divergence of gymnosperms/angiosperms  but possibly after the appearance of vascular plants . It has been proposed that the gain of a N-terminal transit peptide in GS2 would provide adaptive advantages to plants through enhanced photorespiratory ammonium assimilation in the plastids . Members of the GS1 clade in angiosperms are grouped in subfamilies as previously reported by others [6, 10, 21]. PtGS1.2 and PtGS1.3 duplicates were found associated to these subfamilies suggesting they could play similar functions to those described for these isoforms. In contrast, the PtGS1.1 duplicate was found separated from PtGS1.2 and PtGS1.3 genes.
The intron-exon organization of the poplar GS genes supports the above hypothesis (Figure 3). The positions and lengths of exons are quite similar for all genes suggesting that the structure of the ancestral GS gene has been maintained during evolution with some modifications, such as the presence of a plastid targeting sequence in the first exon of GS2 and minor changes in some other exons of GS1 genes.
A detailed analysis of GS transcript abundance in different tissues and organs of poplar allowed us to identify specific expression patterns of the individual members of the gene family (Figures 5 and 7). PtGS2 transcripts were most abundant in leaves as previously reported for other angiosperms where the GS2 isoform is responsible for assimilation of photorespiratory ammonium [9, 10]. In fact, the promoters of the poplar GS2 duplicates contained cis regulatory elements described in other GS2 genes in angiosperms . An additional role of GS2 is the assimilation of nitrate-derived ammonium in leaves. It is well known that plants differ in the localization of nitrate reduction and assimilation. Thus, some species localize nitrate reduction and assimilation in the roots, whereas other species assimilate nitrate preferentially in the leaves. In poplar, most nitrate assimilation takes place in the leaves . Therefore, high levels of the GS2 isoform are necessary to assimilate the ammonium generated by nitrate reduction within the chloroplast.
Only one of the three PtGS1 duplicates in poplar, PtGS1.1, was also preferentially expressed in leaves and interestingly its expression pattern spatially complemented the observed expression pattern of PtGS2. Thus, PtGS1.1 transcripts were particularly abundant in the older leaves located at the basal part of the tree. These results suggest a relevant role of PtGS1.1 in glutamine biosynthesis associated to photosynthetic metabolism in leaves. Furthermore, the presence of light-regulation boxes [26, 27] in the promoter regions of PtGS1.1 duplicates (Figure 4) is consistent with our data and may explain the above described expression pattern in green leaves.
Poplar GS1.2 was preferentially expressed in roots of young trees suggesting a role for this gene duplicate in primary assimilation of nitrogen from soil, as it has been previously described for other cytosolic GS enzymes in plants [28–30]. Interestingly, the relative abundance of PtGS1.2 transcripts increased significantly (12 fold) in poplar leaves infected with Pseudomonas syringae, whereas the expression of other members of the GS gene family was not affected (data not shown). The induction of a GS1 gene in response to pathogen attack has been previously described [31, 32]. Moreover, it has been demonstrated in infected tomato leaves and senescing tobacco leaves that the cytosolic isoform involved in nitrogen remobilisation is the product of a GS1 gene preferentially expressed in roots [33, 34]. These data, together with our work described here suggest that PtGS1.2 may have a role in nitrogen remobilization during leaf senescence.
In young trees, the maximum expression levels of the twin PtGS1.3 genes were detected in stems and petioles. Furthermore, this member of the poplar GS family exhibited the highest levels of gene expression suggesting it plays an essential role in nitrogen metabolism. The regulatory regions of the PtGS1.3 duplicates contained AC elements involved in the interaction with members of the R2R3 Myb factors regulating the transcription of genes for lignin biosynthesis [35, 36]. Similar cis-regulatory elements and trans-acting factors have been found to coordinate lignin biosynthesis and nitrogen recycling in pine , suggesting that PtGS1.3 is involved in nitrogen recycling associated to lignification in poplar. Transcriptomic analyses have also suggested a role of Dof family members in the regulation of genes under conditions resulting in increased lignin deposition . The differential regulation of cytosolic GS genes in conifers by a member of the Dof family (Dof5) was recently reported  and putative regulatory elements for Dof regulation have been identified in poplar GS genes (Figure 4). Furthermore, we have found that orthologous Dof factors are also involved in the regulation of GS isoforms in poplar (García-Gutiérrez, Avila C, Cánovas FM, unpublished data). The analysis of GS polypeptides in different poplar organs by 2D-PAGE (Figure 6) largely confirmed the expression patterns determined for the duplicated GS genes. The GS polypeptides were resolved in four major spots with differential accumulation in poplar organs. Thus, in the leaves, the GS2 and GS1 polypeptides displayed pI values in the range of the calculated pI values for the PtGS2 and PtGS1.1 gene expression products (Table 1). In stems, the predominant GS1 polypeptide is predicted to be the expression product of the PtGS1.3 duplicate whereas the major GS1 polypeptide in roots is predicted to be the expression product of PtGS1.2. This conclusion is supported by the close similarity between the pI values of the GS1 isoforms separated in Figure 6 and the corresponding values deduced from the polypeptides encoded by the PtGS1.3 and PtGS1.2 duplicates (Table 1).
The analysis of transcripts in adult trees during one year of growth (Figure 7) showed that the expression of the poplar GS family members is seasonally regulated. The expression of the PtGS2 duplicate was high in leaves in spring when photosynthesis and photorespiration are at maximum levels . Furthermore, glutamine is required to initiate vegetative protein accumulation during new shoot development in spring . Developing leaves represent a strong sink for nitrogen during active growth . High levels of PtGS1.1 gene expression were also found in leaves of adult trees in summer and autumn when the expression of PtGS2 is very low. These data suggest that the GS1.1 isoform could play an important role in the redistribution of nitrogen from poplar leaves to stems during summer and autumn. In leaves, stem, buds and bark of adult trees, extremely low levels of PtGS1.2 transcripts were detected in winter and summer, however, slight increases were observed in spring and autumn. Nitrogen mobilisation in poplar is seasonally regulated with recycling and transport of nitrogen compounds from senescing tissues to storage tissues in autumn and remobilisation of nitrogen reserves to support active growth in spring . In adult trees, PtGS1.3 gene expression was seasonally regulated with particularly high transcript levels in spring and autumn. Transcript abundance was much high in heterotrophic tissues such as stem, buds and bark, with the exception of senescent leaves in autumn.
The role of cytosolic GS in poplar growth and biomasss production has been reported previously [13, 14]. Furthermore, enhanced GS expression in poplar results in enhanced efficiency of nitrogen assimilation . The role of GS1 in ammonium assimilation and nitrogen remobilisation is particularly important in perennial plants that are able to cope with recurrent periods of growth and dormancy. For example, trees divert large amounts of carbon to the biosynthesis of phenylpropanoids needed to generate lignin, an important constituent of wood. Although lignin does not contain nitrogen, during wood formation there is significant release of nitrogen in the form of ammonium when phenylalanine is deaminated and channeled into lignin biosynthesis and when glycine is decarboxylated in C1 metabolism. These two metabolic pathways are active in lignifying cells . Ammonium ions released must be reintegrated into metabolism in order to maintain high rates of lignification without affecting nitrogen economy [12, 44]. In fact, poplar GS1 transcripts and polypeptides accumulate in developing xylem cells where activities of enzymes involved in the phenylpropanoid pathway and C1 metabolism are high and, therefore, ammonium is liberated [45, 46]. According to these findings we decided to examine in silico the expression of GS genes during wood formation in hybrid poplar (Populus tremula x Populus tremuloides) using the microarray data available in Populus DB . Principal component analysis (Additional file 1) showed a high degree of co-expression for PtGS1.3 and relevant genes involved in lignin biosynthesis and C1 metabolism. In contrast, other members of the GS family also expressed during poplar wood formation (PtGS1.1 and PtGS2) did not show such correlation. Taken together, these data suggest an essential role of PtGS1.3 in lignifying tissues of poplar.
Our analysis shows that Populus trichocarpa is the first plant species in which it was observed the complete GS family duplicated. Considering all data in the present paper, it appears that GS genes have been highly conserved following whole-genome duplication in poplar. In contrast, duplicated members of other gene families in poplar have rapidly diverged [48, 49]. Some authors argue that genes involved in transcriptional regulation and developmental genes are preferentially retained . It has also been proposed that one of the factors influencing the probability of duplicate gene retention is its connectivity . Our data suggest that GS duplicates could have been retained in order to increase the amount of enzyme in a particular cell type. This possibility could contribute to the homeostasis of nitrogen metabolism in functions associated to changes in glutamine-derived metabolic products. It has been reported that recently duplicated genes play an important role in the functional compensation of metabolic products in Arabidopsis . The presence of duplicated GS genes in poplar could also contribute to diversification of the enzymatic properties for a particular GS isoform through the assembly of GS polypeptides into homo oligomeric and/or hetero oligomeric holoenzymes in specific cell types. Further research is needed to confirm these hypotheses.
Experiments were performed with hybrid poplar (Populus tremula x Populus alba, clone INRA 717 1-B4, Institut National de la Recherche Agronomique, INRA). For the expression analysis in different plant organs, plants were micropropagated in vitro on half-strength Murashige and Skoog medium (MS) as described previously . Unless otherwise noted, plantlets were maintained under conditions described previously [13, 14]. Rooted shoots were transferred to plant growth chambers in plastic pots containing a potting mix (HM3-Agromálaga, Málaga, Spain) and vermiculite in proportions 1:1. After ex-vitro acclimatization, the plantlets were maintained for 8 weeks in the following conditions: temperature was kept constant at 22°C, day-length was set at 16 hours, light was supplied at an intensity of 125 μmol m2 s-1 and humidity was fixed about 80%. Plants were regularly supplied with a nutrient solution containing 10 mM potassium nitrate. At the end of the growing period, P. tremula x P. alba plants were harvested and samples taken from 15 different sections from the shoot apex to the root tip.
The aerial regions of the plants was divided into four parts: the apical bud (A), the 1st, 2nd, 3rd, 4th and 5th apical leaves (A1); the intermediate region with the 6th, 7th, 8th, 9th and 10th leaves (A2), and the more basal region including 11th, 12th, 13th, 14th and 15th leaves (A3). Each section was further divided in: L, leaf lamina; V, principal midrib; P, petiole; S, stem. The root was sectioned in R1, principal root and R2, secondary root.
Seasonal analysis of gene expression was monitored in 10-year-old trees of hybrid poplars located in the experimental centre Grice-Hutchinson, Barrio de San Julián, 29004, Málaga, Spain. The samples used were leaves, stems, buds and bark from hybrid trees. The samples were harvested in mid- March, June, September and December of 2008.
Identification of GS gene duplicates and chromosomal mapping
The GS nucleotide and protein sequences were identified using the Eukaryotic Orthologous Groups section of the Join Genome institute (http://genome.jgi-psf.org/Poptr1_1/Poptr1_1.home.html). The protein identifiers used in this genome portal have been conserved in our study (Table 1). GS sequences captured from the poplar database were annotated by blastp searches in the GenBank (http://blast.ncbi.nlm.nih.gov/Blast.cgi). The p-distances among the exonic and intronic regions of the GS family were calculated with the phylogenetic program MEGA 4 , sewing the intron sections of each gene in continuous sequence. The degree of identity between the genomic regions in which the GS duplicated genes were located was explored by using a strategy of searching microsynteny among the different Linkage Groups. Upstream and downstream genomic sequences were aligned with CLUSTALW  and the ORF sequences flanking the GS genes were located manually. Results were then compared with those reported by .
Sequence and phylogenetic analysis
The alignment of the Populus trichocarpa GS protein sequences was carried out with CLUSTALW . The protein sequences used in the construction of the phylogenetic tree were collected from species whose genomes have been fully sequenced. Additionally, sequences of other interesting arboreal species, including Pinus or Picea, have been included. The protein sequences, and their corresponding identifiers, were found in the following databases:
Populus trichocarpa and Sorghum bicolor: http://genome.jgi-psf.org/
Pinus sylvestris and Picea sitchensis: http://www.ncbi.nlm.nih.gov/Genbank/index.html.
Arabidopsis thaliana: http://www.arabidopsis.org/
Oryza sativa: http://rice.plantbiology.msu.edu/
Vitis vinifera: http://www.phytozome.net/
The phylogenetic tree was constructed using the phylogeny platform http://www.phylogeny.fr/ and comprised the following steps. Sequences were aligned using T-Coffee (v6.85) using the 10 best local alignments (Lalign_pair), an accurate global alignment (slow_pair). After alignment, ambiguous regions were removed with Gblocks (v0.91b). Minimum length of a block after gap cleaning was set at 10; no gap positions were allowed in the final alignment. All segments with contiguous non-conserved positions greater than 8 were rejected. The minimum number of sequences for a flank position was set at 85%. The phylogenetic tree was reconstructed using the neighbor joining method implemented in the BioNJ program, using as substitution model a Dayhoof PAM matrix and including 1000 bootstraps. Distances were calculated using ProtDist. The DAY substitution model was selected for the analysis .
The presence of regulatory elements in the 5'-upstream region of poplar GS genes was analyzed starting in the ATG codon of initiation of translation. Sequences for each pair of duplicated genes were aligned by means of MultAlin  in order to locate common regions, and those showing high identity were analyzed to identify putative cis regulatory elements in the plant databases PLACE  and PlantCARE . Sequence stretches of 600 base pairs for the GS1 genes and 1300 base pairs for GS2 genes were compared. More distant regions were not considered, because the p-distance values in these regions showed that similarity between the duplicated sequences diminished considerably.
RNA extraction and cDNA synthesis
Samples from photosynthetic tissues (0.25 g) or non-photosynthetic tissues (0.5 g) were ground under liquid nitrogen with a mortar and pestle in proportions 1:2 and 1:1, respectively. RNA extraction was performed as described by Canales et al.  with minor modifications. The RNA was quantified with a NanoDrop ® ND-1000 spectrophotometer (NanoDrop Technologies, Inc. Wilmington, USA). The integrity of RNA in the samples was verified by agarose gel electrophoresis.
The cDNA synthesis was performed by means of the PrimeScriptTM RT reagent (Perfect Real Time) of Takara BIO Inc. (Otsu, Shiga Japan), following the instructions recommended by the manufacturer. The reaction mix contained 0.5 μg of total RNA in a final volume of 10 μL, which were incubated during 15 min at 37 °C.
Real-time quantitative PCR (qPCR)
The 3' untranslated regions of PtGS1.1, PtGS1.2, PtGS1.3 and PtGS2 duplicates were compared to identify sequences with high identity for each pair of duplicated genes. Oligonucleotide primers were designed to amplify specifically the transcripts encoded by each pair of duplicated genes. Sequences of forward and reverse primers follow.
PCR products were verified by melting point analysis at the end of each experiment. The identity of the PCR products for each GS duplicate was tested during protocol development by gel electrophoresis and confirmed by DNA sequencing (Additional file 2).
The relative quantification of the gene expression was carried out by qPCR using a thermal cycler (Real System Stratagene MX Swindles PCR 3000PTM, Agilent Technologies, Santa Clara, CA). The qPCR system was the QUANTIMIX EASY SYG (Biotools B&M Labs S.A. Madrid, Spain) and the protocols followed were those recommended by the manufacturer. The PCR reactions were performed by triplicate using samples without DNA as controls. The volume of the qPCR samples was 2 μL containing 10 ng of cDNA from the RT reactions. The amplification program had 3 steps: i) 1 cycle (95°C, 2 min); ii) 40 cycles, cDNA denaturing (95°C, 15 s), hybridization (55°C, 15 s) and extension (72°C, 30 s); iii) 1 cycle (95 °C, 1 min) and 1 cycle (30 s) for absolute temperatures from 55°C to 95°C to generate the dissociation curve in order to confirm the specific amplification of each individual reaction.
The relative expression levels were calculated by using actin2 and ubiquitin as reference genes . The initial number of transcripts of the candidate and reference genes (N0) was calculated by means of the LinRegPCR software version 11.0 . The normalized N0 was found by calculating the ratio between the averages of the N0 of the replicates and the N0 of the reference genes (normalization factor).
Protein extraction and western blot analysis
Poplar protein extraction was performed using the following protocol. One gram of plant tissue was homogenized in mortar and pestle with 1 g of sand and 1 mL of extraction buffer [0.175 M Tris pH 8.8, 5% SDS (w/v), 15% glycerol (v/v), 0.3 M mercaptoethanol]. The extract was then centrifuged at 10,000 × g, 4°C for 30 min. The supernatant was mixed with 4 volumes of acetone for 1 h at -20°C and then centrifuged at 10,000 × g 4°C for 30 min. The resulting pellet was washed with 80% (v/v) acetone and centrifuged two times at 10,000 × g 4°C for15 min. The pellet was dried and solubilized in loading buffer for SDS-electrophoresis on 12.5% (w/v) polyacrylamide gels. Resolved polypeptides were electrotransferred onto nitrocellulose membranes (Whatman GmbH, Dassel, Germany) and the presence of GS polypeptides was immunorevealed as described by Cánovas et al.  using the antiserum raised against recombinant pine GS . Subsequent detection of immunocomplexes was carried out by a peroxidase assay.
Two-dimensional gel electrophoresis
Two-dimensional gel electrophoresis was carried out as described previously . Poplar proteins were solubilized in isoelectrofocusing (IEF) loading buffer. The amount of protein loaded per gel was 30 μg. IEF slab gels were 80 × 70 × 1 mm consisting of 5% (w/v) polyacrylamide, 8.3 M urea, 2.5% (v/v) carrier ampholytes (Pharmalyte pH 4-6). IEF was performed at 200 V for 2.5 h. The second dimension electrophoresis was also performed in 80 × 70 × 1.5 mm slab gels of 12.5% (w/v) polyacrylamide gels containing SDS as described above. The resolved proteins were then transferred to nitrocellulose membranes and immunodetection was performed essentially as described for one-dimensional western blots.
This work was supported by a grant from the Spanish Ministry of Science and Innovation (BIO2009-07490) and by research funds from Junta de Andalucía (group BIO114). We thank Juan Antonio Pérez-Claros for helpul advice on statistical analysis and Remedios Crespillo for excellent technical support. We are very grateful to members of the Kirby and Cánovas laboratories for their kind assistance in various aspects of this work. We also thank Antonio de Vicente for his generous gift of the bacterial strain Pseudomonas syringae pathovar tomato. Angel García-Gutiérrez was granted for Dirección General de Innovación Educativa y Formación del Profesorado of Consejería de Educación y Ciencia (Junta de Andalucía, Spain) to expend one year doing research at the Universidad de Málaga. Edward G. Kirby gratefully acknowledges the Ministerio de Educación y Ciencia of Spain for a sabbatical fellowship in the Cánovas lab.
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