Cadmium exposure and sulfate limitation reveal differences in the transcriptional control of three sulfate transporter (Sultr1;2) genes in Brassica juncea
© Lancilli et al.; licensee BioMed Central Ltd. 2014
Received: 1 February 2014
Accepted: 6 May 2014
Published: 16 May 2014
Cadmium (Cd) exposure and sulfate limitation induce root sulfate uptake to meet the metabolic demand for reduced sulfur. Although these responses are well studied, some aspects are still an object of debate, since little is known about the molecular mechanisms by which changes in sulfate availability and sulfur metabolic demand are perceived and transduced into changes in the expression of the high-affinity sulfate transporters of the roots. The analysis of the natural variation occurring in species with complex and highly redundant genome could provide precious information to better understand the topic, because of the possible retention of mutations in the sulfate transporter genes.
The analysis of plant sulfur nutritional status and root sulfate uptake performed on plants of Brassica juncea – a naturally occurring allotetraploid species – grown either under Cd exposure or sulfate limitation showed that both these conditions increased root sulfate uptake capacity but they caused quite dissimilar nutritional states, as indicated by changes in the levels of nonprotein thiols, glutathione and sulfate of both roots and shoots. Such behaviors were related to the general accumulation of the transcripts of the transporters involved in root sulfate uptake (BjSultr1;1 and BjSultr1;2). However, a deeper analysis of the expression patterns of three redundant, fully functional, and simultaneously expressed Sultr1;2 forms (BjSultr1;2a, BjSultr1;2b, BjSultr1;2c) revealed that sulfate limitation induced the expression of all the variants, whilst BjSultr1;2b and BjSultr1;2c only seemed to have the capacity to respond to Cd.
A novel method to estimate the apparent kM for sulfate, avoiding the use of radiotracers, revealed that BjSultr1;1 and BjSultr1;2a/b/c are fully functional high-affinity sulfate transporters. The different behavior of the three BjSultr1;2 variants following Cd exposure or sulfate limitation suggests the existence of at least two distinct signal transduction pathways controlling root sulfate uptake in dissimilar nutritional and metabolic states.
KeywordsBrassica juncea Cadmium Sulfate limitation High-affinity sulfate transporters
Sulfur is an essential element for all living organisms, since it is found in a broad variety of biological compounds playing pivotal roles in a number of metabolic processes . In contrast to animals, which have a dietary requirement for some organic sulfur compounds, plants have metabolic pathways that allow them to assimilate inorganic sulfur into organic sulfur compounds through a cascade of well characterized enzymatic steps. For this reason plant sulfur assimilatory pathways are considered to be the main sources of organic sulfur compounds for animal and human diets .
The main sulfur source for plants is the sulfate ion of the soil solution available in the rhizosphere [3, 4], which is taken up through specific root plasma membrane high-affinity sulfate transporters. Once inside the plant, sulfate is allocated to different sinks, and undergoes intracellular channeling to chloroplast and vacuole, where it is assimilated into organic sulfur compounds or compartmentalized as sulfur store, respectively . The main pathway of sulfate assimilation in plants involves the adenylation of the anion and its stepwise reduction to sulfite and then sulfide which is finally incorporated via O-acetylserine (OAS) into cysteine (Cys), a key intermediate from which the essential amino acid methionine (Met), the tripeptide glutathione (GSH), and most sulfur containing compounds are synthesized [2, 5].
Considering the central role of Cys in sulfur metabolism, it appears evident that both sulfate uptake and the reductive assimilation pathway have to be finely modulated to meet the metabolic demand for sulfur arising from Cys consuming activities, which largely contribute to define the total sulfur requirement of plants. Such a demand may consistently vary under the different environmental conditions that plants may experience during their growth. For instance, biotic and abiotic stresses may increase the metabolic demand for some Cys derived compounds, causing an increase in the activity of the sulfate assimilatory pathway . An example of this has been largely described in plants exposed to cadmium (Cd) in which the activation of a wide range of adaptive responses involving GSH consuming activities may increase the demand for sulfate, sulfur metabolites and carbon skeletons [7–10]. Indeed, GSH not only acts as an antioxidant in mitigating Cd-induced oxidative stress, but also represents the key intermediate for the synthesis of phytochelatins (PCs), a class of Cys-rich heavy metal-binding peptides involved in buffering cytosolic metal-ion concentration . The large amount of PCs produced by Cd stressed plants represents an additional sink for reduced sulfur which, by increasing the metabolic request for both Cys and GSH, generates a typical demand-driven coordinated transcriptional regulation of genes involved in sulfate uptake, sulfate assimilation and GSH biosynthesis. Such a response is thought to be essential to satisfy two contrasting needs arising from Cd stress: i) maintaining cell GSH homeostasis; ii) detoxifying heavy metals by means of GSH-consuming activities. A similar activation has been described under sulfate limitation [12–14], although in this condition plant sulfur needs to sustain the growth do not vary: the induction of sulfate transporters and enzymes along the assimilatory pathway reflects some difficulties in maintaining both an adequate rate of Cys biosynthesis and sulfur-containing compound homeostasis.
Sulfate transport activations under Cd stress and sulfate limitation have been shown to be mainly controlled at transcriptional level and have been often indicated as resulting from the same, although controversial, nutritional signals [8, 9, 15]. In the current model of transcriptional regulation, some intermediates along the pathway of sulfate assimilation and GSH biosynthesis act as negative or positive signals in modulating the expression of sulfate transporters. Adequate levels of reduced sulfur compounds, such as Cys and GSH, would repress gene expression through a negative feedback loop preventing excessive sulfate uptake and reduction; vice versa a contraction of GSH pools would de-repress gene transcription allowing sulfate to enter the pathway. A second regulatory loop, involving OAS as a key intermediate, should act in promoting gene de-repression when nitrogen and carbon supply exceeds sulfur availability within the cells. In this condition, since sulfide availability is not enough for Cys biosynthesis, OAS accumulates and partially overrides the negative feedback provided by GSH on gene transcription . Such a reversible regulation allows the system to adjust sulfate uptake to the nutritional status of the plant, and agrees with the concept of demand-driven regulation of sulfate uptake and metabolism .
Comparative studies clearly show that both sulfate deprivation and Cd stress produce a contraction in the GSH pools and a positive change in the OAS levels, which in turn may induce the accumulation of high-affinity sulfate transporter mRNAs, allowing sulfate to enter the cells . However, some aspects of this picture need to be further investigated, since the relationships existing between the accumulation of sulfate transporter mRNAs and the levels of the signal-intermediates do not always appear to be evident [9, 17]. Moreover, Rouached and co-workers  clearly showed that the expression of the Arabidopsis Sultr1;1 and Sultr1;2 – two high-affinity sulfate transporter genes – is not regulated in complete agreement with the current model, and they proposed the existence of distinct signaling pathways controlling sulfate uptake under different sulfur nutritional status. Finally, whether cellular contents of sulfate, sulfide, OAS, Cys and GSH are the true primary signals for controlling sulfate uptake and reduction or rather act indirectly is still a matter of investigation [14, 18], since very little is known about the molecular mechanisms involved in the nutritional signal perception and transduction [2, 19, 20]. Thus the need for additional efforts and integrated experimental approaches appears particularly evident to unveil this picture. The analysis of the natural variation occurring in species with redundant genomes could provide precious information about the molecular mechanisms controlling sulfate uptake, since the presence of redundant genes may have led to the accumulation of mutations which otherwise would have been eliminated by natural selection. From this point of view the species belonging to the Brassica genus could be very useful, since several lines of evidence suggest that the genomes of the three diploid Brassica species (B. rapa, B. oleracea and B. nigra) are composed of three rearranged variants of an ancestral genome – structurally similar to that of Arabidopsis thaliana – and descended from a common mesohexaploid ancestor [21–23]. Moreover the level of complexity may be further increased by considering the allopolyploid Brassica species in which two distinct Brassica genomes cohabit , increasing the probability of evolving novel gene interactions through the processes of sub-functionalization and/or neo-functionalization of paralogs [25, 26].
In this work we present and discuss some evidence toward the existence of multiple transduction pathways controlling sulfate uptake under Cd stress and sulfate limitation in Brassica juncea (AABB, n = 18), a natural occurring allotetraploid species formed through hybridization between B. rapa (AA, n = 10) and B. nigra (BB, n = 8), as described by the “triangle of U” .
Plant material, growth conditions, and experimental design
Brassica juncea L. Czern & Coss (Lodi selection) seeds were sown on filter paper saturated with distilled water and incubated at 26°C in the dark. Three days after sowing, seedlings selected for uniform growth were transplanted into 5 L plastic tanks (6 seedlings per tank) containing an aerated complete nutrient solution [500 μM NH4H2PO4, 3 mM KNO3, 2 mM Ca(NO3)2, 1 mM MgSO4, 25 μM Fe-tartrate, 46 μM H3BO3, 9 μM MnCl2, 0.8 μM ZnCl2, 0.3 μM CuCl2, 0.1 μM (NH4)6Mo7O24, pH 6.5] and kept for 14 days (pre-growing period) in a growth chamber maintained at 26°C and 80% relative humidity, with a 16-h light period. For Cd treatments, plants were grown for an additional 8 days (acclimation period) in a 5-fold diluted (not for micronutrients) nutrient solution (acclimation solution) and then exposed to different Cd concentrations (0, 10, and 25 μM CdCl2) for 48 h. For sulfate limitation treatments, at the end of the pre-growing period plants were grown for 10 days in the acclimation solution containing different sulfate concentrations (200, 50 or 10 μM); in the cases of the lowest sulfate concentrations, MgCl2 was added to maintain the same concentration of magnesium. In both cases the growth chamber parameters were the same as described before, and all hydroponic solutions were renewed twice a week to minimize nutrient depletion. At the end of the experimental periods, plants were immediately used for the in vivo experiments or harvested to be further analyzed. In this case roots were washed for 10 min in ice-cold 5 mM CaCl2 solution to displace extracellular Cd , rinsed in distilled water and gently blotted with paper towels; shoots were separated from roots and the tissues were frozen in liquid N2 and stored at -80°C.
RNA extraction and cDNA cloning
BjSultr1;1 and BjSultr1;2 partial cDNAs were amplified by RT-PCR from Brassica juncea mRNA isolated from roots. Total RNA was extracted from roots of sulfur-starved plants using TRIzol reagent (LifeTechnologies), poly A+ mRNA was isolated using the Oligotex mRNA Spin-Column system (QIAGEN), and first-strand cDNA synthesis was carried out using the SuperScriptIII first-strand synthesis system for RT-PCR (LifeTechnologies) according to the manufacturer's instructions. Degenerate primers BjSultr1;1degdir (5'-ACGGAGGAGGGTCCGRTGCAA-3'), BjSultr1;1degrev (5'-TTYGGGTCGATCACGGCCTGGCA-3'), BjSultr1;2degdir (5'-GTYTTCGATTGGGGRCGTAR-3'), and BjSultr1;2degrev (5'-RAGGAAGAGCAATGTCAAGAGA-3'), were designed based on highly conserved regions identified in sequences of sulfate transporter cDNAs of Brassica napus and Arabidopsis thaliana [for BjSultr1;1: BnSultr1;1 (GenBank accession no. AJ416460) and AtSultr1;1 (TAIR accession no. At4g08620); for BjSultr1;2: BnSultr1;2 (GenBank accession no. AJ311388), and AtSultr1;2 (TAIR accession no. At1g78000)]. 5′- and 3′-regions of the sulfate transporter cDNAs were isolated by 5′- and 3′-RACE approach using GeneRacer Kit (LifeTechnologies) according to the manufacturer's instructions. Finally the full coding regions were confirmed by RT-PCR using sequence specific primers obtained from the 5′- and 3′-RACE fragments, and proofreading Pfu-DNA polymerase (Promega). All PCR products were verified by sequencing after cloning into the pCR-BluntII vector (LifeTechnologies), and sequence data were submitted to GenBank (accession no. JX896426, BjSultr1;1; JX896427, BjSultr1;2a; JX896428, BjSultr1;2b; JX896429, BjSultr1;2c).
Sequence analyses were performed using ClustalW and neighbor-joining trees were generated using MEGA 5.05 .
Gene expression analysis
Semi-quantitative RT-PCR analyses of BjSultr1;1 and BjSultr1;2 pool were performed on first-strand cDNA deriving from total RNA extracted from roots. PCR was carried out for 24 cycles, where cDNAs were exponentially amplified by Pfu-DNA polymerase (Promega), using the following couples of primers: BjSultr1;1dir 5'-ACGGAGGAGGGTCCGATGCAA-3' and BjSultr1;1rev 5'-TTCGGGTCGATCACGGCCTGGCA-3' (producing a 453 bp fragment), BjSultr1;2dir 5'-GGTTTTCGATTGGGGACGTA-3' and BjSultr1;2rev 5'-TGTCAAGAGAACAACGATTGAC-3' (producing 1046 bp overlapping fragments). cDNA loading was normalized using the BjTub 846 bp amplicon (accession no. JX896430), as an internal control, obtained with primers designed on conserved regions of beta tubulin Tub9 sequences of Arabidopsis thaliana (TAIR accession no. At4g20890) and Brassica napus (GenBank accession no. AF258790) as follow: Tubdir 5′-TGTTGTGAGGAAGGAAGCTGAG-3′ and Tubrev 5′-TCCTGTGTACCAATGAAGG-3′. PCR products were separated in agarose gels and stained with SYBR Green I (LifeTechnologies); signals were detected using a laser scanner (Typhoon 9200, GE Healthcare) with a 532 nm laser and a 526 nm filter.
For semi-quantitative RT-PCR analyses of the three different variants of BjSultr1;2, the entire ORFs were amplified with BjSultr1;2ATG 5′-ATGTCTGGGAGAGCTCATCCTG-3′ and BjSultr1;2STOP 5′-TCAGACCTCGTCGGAGAGTTTTG-3′ primers (producing a fragment of 1968 bp for BjSultr1;2a and fragments of 1959 bp for BjSultr1;2b and BjSultr1;2c). PCR products were then digested with ClaI endonuclease at 37°C for 3 h, and restriction products were separated in agarose gels. Signals were detected after staining as above described, and densitometrically analyzed using ImageJ 1.46 software .
All the expression analyses were performed using three independent cDNAs deriving from three independent experiments in which six plants were pooled for RNA extraction. Each cDNA was amplified, digested, run on gel, and quantified three times (n = 9).
Heterologous expression of sulfate transporters and kinetic analysis in yeast
EcoRI-ended fragments, resulting from the amplification of BjSultr1;1, BjSultr1;2a/b/c, ZmST1;1, and AtSultr2;1 ORFs using appropriate primers (BjSultr1;1KATG 5′-CACTAGAATTCTAAAAAATGGCCAAGACTAATCCGCCGGA-3′ and BjSultr1;1KSTOP 5′-TGACCGAATTCTTATGCTTGTTGCTCAGCCAAT-3′, BjSultr1;2KATG 5′-CACTAGAATTCTAAAAAATGTCTGGGAGAGCTCATCCTG-3′ and BjSultr1;2KSTOP 5′- TGACCGAATTCTCAGACCTCGTCGGAGAGTTTTG-3′, ZmST1;1KATG 5′-CAGCGAATTCTAAAAAATGCCGCCGCGAACGGTGTCC-3′ and ZmST1;1KSTOP 5′-GCGCGAATTCTCAGACATTATCGACCATCTTAGGAGC-3′, and AtSultr2;1KATG 5′-CAGCGAATTCTAAAAAATGAAAGAGAGAGATTCAGAGA-3′ and AtSultr2;1KSTOP 5′-TGACCGAATTCTTAAACTTTTAATCCAAAGCAAGCATCAA-3′) including a consensus sequence for translation initiation in yeast , were subcloned in the EcoRI site of the yeast (Saccharomyces cerevisiae) expression vector pESC-TRP (Stratagene) under the control of GAL10 promoter. Chimeric and empty vectors were used to transform the yeast double sulfate transporter mutant CP154-7A (MATα his3 leu2 ura3 ade2 trp1 sul1:LEU2 sul2:URA3)  using the standard lithium acetate method , and Trp+ recombinant yeast cells were selected. Complementation tests were performed as previously described .
For the growth analysis, recombinant yeast cells were grown – at 28°C in a synthetic Trp-free liquid medium containing yeast nitrogen base and required amino acids – up to reach a mid-log phase. Yeast cells were then washed twice with sterile distilled water and resuspended to a final absorbance of 0.1 A600 unit in the B minimal medium , supplemented with 40 μg mL-1 adenine and 200 μg mL-1 histidine to meet the auxotrophies of the strain, and containing different amounts of Na2SO4 or 100 μM DL-homocysteine (HCys) as sole sulfur sources. Yeasts were incubated at 28°C and growth was monitored by measuring the absorbance at 600 nm. At the end of the growing period, 30 mL of the yeast culture was harvested, washed twice in sterile distilled water, resuspended in 4 mL of boiling buffered ethanol (75% ethanol in 10 mM HEPES, pH 7.1) and incubated for 3 min at 80°C. After cooling down the mixture on ice, the volume was reduced by evaporation at 70°C, the residue was resuspended in 4 mL of distilled water and centrifuged for 15 min at 13000 g and 4°C. The supernatant was collected and the sulfate content was then determined according to the turbidimetric method described by Tabatabai and Bremner .
The duplication times of the yeast cells were calculated by fitting the equation A600(t) = A600(t0) ekt to the experimental data. The growth constant (kG) was estimated by expressing the growth rates (dt-1) of complemented yeasts as a function of sulfate concentrations in the media, and by fitting the Michaelis-Menten equation to the data.
Determination of thiols, sulfate and cadmium content
Roots and shoots were pulverized using mortar and pestle in liquid N2. Total nonprotein thiols (NPTs) and Cd contents were determined according to Nocito and co-workers . Total GSH was measured according to Griffith .
Sulfate was extracted by homogenizing the samples in 1:10 (w/v) ice-cold 0.1 N HNO3. After heating at 80°C for 40 min, the extracts were filtered and the sulfate contents were determined according to the turbidimetric method described by Tabatabai and Bremner .
Sulfate influx assay and analysis of root-to-shoot sulfate translocation
Sulfate influxes into the roots were measured by determining the rates of 35S uptake, over a 15 min pulse in incubation solutions labeled with the radiotracer. Briefly, a single plant was placed onto 400 mL of a fresh acclimation solution, containing 200 μM MgSO4, supplemented or not with CdCl2 at different concentrations, aerated and thermoregulated at 26°C. Radioactive pulses were started by adding 35S-labeled Na2SO4 to the uptake solutions. Specific activity was 4.7 kBq μmol-1. At the end of the pulse period, roots were excised from shoots, rinsed twice for 1 min in 400 mL of a 4 mM CaSO4 nonradioactive solution at 4°C, blotted with paper towels, weighed, and then heated for 20 min at 80°C in 0.1 N HNO3 (10 mL g-1 fresh weight). Radioactivity was measured on aliquots of the extracting solution by liquid scintillation counting in a β counter (LS 6000SC, Beckman).
For the analysis of root-to-shoot sulfate translocation, shoots were cut at 2 cm above the roots with a microtome blade. Xylem sap exuded from the lower cut surface was collected by trapping into a 1.5 mL plastic vial filled with a small piece of cotton for 1.5 h. The amount of collected sap was determined by weighing and the sulfate concentration was then determined according to the turbidimetric method described by Tabatabai and Bremner .
Statistical analysis was carried out using SigmaPlot for Windows version 11.0 (Systat Software, Inc.). Quantitative values are presented as mean ± standard error of the mean (SE). Significance values were adjusted for multiple comparisons using the Bonferroni correction. Statistical significance was at P < 0.05. Student’s t-test was used to assess the significance of the observed differences between control and treated plants. Statistical significance was at P ≤ 0.001.
Cloning and functional characterization of four high-affinity sulfate transporter cDNAs
Plant sulfate transporters are encoded by a multi-gene family whose members have specific functions in sulfate acquisition, systemic distribution and subcellular localization [37–39]. In this work we identified four sulfate transporter cDNAs expressed in B. juncea roots: one named BjSultr1;1, and three, with closely related sequences, named BjSultr1;2a, BjSultr1;2b and BjSultr1;2c. All the cDNA-encoded proteins were predicted as putative high-affinity sulfate transporters belonging to the group 1 of the sulfate transporter family (Additional file 1). Sequence analyses revealed that the amino acid identities of these proteins with those of Arabidopsis belonging to the same cluster were 86% (BjSultr1;1 vs AtSultr1;1) and 94% (BjSultr1;2a/b/c vs AtSultr1;2), suggesting that the B. juncea and Arabidopsis sulfate transporters would share functions in mediating root sulfate uptake. In such a way BjSultr1;1 could be considered the ortholog of AtSultr1;1, whereas the three BjSultr1;2 cDNAs would represent three orthologous variants of AtSultr1;2.
Concerning the three BjSultr1;2 forms, some additional data need to be taken into account. Sequence analysis (Additional file 2; Additional file 3) revealed that the coding sequence of the longer variant, BjSultr1;2a, shares 98% of nucleotide identity with Bra015641, a gene encoding a Sultr1;2 form on the chromosome A7 of B. rapa – one of the two parents of B. juncea of which the genome has been recently sequenced  – and only 91% of nucleotide identity with Bra008340, a second form of Sultr1;2 found on the chromosome A2 of B. rapa. On the other hand the coding sequences of the shorter variants, BjSultr1;2b and BjSultr1;2c, share the highest identities with Bra008340 (95% and 99%, respectively). Unfortunately, we failed in finding any information about the sulfate transporter genes of B. nigra (the other B. juncea parent) in public genomic databases.
The heterologous expressions of BjSultr1;1, BjSultr1;2a, BjSultr1;2b, and BjSultr1;2c in the yeast (Saccharomyces cerevisiae) double sulfate transporter mutant CP154-7A  were able to revert the yeast mutant phenotype, allowing it to grow on a minimal medium containing 100 μM Na2SO4 as a sole sulfur source (Additional file 4), confirming the identity of these B. juncea clones as functional sulfate transporters.
Effect of Cd exposure and sulfate limitation on sulfate uptake and sulfur allocation in Brassica junceaplants
All the data presented in this paragraph derived from experiments aimed at comparing environmental conditions (Cd exposure and sulfate limitation) in which sulfate uptake induction should occur. For these purposes plants were exposed to 10 and 25 μM Cd2+ for 2 days or grown under sulfate limitation (50 and 10 μM SO4 2-) for a 10-day period. Control plants were grown at 200 μM SO4 2- in the absence of Cd.
Dry weight of roots and shoots and Cd accumulation
0.063 ± 0.003 (a)
0.241 ± 0.010 (a)
10 μM Cd2+
0.069 ± 0.003 (a)
0.252 ± 0.011 (a)
25.81 ± 1.18 (a)
5.66 ± 0.25 (a)
25 μM Cd2+
0.066 ± 0.004 (a)
0.231 ± 0.012 (a)
97.33 ± 3.99 (b)
5.00 ± 0.22 (a)
50 μM SO42-
0.112 ± 0.005 (b)
0.251 ± 0.011 (a)
10 μM SO42-
0.110 ± 0.005 (b)
0.243 ± 0.011 (a)
Taken as a whole these preliminary results indicate that 48 h Cd exposure and 10-day sulfate limitation produced similar induction of sulfate uptake. Since such effects should presumably be related to changes in the sulfur nutritional status of the plants, we analyzed the levels of NPTs, GSH and sulfate of both roots and shoots, assuming the pools of these intermediates as the main diagnostic indicators of the sulfur nutritional status.
Quantitative analysis of the expression of the three BjSultr1;2variants
Since the three BjSultr1;2 forms are not polymorphic enough to be distinguished by means of a simple PCR (Additional file 8), we developed a suitable method to study changes in their expression by coupling semi-quantitative RT-PCR analysis with the use of an opportune restriction enzyme.
Starting from this rationale, we designed a couple of primers amplifying at the same time the entire open reading frames of the three clones with the same efficiency (data not shown), and we used these oligos for the semi-quantitative RT-PCR analysis of the effects of 48 h exposure to 25 μM Cd2+ or 10-day sulfate limitation (10 μM SO4 2-) on the expression of the three BjSultr1;2 variants. A restriction analysis using the ClaI endonuclease followed the amplification reactions.
By contrast, in the case of sulfate limitation, the increase in the cumulative amount of the BjSultr1;2 transcripts (+455% with respect to the sulfur-sufficient control) was ascribable to changes in the transcript levels of all the three forms (Figure 6C). In particular, the BjSultr1,2a, BjSultr1;2b, and BjSultr1;2c transcript levels significantly increased by 371%, 483%, and 618%, respectively (Figure 6D, Additional file 9).
Brassica juncea (L.) Czern & Coss (AABB, n = 18) is believed to have originated from the interspecific hybridization of two base “diploid” genomes provided by Brassica rapa L. (AA; n = 10) and Brassica nigra L. (BB; n = 8) [24, 40]. Both the diploid parents are thought to be ancient polyploids since they still exhibit highly replicated genomes, each containing three paralogous subgenomes closely related to that of Arabidopsis thaliana [21–23]. In spite of the whole-genome triplication event – thought to have occurred between 13 and 17 million years ago – most comparative studies have shown that the number of each ancestral gene retained in the genome of the modern diploid Brassica is variable, since paralogous regions exhibit interspersed gene losses and insertions. Interestingly, in the recently sequenced B. rapa genome the extent of gene loss among triplicated genome segments varies, with one of the three copies consistently retaining a disproportionately large fraction of the genes expected to have been present in its ancestor . Such evolutionary events are thought to be the biological basis of the immense plasticity of Brassica species and may have led to a diversification of the genes retained in more than one copy, in terms of function and/or expression. Searching for orthologs of the Arabidopsis high-affinity sulfate transporter genes involved in sulfate uptake and retained in the genome of B. rapa – one of the two parents of B. juncea – revealed the existence of three distinct loci, annotated as Bra022623, Bra015641 and Bra008340. The first locus encodes for a putative high-affinity sulfate transporter closely related to Arabidopsis AtSultr1;1, whilst the other two loci encode for two different forms of a high-affinity sulfate transporter functional related to Arabidopsis AtSultr1;2, indicating these gene loci as paralogs. As expected, a much more complex picture was found in the allopolyploid B. juncea in which we were able to identify an orthologous form of AtSultr1;1 (BjSultr1;1) and three orthologous forms of AtSultr1;2 (BjSultr1;2a/b/c). From the results obtained by the sequence analysis, and in the absence of any other information so far available about the B. nigra genome, we can reasonably suppose: i) BjSultr1;2a as the ortholog of Bra015641 on the genome A or B of B. juncea; ii) BjSultr1;2b/c as allelic variants orthologous of Bra008340 on the A or B genome of B. juncea or a homeologous gene pair related to Bra008340 on the A and B genomes of B. juncea. Moreover, since the progeny derived from self-fertilization inherited all the three BjSultr1;2 variants (data not shown), it seems likely to exclude that BjSultr1;2b and BjSultr1;2c would be allelic, making plausible the hypothesis they are instead present at different homeologous gene loci on A and B genomes, each in homozygous configuration; otherwise, a simple mendelian segregation would be observed. In any case, since the three BjSultr1;2 forms would share a common ancestor gene, they may either have retained their original functions and expressions, or – as it is often the case – have accumulated deleterious mutations or have evolved novel gene interactions through the processes of sub-functionalization and/or neo-functionalization [25, 26].
Results of complementation tests in the yeast mutant strain CP154-7A, defective in its two sulfate transporters and thus unable to grow on media containing low concentrations of sulfate as the sole sulfur source , proved the capacity of BjSultr1;1 and BjSultr1;2a/b/c to transport sulfate ions across the plasma-membrane (Additional file 4). Moreover, kinetic analysis of the growth (G) isotherms of complemented yeasts, revealed that BjSultr1;1 and BjSultr1;2a/b/c have high affinities for sulfate, as revealed by the kG values similar to the apparent kM values of other plant high-affinity sulfate transporters [9, 41–44] indicating that all the B. juncea clones have retained their functions. It is also worthy of note that the sulfate transporter BjSultr1;1 has an apparent affinity for sulfate (kG = 5.46 μM) three times lower than those of the three BjSultr1;2 forms (Figure 1). Finally, phylogenetic analyses indicate these transporters as functionally related to AtSultr1;1 and AtSultr1;2 and then we can infer their probable function in mediating root sulfate uptake from the soil solution [14, 43, 44].
Physiological analysis reveals that Cd exposure as well as sulfate limitation induces sulfate uptake in B. juncea roots. Such behaviors seem to be related to the induction of high-affinity sulfate transporters belonging to the group I, as indicated by the increase in the transcript levels of BjSultr1;1 and BjSultr1;2 pool (Figure 2). Thus – at the physiological level – B. juncea also retains the typical responses of sulfate uptake to Cd or sulfur shortage [9, 15]. The apparent quantitative discrepancy between the changes in the transcript levels of BjSultr1;1 and BjSultr1;2 pool and the resulting increases in sulfate uptake may be due to additional regulatory mechanisms working in parallel with the transcriptional control of the high-affinity sulfate transporter genes .Considering the current model of demand-driven regulation of sulfate uptake, such inductions should be related to the sulfur nutritional status reached by plants in the two growing conditions. Changes in the amounts of sulfur-containing compounds that we assume as the main diagnostic indicators of the sulfur nutritional status of root and shoot clearly indicate that Cd exposure and sulfate limitation influence sulfur allocation throughout the whole plant, generating deeply different local nutritional states which make it difficult to individuate an unequivocal and common nutritional signal related to the expression of sulfate transporters (Figure 3). Indeed, as expected, lowering sulfate concentration in the external medium necessarily results in a significant contraction of all the analyzed sulfur pools of the roots, whilst Cd stress produces a typical increase in the level of NPTs, probably due to the activation of GSH-dependent PC biosynthesis, without affecting the sulfate content of the roots.
Root responses to Cd exposure seem to be due to homeostatic mechanisms driven by increases in the sulfur need of the plants, since, as previously reported , the effect of Cd on sulfate uptake capacity is closely related to the NTP levels of both root and shoot and then to the strength of the Cd-induced additional sink for thiols (Additional file 11). Under Cd exposure the NPT levels in plant tissues significantly increase, reaching values 8.5 (root) and 1.3 (shoot) fold higher than in the control at the highest concentration analyzed. Since the sulfate pools of both root and shoot seem not to be affected by Cd exposure, it appears clear that the additional sulfur required to sustain thiol biosynthesis necessarily derives from the activation of sulfate uptake. On the other hand, root responses to sulfate shortage appear likely to be dependent on the need for allocating the limiting nutrient in the best and most efficient way. In fact, the stepwise decrease in the sulfate content of the roots seems to be related not only to a decrease in sulfate availability, but also to a transient activation of sulfate translocation making shoots less sensitive to sulfate deficiency (Figure 4B) . Noticeably, Cd exposure neither decreases root sulfate content (Figure 3C) nor inhibits root sulfate uptake (Figure 2A) and sulfate transporter gene expression (Figure 2C), but rather significantly enhances sulfate translocation (Figure 4A) and its metabolism as shown by the significant increases in the GSH levels of the shoot (Figure 3B). Such an effect should be related to the activation of both PC biosynthesis and mechanisms involved in controlling oxidative damage due to the accumulation of free Cd ions in the leaves [47, 48]. Moreover, from these results we can also speculate that the over-accumulation of GSH in the shoot could help roots in detoxifying Cd through reallocating mechanisms involving phloem translocation, as previously reported in other species [49, 50]. In this way, the excess of sulfate taken up by roots would partly bypass root assimilation to be directly metabolized in organs less affected by Cd stress, without however affecting the root sulfate pool (Figure 3C).
Taken as a whole our data clearly show that dissimilar nutritional and metabolic states may result in quite similar responses in sulfate uptake, suggesting that multi-signalling pathways may control the expression of the high-affinity sulfate transporters of the roots. Moreover, the fact that the negative relationships between the levels of nutritional signals (sulfate and GSH) and sulfate uptake capacity of the roots, existing in sulfur-starved plants, are not found in the Cd exposed ones, seems to further support this conclusion.
Although it is difficult to indicate unambiguous nutritional signals, we can make some educated guesses on the general structure of the hypothetical signaling pathways involved in the modulation of sulfate uptake by analyzing the expression pattern of the three BjSultr1;2 forms under Cd exposure and sulfate limitation. Since BjSultr1;2a seems to have lost its capacity to respond to Cd stress, but, at the same time, retains its response to sulfate shortage, we can speculate about the existence of at least two distinct signal transduction pathways. The first one modulates root sulfate uptake, ensuring adequate nutrient supply when plants experience lowering in the sulfate concentration of the soil solution, probably through a cis-acting sulfur responsive element as previously suggested , whilst the second one we postulate is likely to be involved in meeting sulfate uptake with the plant metabolic sulfur demand, which may increase following heavy-metal stress. All the three BjSultr1;2 forms are controlled by the first pathway as indicated by the analysis of their respective contribution to the increase in the cumulative amount of the BjSultr1;2 transcripts under sulfur starvation, but only two forms (BjSultr1;2b/c) seem to have retained the ancient characteristic to be controlled by the second regulatory pathway. In this context the differential transcriptional behaviors of the three BjSultr1;2 forms could be explained by hypothesizing the presence of both “cadmium-” and “sulfur-sensitive” regions in the promoter of an ancient Brassica Sultr1;2 form, which – following polyploidization – may have evolved in sub-functionalized forms, whose combined actions result in molecular and physiological responses to Cd exposure and sulfate limitation similar to those known in species with non-redundant genome [8, 9, 15]. If this were not the case an interference of the metal with the signal transduction pathways involved in the regulation of sulfate uptake should be postulated, as suggested in the recent paper of Shahbaz and co-workers , in which they extensively discuss the effect of copper accumulation on sulfur metabolism-related gene expression. However, copper stress in Brassica seems to produce significant increases in both sulfate uptake and tissue sulfate content without substantially altering plant sulfur demand , differently from Cd exposure which produces increases in sulfate uptake closely related to the strength of the additional sink for thiols it induces (Additional file 11). Moreover, if any sort of Cd interference occurs we should also suppose the existence of at least two signal transduction pathways controlling the expression of BjSultr1;2a/b/c under Cd exposure: the first inhibited by Cd, and the second Cd insensitive. Finally, we cannot exclude that other molecular mechanisms may be involved in the differential expression of the three BjSultr1;2 forms under Cd stress, as for instance those suggested for rice phosphate transporters ; it could be interesting to investigate if the short 9 bp-insertion located at the 5′ end of the BjSultr1;2a coding sequence (Additional file 8) can play a role in the regulation of its expression.
Taken as a whole our data agree with the main molecular and physiological evidence obtained in Arabidopsis which support the idea that the regulation of AtSultr1;1 and AtSultr1;2 – the two transporters mediating sulfate uptake from the soil solution – must necessarily involve independent signaling pathways, as extensively shown by Rouached and co-workers [15, 54]. Moreover, we can also conclude that different sulfur nutritional and metabolic conditions may be perceived by a single sulfate transporter gene. Such a finding reveals that the mechanisms involved in sulfate uptake regulation may be more complex than previously thought, and partially accounts for the lack of unambiguous nutritional signals, since the activity of each transporter may result from a complex interplay among multiple regulatory pathways.
Inductively coupled plasma-mass spectrometry
Open reading frame
Polymerase chain reaction
Reverse transcription - PCR
Standard error of the mean.
This work was supported by the Italian Ministry of Education, University, and Research - PRIN 2009. We would like to thank Alessandro Ferri for its precious support during the revision of the manuscript.
- Leustek T, Martin MN, Bick JA, Davies JP: Pathways and regulation of sulfur metabolism revealed through molecular and genetic studies. Annu Rev Plant Phys. 2000, 51: 141-165. 10.1146/annurev.arplant.51.1.141.View ArticleGoogle Scholar
- Takahashi H, Kopriva S, Giordano M, Saito K, Hell R: Sulfur assimilation in photosynthetic organisms: molecular functions and regulations of transporters and assimilatory enzymes. Annu Rev Plant Biol. 2011, 62: 157-184. 10.1146/annurev-arplant-042110-103921.View ArticlePubMedGoogle Scholar
- Cram W, Rennenberg H, Brunold C, De Kok LJ, Stulen I: Uptake and transport of sulfate. Sulfur Nutrition and Sulfur Assimilation in Higher Plants: Fundamental, Environmental and Agricultural Aspects. The Hague: SPB Academic Publishing, 1990:3-11.Google Scholar
- Clarkson D, Hawkesford M, Davidian J-C: Membrane and long-distance transport of sulfate. Sulfur Nutrition and Sulfur Assimilation in Higher Plants: Fundamental, Environmental and Agricultural Aspects. Edited by: De Kok LJ, Stulen I, Rennenberg H, Brunold C, Rauser WE. 1993, The Hague: SPB Academic Publishing, 3-19.Google Scholar
- Saito K: Sulfur assimilatory metabolism. The long and smelling road. Plant Physiol. 2004, 136: 2443-2450. 10.1104/pp.104.046755.PubMed CentralView ArticlePubMedGoogle Scholar
- Rausch T, Wachter A: Sulfur metabolism: a versatile platform for launching defence operations. Trends Plant Sci. 2005, 10: 503-509. 10.1016/j.tplants.2005.08.006.View ArticlePubMedGoogle Scholar
- Lee S, Leustek T: The effect of cadmium on sulfate assimilation enzymes in Brassica juncea. Plant Sci. 1999, 141: 201-207. 10.1016/S0168-9452(98)00231-3.View ArticleGoogle Scholar
- Nocito FF, Pirovano L, Cocucci M, Sacchi GA: Cadmium-induced sulfate uptake in maize roots. Plant Physiol. 2002, 129: 1872-1879. 10.1104/pp.002659.PubMed CentralView ArticlePubMedGoogle Scholar
- Nocito FF, Lancilli C, Crema B, Fourcroy P, Davidian J-C, Sacchi GA: Heavy metal stress and sulfate uptake in maize roots. Plant Physiol. 2006, 141: 1138-1148. 10.1104/pp.105.076240.PubMed CentralView ArticlePubMedGoogle Scholar
- Nocito FF, Espen L, Crema B, Cocucci M, Sacchi GA: Cadmium induces acidosis in maize root cells. New Phytol. 2008, 179: 700-711. 10.1111/j.1469-8137.2008.02509.x.View ArticlePubMedGoogle Scholar
- Noctor G, Mhamdi A, Chaouch S, Han Y, Neukermans J, Marquez-Garcia B, Queval G, Foyer CH: Glutathione in plants: an integrated overview. Plant Cell Environ. 2012, 35: 454-484. 10.1111/j.1365-3040.2011.02400.x.View ArticlePubMedGoogle Scholar
- Lappartient AG, Touraine B: Demand-driven control of root ATP sulfurylase activity and SO42- uptake in intact canola. The role of phloem-translocated glutathione. Plant Physiol. 1996, 111: 147-157.PubMed CentralPubMedGoogle Scholar
- Lappartient AG, Vidmar JJ, Leustek T, Glass ADM, Touraine B: Inter-organ signaling in plants: regulation of ATP sulfurylase and sulfate transporter genes expression in roots mediated by phloem-translocated compound. Plant J. 1999, 18: 89-95. 10.1046/j.1365-313X.1999.00416.x.View ArticlePubMedGoogle Scholar
- Davidian J-C, Kopriva S: Regulation of sulfate uptake and assimilation - the same or not the same?. Mol Plant. 2010, 3: 314-325. 10.1093/mp/ssq001.View ArticlePubMedGoogle Scholar
- Rouached H, Wirtz M, Alary R, Hell R, Arpat AB, Davidian J-C, Fourcroy P, Berthomieu P: Differential regulation of the expression of two high-affinity sulfate transporters, SULTR1.1 and SULTR1.2, in Arabidopsis. Plant Physiol. 2008, 147: 897-911. 10.1104/pp.108.118612.PubMed CentralView ArticlePubMedGoogle Scholar
- Hawkesford MJ: Plant responses to sulphur deficiency and the genetic manipulation of sulphate transporters to improve S-utilization efficiency. J Exp Bot. 2000, 51: 131-138. 10.1093/jexbot/51.342.131.View ArticlePubMedGoogle Scholar
- Jobe TO, Sung D-Y, Akmakjian G, Pham A, Komives EA, Mendoza-Cózatl DG, Schroeder JI: Feedback inhibition by thiols outranks glutathione depletion: a luciferase-based screen reveals glutathione-deficient γ-ECS and glutathione synthetase mutants impaired in cadmium-induced sulfate assimilation. Plant J. 2012, 70: 783-795. 10.1111/j.1365-313X.2012.04924.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Buchner P, Prosser IM, Hawkesford MJ: Phylogeny and expression of paralogous and orthologous sulphate transporter genes in diploid and hexaploid wheats. Genome. 2004, 47: 526-534. 10.1139/g04-011.View ArticlePubMedGoogle Scholar
- Maruyama-Nakashita A, Nakamura Y, Watanabe-Takahashi A, Inoue E, Yamaya T, Takahashi H: Identification of a novel cis-acting element conferring sulfur deficiency response in Arabidopsis roots. Plant J. 2005, 42: 305-314. 10.1111/j.1365-313X.2005.02363.x.View ArticlePubMedGoogle Scholar
- Maruyama-Nakashita A, Nakamura Y, Tohge T, Saito K, Takahashi H: Arabidopsis SLIM1 is a central transcriptional regulator of plant sulfur response and metabolism. Plant Cell. 2006, 18: 3235-3251. 10.1105/tpc.106.046458.PubMed CentralView ArticlePubMedGoogle Scholar
- Lysak MA, Koch MA, Pecinka A, Schubert I: Chromosome triplication found across the tribe Brassiceae. Genome Res. 2005, 15: 516-525. 10.1101/gr.3531105.PubMed CentralView ArticlePubMedGoogle Scholar
- Lysak MA, Cheung K, Kitschke M, Bureš P: Ancestral chromosomal blocks are triplicated in Brassiceae species with varying chromosome number and genome size. Plant Physiol. 2007, 145: 402-410. 10.1104/pp.107.104380.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang X, Wang H, Wang J, Sun R, Wu J, Liu S, Bai Y, Mun JH, Bancroft I, Cheng F, Huang S, Li X, Hua W, Wang J, Wang X, Freeling M, Pires JC, Paterson AH, Chalhoub B, Wang B, Hayward A, Sharpe AG, Park B-S, Weisshaar B, Liu B, Li B, Liu B, Tong C, Song C, Duran C, et al: The genome of the mesopolyploid crop species Brassica rapa. Nature Genet. 2011, 43: 1035-1039. 10.1038/ng.919.View ArticlePubMedGoogle Scholar
- U N: Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization. Jpn J Bot. 1935, 7: 389-452.Google Scholar
- Lynch M, Force A: The probability of duplicate gene preservation by subfunctionalization. Genetics. 2000, 154: 459-473.PubMed CentralPubMedGoogle Scholar
- He X, Zhang J: Rapid subfunctionalization accompanied by prolonged and substantial neofunctionalization in duplicate gene evolution. Genetics. 2005, 169: 1157-1164. 10.1534/genetics.104.037051.PubMed CentralView ArticlePubMedGoogle Scholar
- Rauser WE: Compartmental efflux analysis and removal of extracellular cadmium from roots. Plant Physiol. 1987, 85: 62-65. 10.1104/pp.85.1.62.PubMed CentralView ArticlePubMedGoogle Scholar
- Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011, 28: 2731-2739. 10.1093/molbev/msr121.PubMed CentralView ArticlePubMedGoogle Scholar
- Schneider CA, Rasband WS, Eliceiri KW: NIH Image to ImageJ: 25 years of image analysis. Nat Methods. 2012, 9: 671-675. 10.1038/nmeth.2089.View ArticlePubMedGoogle Scholar
- Hamilton R, Watanabe CK, de Boer HA: Compilation and comparison of the sequence context around the AUG startcodons in Saccharomyces cerevisiae mRNAs. Nucleic Acids Res. 1987, 15: 3581-3593. 10.1093/nar/15.8.3581.PubMed CentralView ArticlePubMedGoogle Scholar
- Cherest H, Davidian JC, Thomas D, Benes V, Ansorge W, Surdin-Kerjan Y: Molecular characterization of two high affinity sulfate transporters in Saccharomyces cerevisiae. Genetics. 1997, 145: 627-635.PubMed CentralPubMedGoogle Scholar
- Gietz D, Jean AS, Woods RA, Schiestl RH: Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Res. 1992, 20: 1425-10.1093/nar/20.6.1425.PubMed CentralView ArticlePubMedGoogle Scholar
- Cherest H, Surdin-Kerjan Y: Genetic analysis of a new mutation conferring cysteine auxotrophy in Saccharomyces cerevisiae: updating of the sulfur metabolism pathway. Genetics. 1992, 130: 51-58.PubMed CentralPubMedGoogle Scholar
- Tabatabai MA, Bremner JM: A simple turbidimetric method of determining total sulfur in plant material. Agron J. 1970, 62: 805-806. 10.2134/agronj1970.00021962006200060038x.View ArticleGoogle Scholar
- Nocito FF, Lancilli C, Dendena B, Lucchini G, Sacchi GA: Cadmium retention in rice roots is influenced by cadmium availability, chelation and translocation. Plant Cell Environ. 2011, 34: 994-1008. 10.1111/j.1365-3040.2011.02299.x.View ArticlePubMedGoogle Scholar
- Griffith OW: Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal Biochem. 1980, 106: 207-212. 10.1016/0003-2697(80)90139-6.View ArticlePubMedGoogle Scholar
- Hawkesford MJ: Transporter gene families in plants: the sulphate transporter gene family - redundancy or specialization?. Physiol Plantarum. 2003, 117: 155-163. 10.1034/j.1399-3054.2003.00034.x.View ArticleGoogle Scholar
- Hawkesford MJ, De Kok LJ: Managing sulphur metabolism in plants. Plant Cell Environ. 2006, 29: 382-395. 10.1111/j.1365-3040.2005.01470.x.View ArticlePubMedGoogle Scholar
- Takahashi H, Buchner P, Yoshimoto N, Hawkesford MJ, Shiu S-H: Evolutionary relationships and functional diversity of plant sulfate transporters. Front Plant Sci. 2012, 2: 119-10.5923/j.fs.20120205.04.PubMed CentralView ArticlePubMedGoogle Scholar
- Pradhan AK, Pental D: Genetics of Brassica juncea. Genetics and Genomics of the Brassicaceae. Edited by: Bancroft I, Schmidt R. 2011, New York Dordrecht Heidelberg London: Springer, 323-345.View ArticleGoogle Scholar
- Smith FW, Ealing PM, Hawkesford MJ, Clarkson DT: Plant members of a family of sulfate transporters reveal functional subtypes. P Natl Acad Sci USA. 1995, 92: 9373-9377. 10.1073/pnas.92.20.9373.View ArticleGoogle Scholar
- Smith FW, Hawkesford MJ, Ealing PM, Clarkson DT, Vanden Berg PJ, Belcher AR, Warrilow AGS: Regulation of expression of a cDNA from barley roots encoding a high affinity sulphate transporter. Plant J. 1997, 12: 875-884. 10.1046/j.1365-313X.1997.12040875.x.View ArticlePubMedGoogle Scholar
- Takahashi H, Watanabe-Takahashi A, Smith FW, Blake-Kalff M, Hawkesford MJ, Saito K: The roles of three functional sulphate transporters involved in uptake and translocation of sulphate in Arabidopsis thaliana. Plant J. 2000, 23: 171-182. 10.1046/j.1365-313x.2000.00768.x.View ArticlePubMedGoogle Scholar
- Yoshimoto N, Takahashi H, Smith FW, Yamaya T, Saito K: Two distinct high-affinity sulfate transporters with different inducibilities mediate uptake of sulfate in Arabidopsis roots. Plant J. 2002, 29: 465-473. 10.1046/j.0960-7412.2001.01231.x.View ArticlePubMedGoogle Scholar
- Yoshimoto N, Inoue E, Watanabe-Takahashi A, Saito K, Takahashi H: Posttranscriptional regulation of high-affinity sulfate transporters in Arabidopsis by sulfur nutrition. Plant Physiol. 2007, 145: 378-388. 10.1104/pp.107.105742.PubMed CentralView ArticlePubMedGoogle Scholar
- Kataoka T, Hayashi N, Yamaya T, Takahashi H: Root-to-shoot transport of sulfate in Arabidopsis. Evidence for the role of SULTR3;5 as a component of low-affinity sulfate transport system in the root vasculature. Plant Physiol. 2004, 136: 4198-4204. 10.1104/pp.104.045625.PubMed CentralView ArticlePubMedGoogle Scholar
- Nocito FF, Lancilli C, Giacomini B, Sacchi GA: Sulfur metabolism and cadmium stress in higher plants. Plant Stress. 2007, 1: 142-156.Google Scholar
- Jozefczak M, Remans T, Vangronsveld J, Cuypers A: Glutathione is a key player in metal-induced oxidative stress defenses. Int J Mol Sci. 2012, 13: 3145-3175. 10.3390/ijms13033145.PubMed CentralView ArticlePubMedGoogle Scholar
- Mendoza-Cózatl DG, Jobe TO, Hauser F, Schroeder JI: Long-distance transport, vacuolar sequestration, tolerance, and transcriptional responses induced by cadmium and arsenic. Curr Opin Plant Biol. 2011, 14: 554-562. 10.1016/j.pbi.2011.07.004.PubMed CentralView ArticlePubMedGoogle Scholar
- Li Y, Dankher OP, Carreira L, Smith AP, Meaghe RB: The shoot-specific expression of γ-glutamylcysteine synthetase directs the long-distance transport of thiol-peptides to roots conferring tolerance to mercury and arsenic. Plant Physiol. 2006, 141: 288-298. 10.1104/pp.105.074815.PubMed CentralView ArticlePubMedGoogle Scholar
- Shahbaz M, Stuiver CEE, Posthumus FS, Parmar S, Hawkesford MJ, De Kok LJ: Copper toxicity in Chinese cabbage is not influenced by plant sulphur status, but affects sulphur metabolism-related gene expression and the suggested regulatory metabolites. Plant Biology. 2014, 16: 68-78. 10.1111/plb.12019.View ArticlePubMedGoogle Scholar
- Shahbaz M, Tseng MH, Stuiver CEE, Koralewska A, Posthumus FS, Venema JH, Saroj P, Schat H, Hawkesford MJ, De Kok LJ: Copper exposure interferes with the regulation of the uptake, distribution and metabolism of sulfate in Chinese cabbage. J Plant Physiol. 2010, 167: 438-446. 10.1016/j.jplph.2009.10.016.View ArticlePubMedGoogle Scholar
- Secco D, Baumann A, Poirier Y: Characterization of the rice PHO1 gene family reveals a key role for OsPHO1;2 in phosphate homeostasis and the evolution of a distinct clade in dicotyledons. Plant Physiol. 2010, 152: 1693-1704. 10.1104/pp.109.149872.PubMed CentralView ArticlePubMedGoogle Scholar
- Rouached H, Secco D, Bulak Arpat A: Getting the most sulfate from soil: regulation of sulfate uptake transporters in Arabidopsis. J Plant Physiol. 2009, 166: 893-902. 10.1016/j.jplph.2009.02.016.View ArticlePubMedGoogle Scholar
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