Abstract
Variable environmental availability of metal ions represents a constant challenge for most organisms, so that during evolution, they have optimised physiological and molecular mechanisms to cope with this particular requirement. Metallothioneins (MTs) are proteins that play a major role in metal homeostasis and as a reservoir. The MT gene/protein systems of terrestrial helicid snails are an invaluable model for the study of metal-binding features and MT isoform-specific functionality of these proteins. In the present study, we characterised three paralogous MT isogenes and their expressed products in the escargot (Cantareus aspersus). The metal-dependent transcriptional activation of the three isogenes was assessed using quantitative Real Time PCR. The metal-binding capacities of the three isoforms were studied by characterising the purified native complexes. All the data were analysed in relation to the trace element status of the animals after metal feeding. Two of the three C. aspersus MT (CaMT) isoforms appeared to be metal-specific, (CaCdMT and CaCuMT, for cadmium and copper respectively). A third isoform (CaCd/CuMT) was non-specific, since it was natively recovered as a mixed Cd/Cu complex. A specific role in Cd detoxification for CaCdMT was revealed, with a 80–90% contribution to the Cd balance in snails exposed to this metal. Conclusive data were also obtained for the CaCuMT isoform, which is involved in Cu homeostasis, sharing about 30–50% of the Cu balance of C. aspersus. No apparent metal-related physiological function was found for the third isoform (CaCd/CuMT), so its contribution to the metal balance of the escargot may be, if at all, of only marginal significance, but may enclose a major interest in evolutionary studies.
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Introduction
Fluctuating environmental availability of metallic trace elements represents a constant challenge for most organisms, which have to activate regulatory mechanisms to adjust and keep their internal trace element status within a physiologically tolerable range. This holds even more so because certain metal ions exert toxic effects at even very low concentrations, whereas other metals that are essential constituents of biomolecules cause adverse effects at high concentrations. Proteins playing an accommodating role in respect to these contrasting impacts are the so-called Metallothioneins (MTs). They belong to a ubiquitous, heterogeneous family of proteins with the ability to bind closed-shell metal ions via the sulphur atoms of their cysteine residues (Kägi and Kojima 1987; Sigel et al. 2009; Blindauer and Leszczyszyn 2010). In no animal group other than pulmonate molluscs, evolutionary differentiation brought about MT isoforms that possess such a strictly exclusive, sequence-based metal specificity (Palacios et al. 2011) being involved in contrasting metal-specific tasks such as cadmium detoxification, on the one hand, and homeostatic copper regulation, on the other (Dallinger et al. 1997). Hence, a number of pulmonate species has so far been shown to respond to environmental Cd exposure by synthesising an MT isoform loaded with high amounts of Cd (Dallinger et al. 1989). Its amino acid sequence has been elucidated for several species, including the Roman snail, Helix pomatia (Dallinger et al. 1993), the copse snail, Arianta arbustorum (Berger et al. 1995), and the escargot, Cantareus aspersus (Hispard et al. 2008). In accordance with its tissue-specific synthesis in digestive and excretory organs (Chabicovsky et al. 2003) and because of its protective effect against Cd, its function has been assigned to the detoxification of this metal ion (Manzl et al. 2004), and it was thus named CdMT. In contrast, a second MT type of isoforms, almost exclusively associated with Cu, have been characterised and named CuMTs (Dallinger et al. 1997). These are synthesised exclusively in the so-called rhogocytes, a specific molluscan cell type in which haemocyanin, the Cu-bearing respiratory pigment of snails, is synthesised (Chabicovsky et al. 2003). Consequently, a predominantly homeostatic function in connection with the supply of Cu for haemocyanin synthesis has been suggested (Dallinger et al. 2005). Recently, a third isoform was identified, first in C. aspersus (Hispard et al. 2008; Schuler et al. 2008) and then in other snail species (Palacios et al. 2011). This isoform exhibits no definite metal-specificity, since it was isolated from the midgut gland of Cd-exposed snails as a complex including both Cd and Cu, and was therefore named Cd/CuMT. Interestingly, the three MT protein sequences differ only in some of their non-Cys residues, signifying that these amino acids must be crucial in determining metal specificity of each isoform (Schuler et al. 2008; Palacios et al. 2011).
In the present work, we examine the role of the three MT isoforms in the accumulation and partitioning of metal ions (Cd2+, Zn2+, and Cu+) in pulmonate tissues, using the edible snail, C. aspersus (the so-called escargot), as a study object. C. aspersus is one of the most common terrestrial pulmonate species, with an original distribution in Southern and Western Europe (Kerney and Cameron 1979) but nowadays widespread in many parts of the world owing to anthropochorous spreading (Guiller and Madec 2010). The significance of C. aspersus lies in its ecological impact for nutrient fluxes in the soil (Dallinger et al. 2001). Moreover, this species has been known as a pest organism in horticulture (Godan 1979) while at the same time being appreciated as the “edible snail” in gastronomy (Chevallier 1983). Therefore, a global acknowledgement of the biochemistry and physiology of metal uptake and regulation in this species is of general interest. This goal has been tackled here using different experimental approaches. Long-term metal exposure experiments yielded information about metal accumulation in the snail midgut gland and differential patterns of transcriptional induction for the three isogenes, depending on the metal surplus (Cd and Cu) applied. The three isoforms were purified and their metal load analysed quantitatively. In addition, their metal-binding abilities were assessed by mass spectrometric analysis of the respective metal complexes obtained by recombinant synthesis in metal-supplemented E. coli cultures. Our data reveal that each of the three MT isoforms contributes specifically and differentially to the metal status in snail tissues, confirming the adaptational significance of the snail MT system for coping with different trace element availabilities under fluctuating (rapidly changing) environmental conditions.
Materials and methods
Animals and rearing conditions for control and metal exposure studies
Cantareus aspersus snails were from laboratory strains of the Department of Chrono-Environment of the University of Franche-Comté (Besançon, France). About 120 individuals were kept in plastic boxes on garden soil complemented with lime powder (CaCO3) at 18°C and with a photoperiod of 12:12 h. Snails were fed every third day with commercially available lettuce (Lactuca sativa). For metal enrichment, lettuce leaves were soaked for 1 h in Titrisol standard dilutions of CdCl2 or CuCl2 (Merck, Darmstadt, Germany) made up to concentrations of 1 mg Cd2+ l−1 and 3 mg Cu2+ l−1, respectively. Resulting concentrations of Cd and Cu in metal-enriched and untreated lettuce are summarised in Table 1. Another 35 individuals were fed on lettuce supplemented with Cd2+ or Cu2+. Additionally, 40 animals fed on untreated lettuce were used as controls. On day 0, five individuals of the control group, and on days 1, 2, 3, 5, 8, 14, and 29, five snails of each group (control, Cd2+ and Cu2+-exposed) were sampled for RNA isolation and tissue metal analyses. Finally, for MT protein purification, two groups of 30 animals each were kept in large plastic boxes and fed for 2 weeks either with uncontaminated (control diet) or Cd-enriched lettuce leaves prepared as described above. At the end of the feeding period, all snails were sacrificed by decapitation and processed for protein purification and characterisation.
RNA isolation and reverse transcription
After dissection, ~10 mg (fresh weight) of midgut gland tissue from each individual were removed for RNA isolation, whilst the remaining midgut gland and foot tissue were used to determine Cd and Cu concentrations as described below. Individual midgut gland aliquots were homogenised (Ultra Turrax T25, IKA, Staufen, Germany) in TRIzol® reagent and RNA was subsequently isolated according to a standard protocol (Sigma, Taufkirchen, Germany). The RiboGreen® RNA Quantitation Kit from Molecular Probes (Invitrogen, Karlsruhe, Germany) was used for quantification after DNase I (Fermentas, St. Leon-Rot, Germany) digestion. 450 ng of RNA per individual were subjected to cDNA synthesis (RevertAid™ H Minus M-MuLV Reverse Transcriptase, Fermentas) for subsequent isoform-specific PCR and quantitative Real Time PCR.
PCR amplification, cloning and sequencing of the cDNA of the MT isogenes
For amplification of Cd- and CuMT cDNAs, the following specific primers, designed after the H. pomatia orthologous sequences (Dallinger et al. 2004), were used:
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CdMT-S: 5′-CTC CAT GGC AAC CAT GAG CGG AAA-3′
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CdMT-AS: 5′-GCG TCG ACT TGT CCT GCG GTT ACT-3′
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CuMT-S: 5′-GTG ACC GAT GCA GTT CTT GCC ATT-3′
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CuMT-AS: 5′-GCG TCG ACT TGT CGT TTA TTT GCA G-3′
PCR conditions were as follows: first denaturation at 94°C for 2 min, 39 cycles at 94°C for 20 s, 55°C for 10 s, 65°C for 40 s, and a final extension at 65°C for 10 min. Amplification of the CdMT cDNA from C. aspersus generated two PCR products of the same length, which, after cloning and sequencing, were distinguished as CdMT cDNA and Cd/CuMT cDNA. The SMART™ RACE cDNA Amplification Kit (Clontech Laboratories) was used for completion of both cDNA sequences. PCR products were cloned into pCR®4 vector (TOPO TA Cloning® Kit for Sequencing from Invitrogen) and sequenced using an AB 3130 genetic analyser (BigDye Terminator v3.1 Sequencing Kit, AB). Primer sequences for RACE PCR were as follows:
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CdMT3-R-S: 5′-CAG GAG CGA GCC TTG CCA GTG TGG GAG-3′
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CdMT5-R-AS: 5′-GCA AGT CTT GCA GGC GGC ACA TGT-3′
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CuMT-3-R-S: 5′-TGT GAC CGA TGC AGT TCT TGC CAT TGT TCC-3′
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CuMT-5-R-AS: 5′-ACT GCC ACA TTT GCA TGA TCC ACT TCC GGT-3′
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CuMT-3-R (NGSP) S: 5′-TGA CGA CTG CAA GTG TGG TAG CCA ATG-3′
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Cd/CuMT-3-R-S: 5′-CTA CTC CTG CCA ATG CAA CAA TGA CAC C-3′
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Cd/CuMT 5-R AS: 5′-CCA GTG CGG CTA TGG GAG AGA GTG GTG A-3′
Touchdown PCR was performed using Advantage 2 polymerase (Clontech) with cycling parameters as follows: 5 cycles at 94°C for 30 s and 72°C for 3 min; 5 cycles at 94°C for 30 s, 70°C for 30 s, 72°C for 3 min; 30 cycles at 94°C for 30 s, 68°C for 30 s, 72°C for 3 min. Nested PCR was applied to amplify the CuMT cDNA using the following conditions: 39 cycles at 94°C for 30 s, 68°C for 30 s, 72°C for 3 min and a final extension at 72°C for 10 min. NGSP (see above) stands for nested gene specific primer.
Quantitative Real Time PCR
Quantitative Real Time PCR for the Cd-, Cu-, and Cd/CuMT cDNAs was performed on a 7500 Real Time PCR analyser (Applied Biosystems, Foster City, CA, USA) using Power SYBR Green. Amplicon plasmids were used to generate calibration curves for copy number analysis of ∆ct values for each isogene. Primers were designed with Primer Express 3.0 software (Applied Biosystems). Dissociation curves were used to elucidate the optimal primer concentrations. 2 μl cDNA were applied for Real Time detection PCR in a 20 μl approach (1× Power SYBR Green PCR Mastermix, 1× U-BSA, sense-, antisense primer). All transcripts had specific amplicon lengths (CdMT: 56 bp; CuMT: 74 bp; Cd/CuMT: 59 bp) and were amplified using the following concentrations and primers:
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Cd-MTCa sense, 300 nM: 5’-GCC GCC TGT AAG ACT TGC A-3’;
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Cd-MTCa antisense, 900 nM: 5’-CAC GCC TTG CCA CAC TTG-3’.
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Cu-MTCa sense, 900 nM: 5’-AAC AGC AAC CCT TGC AAC TGT-3’
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Cu-MTCa antisense, 900 nM: 5’-CGA GCA CTG CAT TGA TCA CAA-3’
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CdCu-MT sense, 900 nM: 5’-TGT GGA GCC GGC TGT TCT-3’
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CdCu-MT antisense, 300 nM: 5’-CAG GTG TCA TTG TTG CAT TGG-3’
Metal analysis
Cd and Cu concentrations in midgut gland tissues (samples taken on days 0, 3, 5, 8, 14, and 29) of each individual as well as in lettuce leaf aliquots were determined by flame atomic absorption spectrophotometry (AAS). After sample drying at 60°C and weight determination, digestion was achieved in 12 ml screw-capped polyethylene tubes (Greiner, Austria) with a mixture (1:1) of nitric acid (suprapure, Merck, Darmstadt, Germany) and deionised water in a heated aluminium digestion oven at 70°C until a clear solution was obtained. The samples were diluted to 11.5 ml with deionised water. Cd and Cu concentrations were measured in the flame of an atomic absorption instrument (model 2380, Perkin Elmer, Boston, MA, USA).
Purification of native MT isoforms by standard chromatography and HPLC
After the 14-day exposure treatment (see above), midgut glands of control and Cd-exposed snails were pooled from five animals each and processed immediately for chromatography or otherwise stored at −80°C until further use. Pooled midgut gland samples (~3.0–3.5 g fresh weight) were homogenised in a threefold volume (v/w) of 25 mM Tris HCl buffer (pH 7.5) to which 100 mM NaCl, 5 mM 2-mercaptoethanol (Merck), and 0.1 mM phenylmethylsulfonyl fluoride (Merck) had been added. Homogenates were centrifuged for 1 h at 27,000×g in a high speed centrifuge (model RC 5C, Sorvall Instruments, Golden Valley, MN, USA). Resulting supernatants were purified in a step by step procedure by DEAE (diethylaminoethyl) cellulose extraction, gel permeation chromatography, ultrafiltration and reversed phase high performance liquid chromatography (RP-HPLC) (Berger et al. 1997). For gel permeation chromatography, samples were split into 6-ml aliquots and applied successively to a column (15 × 300 mm) packed with Sephacryl S-100 (GE Healthcare Europe GmbH, Munich, Germany), calibrated with a mixture of Blue Dextran (2000 kDa), chicken egg albumin (45 kDa), myoglobin (18.5 kDa), and vitamin B12 (1.35 kDa). After chromatography, metal concentrations (Cd, Cu and Zn) were measured in fractions by AAS and the presumed MT-containing fractions were pooled and concentrated by ultrafiltration (Amicon YM1, Beverly, MA, USA; 1 kDa cut-off). Subsequently, samples were further fractionated on an HPLC system (model 501, Waters, Milford, LA, USA) equipped with a multi-wavelength detector (model 490E; Waters), using a μBondapack C18 column (Waters). Elution was performed in a Tris HCl/acetonitrile gradient over 35 min (Hispard et al. 2008). Fractions were diluted with deionised water and analysed for metal concentrations (Cd, Zn, Cu) as described above.
Recombinant synthesis and purification of the metal-MT complexes
The cDNAs encoding each of the three C. aspersus isoforms, isolated as described in the previous section, were subcloned in the pGEX expression vector for recombinant synthesis of the corresponding proteins in E. coli BL21 cells, essentially as described for the H. pomatia MT isoforms (Palacios et al. 2011). Recombinant synthesis of CdMT, CuMT and Cd/CuMT was performed in metal supplemented LB medium (300 μM CdCl2 or 500 μM CuSO4), which allows the recovery of in vivo folded metal-MT complexes. Full analysis of all recombinant metal complexes of C. aspersus MT isoforms will be provided in a forthcoming publication.
Mass spectrometry analysis of recombinant metal-CaMT complexes
Molecular mass determination was performed by electrospray ionisation mass spectrometry equipped with a time-of-flight analyser (ESI-TOF MS) using a Micro Tof-Q Instrument, Bruker Daltonics Gmbh (Bremen, Germany) calibrated with NaI (200 ppm NaI in a 1:1 H2O: isopropanol mixture), interfaced with a Series 1100 HPLC pump (Agilent Technologies) equipped with an autosampler, both controlled by the Compass Software. The experimental conditions for analysing proteins with Cd were: 20 μl of the sample were injected through a long PEEK tube (1.5 m × 0.18 mm i.d.) at 40 μl/min under the following conditions: capillary-counter-electrode voltage, 5.0 kV; desolvation temperature, 90–110°C; dry gas, 6 l/min. Spectra were collected throughout an m/z range from 800 to 2000. The proteins containing copper were analysed by injecting 20 μl of the 30 μl/min sample; capillary-counter-electrode voltage, 4.0 kV; desolvation temperature, 80°C; m/z range from 800 to 2000. The liquid carrier was a 90:10 mixture of 15 mM ammonium acetate and acetonitrile, pH 7.0. All samples were injected at least in duplicate to ensure reproducibility. In all cases, molecular masses were calculated according to the method reported by Fabris et al. (1996).
Statistics
Statistical analyses were performed using the software packages Statistica (version 8; StatSoft Inc., Tulsa, OK, USA) and Sigma Plot (version 11; Systat Software Inc., Chicago, IL, USA). Real Time PCR plots were tested by analysis of variance (ANOVA). In addition, differences between single values of different treatments (Cd or Cu-exposed versus controls) were analysed by means of the Mann–Whitney rank sum test. A t-test was applied for statistical comparison of Cd and Cu concentrations in midgut gland during metal exposure. In all cases, statistical significance was defined at P ≤ 0.05.
Results and discussion
The three MT isoforms encoded in the C. aspersus genome
Figure 1 shows the amino acid sequences of the three MT isoforms from C. aspersus, as deduced from their respective cDNA sequences (GenBank accession numbers: CaCdMT, ABL73910; CaCuMT, ABM55268; CaCd/CuMT, ABM92276; Palacios et al. 2011). Upon alignment, it became evident that the three proteins share a high degree of similarity, particularly for the highly conserved cysteines and some amino acid positions flanking them. All isoform sequences largely match those of the orthologous MT isoforms in the Roman snail (Helix pomatia) (Fig. 1a), previously isolated and characterised from the midgut gland of H. pomatia (Dallinger et al. 1993, 1997; Berger et al. 1997). The third MT isoform (CaCd/CuMT), first identified in C. aspersus among all snail species (Schuler et al. 2008; Hispard et al. 2008), exhibits a sequence with intermediate peculiarities between those of CaCuMT and CaCdMT (Fig. 1a) and is largely similar to the corresponding isoform in H. pomatia which occurs in two allelic variants (Fig. 1b). It is worth remembering, however, that the designation as CaCd/CuMT has been ascribed to this isoform not from sequence features, but owing to the fact that it is natively recovered as a protein complex including Cd2+ and Cu+ ions simultaneously (Hispard et al. 2008). The occurrence of three MT isoforms with differential metal specificities and functions seems to be an evolutionary hallmark of this mollusc taxon (Palacios et al. 2011). Although it is obvious that all three MT isoforms must interact to maintain a physiological metal balance in their host, their particular contribution to the metal status of snails has so far not been elucidated.
Metal accumulation in C. aspersus snails
In the present study, garden snails were exposed to elevated Cd or Cu levels in the food over a long-term period of 29 days. During this time, metal accumulation and transcriptional activation of the three MT isoforms were assessed in the snail midgut gland, since this organ accounts for most of the short and long-term metal accumulation in pulmonate snails (Dallinger and Wieser 1984; Hispard et al. 2008).
Cd was found steadily enriched in the midgut gland of Cd-exposed animals until the end of the feeding period, reaching maximum concentrations of more than 150 μg/g Cd. At the end of the exposure period, midgut gland Cd concentrations in exposed snails exceeded control levels by a factor of about 30 (Fig. 2a). In contrast to Cd, Cu uptake in the midgut gland of C. aspersus started from a considerably higher concentration level under control conditions (Fig. 2b) showing accumulation rates in metal-exposed individuals that are more restrained when compared to Cd accumulation. This observation coincides well with similar findings in other pulmonate snails (Dallinger and Wieser 1984) and reflects the fact that Cu is an essential trace element which has cellular concentration levels that are, to a certain extent, subject to a regime of intracellular regulation (Dallinger et al. 2005). In fact, significantly increased Cu concentrations were reached in the midgut gland of exposed snails only towards the end of the long-term feeding period, when Cu concentrations exceeded the respective control levels by a factor of 6 (Fig. 2b).
Transcription regulation of the C. aspersus MT isogenes
The long-term course of mRNA transcription of the CdMT, CuMT and Cd/CuMT genes in C. aspersus varied in an isoform and metal-specific manner, as shown by quantitative Real Time PCR results (Fig. 3). Already under control conditions, the basal mRNA transcription rates differed significantly between the three MT isogenes, showing the highest levels for CdMT, followed by intermediate levels of CaCuMT, and lowest values for CaCd/CuMT (Fig. 3). Results for gene induction are reported and discussed separately for each MT isoform.
Transcription of the CaCdMT gene
Upon Cd exposure, a significant induction of transcription was observed for CaCdMT (Fig. 3a), in contrast to the null response detected for the two other isogenes (Fig. 3b, c). This strong upregulation persisted until day 29, yielding mRNA copy numbers which ranged between 200,000 and 600,000, in contrast to the control group which showed copy numbers below 100,000. Interestingly, the CaCdMT induction rate reached a peak on day 8 of the feeding period (Fig. 3a). This may be due to the fact that at the beginning of Cd exposure, the concentration of free Cd2+ ions able to interact with the gene regulatory regions is higher than at later stages, when an increasing fraction of the metal ion is already bound to the CdMT protein. Overall, the transcriptional response of the CdMT gene in snails appears to proceed more slowly than in mammals, where highest induction peaks are observed few hours after Cd exposure, at least when injecting Cd (Swerdel and Cousins 1982). Furthermore, MT gene induction following intraperitoneal administration of Cd in a marine flatfish peaked in the liver after 4 days, and more rapidly in kidney and gills (George et al. 1996). This indicates that MT gene induction is tissue- and species-dependent, which may reflect differing molecular pathways and agents involved in such mechanisms (Höckner et al. 2009).
Conversely to Cd treatment, there was no induction of the CaCdMT gene by Cu exposure (Fig. 3d). These findings confirm that the CaCdMT gene of C. aspersus is upregulated specifically by Cd, which is consistent with the particularly important role ascribed to the CdMT protein upon Cd uptake through the feed (see below). Apart from its high response towards Cd, it cannot be excluded that CaCdMT may also be responsive to other, non-metallic cellular or environmental stressors, in a similar way that the orthologous gene in H. pomatia also exhibits a slight response towards non-metallic environmental stresses, such as desiccation (Egg et al. 2009).
Transcription of the CaCuMT gene
While there was no response of CaCuMT towards Cd, a slight transcriptional activation of this gene was observed after Cu intake (Fig. 3e). Although in Cu-exposed animals, the trend of transcription pattern over the course of time was not significant upon testing by ANOVA, some particular mRNA concentrations (i.e. those on days 1, 3 and 8) showed significant differences compared to the respective control values. However, in comparison with the strong responsiveness of the CaCdMT gene towards Cd, this occasional upregulation of the CaCuMT gene by Cu must be considered as very weak. Overall, this is consistent with the hypothesis that the main task of the CaCuMT isogene is not Cu detoxification, but rather the physiological homeostasis of this metal ion. In H. pomatia, the mRNA of the homologous gene is exclusively detected in rhogocytes, which are the cells where the Cu-bearing respiration pigment haemocyanin is synthesised. For this reason, HpCuMT has been suggested to serve in Cu donation to the nascent haemocyanin (Dallinger et al. 2005).
Transcription of the CaCd/CuMT gene
As shown by the Real Time PCR results, neither Cd nor Cu exposure induced the CaCd/CuMT gene (Fig. 3c, f). Noteworthy, and as for CuMT, in Cu-exposed snails a few mRNA copy number values appeared to be slightly elevated compared to the respective controls (Fig. 3f). The level of transcriptional activation of the CaCd/CuMT gene was the lowest observed among all three C. aspersus MT genes, which, together with the low rate of constitutive expression, suggests that its contribution to the overall metal balance in this species may be of only marginal significance.
Contribution of MT isoforms to metal binding in C. aspersus: purification of native metal-MT complexes
Midgut gland cytosol fractions of controls and Cd-exposed snails were examined for the presence of MT isoforms and their association with Cd, Cu and Zn. To this end, midgut gland homogenates were first separated into soluble and pellet fractions. The subcellular distribution analysis of Cd, Cu and Zn revealed that Cd was mainly present in the soluble cytosol (80–90%), whereas Cu and Zn were predominantly detected in pellet fractions (Cu: 60–80%; Zn: 80–85%), a distribution that is typical for the midgut gland of terrestrial pulmonate snails (Dallinger and Wieser 1984).
For MT purification, supernatants were consecutively applied to anion exchange and gel permeation chromatography, followed by ultrafiltration and RP-HPLC fractionation. As shown by the elution profiles of the final RP-HPLC step (Fig. 4), the presence of different isoforms, and the partitioning of metals among them, depended on the metal-feeding status of the animals (controls vs. Cd-exposed). Control snails rendered practically one single MT peak showing a high absorption at 254 nm (Fig. 4a). Due to its exclusive Cu load and owing to its elution behaviour in comparison with the HpCuMT isoform (Berger et al. 1997; Dallinger et al. 2005), this peak was attributed to CaCuMT (Fig. 4b). The identification of this sequence as a CaCuMT isoform was corroborated by the fact that, upon recombinant synthesis in E. coli of the corresponding cDNA (Hispard et al. 2008), the resulting protein was a unique, homometallic Cu-loaded complex, a behaviour exhibited only by highly specific Cu-thioneins (Bofill et al. 2009). This isoform was equally detected in Cd-fed snails—without major changes in its abundance, elution time, Cu load, and Cu:Cd:Zn molar ratio (Fig. 4c, d; Table 2). The nearly exclusive Cu content of this isoform, and its independence of the state of Cd accumulation in the snail, corroborates the view that CaCuMT may be involved in the homeostatic regulation of Cu, rather than being responsible for detoxification processes (Dallinger et al. 2005; Hispard et al. 2008). This is in concordance with the observation that the transcription of CaCuMT in the midgut gland of C. aspersus does not vary as a function of supra-physiological exposure to Cd or Cu.
In addition to the CuMT isoform, the Cd-exposed snails exhibited two additional MT peaks that were not present in control animals. Both peaks showed an increased absorption at 254 nm (Fig. 4c) but differed with respect to their metal content (Fig. 4d). One of them was characterised by a clear preponderance of Cd over Cu, with a molar ratio of about 10 Cd:1 Cu and only traces of Zn (Table 2), and owing to this, it was identified as CaCdMT. The ability of this peptide to spontaneously form pure Cd complexes after recombinant expression in Cd-exposed E. coli cells is documented below. Interestingly, a considerable amount of CaCdMT mRNA had been detected in untreated snails (Fig. 3). This raises the question of why CaCdMT was not detectable in control animals at the protein level, in spite of conspicuously elevated basal mRNA concentrations. Several hypotheses could account for this apparent inconsistency, for example, that the lack of protein might be the result of inhibitory post-transcriptional regulatory mechanisms, or that, in the absence of metals, the peptide resulting from translation may be readily proteolysed in the cell, since apoMTs are known to be highly susceptible to degradation (Krezoski et al. 1988).
The second additional MT peak in the elution profile of Cd-exposed snails showed the simultaneous presence of Cd and Cu (Fig. 4d). In fact, due to this mixed metal-binding character, this isoform had been designated as CaCd/CuMT (Schuler et al. 2008; Hispard et al. 2008). The quantitative analysis of its metal content showed that Cd and Cu were present at a molar ratio of about [1 Cu:0.5 Cd], with only traces of Zn (Table 2). Its identity with the expression product of the corresponding gene (CaCd/CuMT) (Fig. 1) was confirmed by recombinant expression of the CaCd/CuMT cDNA in E. coli, which yields an MT peptide exhibiting non-specific metal-binding abilities, a behaviour sharply contrasting with the two metal-specific isoforms, as commented below. It is worth noting that Cd injection in marine crustaceans also yielded MT complexes including both Cd and Cu ions, as shown, for example, in the crab C. pagurus (Overnell and Trewhella 1979). This observation was also related to the special needs of these organisms for Cu.
Compared to MTs from other animal species, the C. aspersus native MT preparations were characterised by their remarkably poor content of Zn, even under physiological conditions (Fig. 4, Table 2) (Gehrig et al. 2000). Already in control snails, Zn was present in minor quantities in midgut gland cytosolic MT fractions and very low amounts, if any, were detectable in MT-containing fractions after gel permeation chromatography. Even less Zn, if at all, could be assessed in any of the three MT isoform peaks purified from Cd-treated snails (Table 2). Interestingly, low content or complete absence of Zn seems to be a consistent feature of pulmonate MTs and may be a consequence of the fact that in pulmonate midgut glands this metal ion is predominantly associated with granular fractions, where it may occur in a chemical form not suitable for MT binding (Dallinger et al. 1989). Therefore, the handling of essential Zn in pulmonate snails does not seem to be mediated primarily by MTs, which is concordant with the inability of Zn2+ to induce any of the three C. aspersus MT isoform genes. As shown before in this study, the snail CdMT isoform is synthesized at low basal levels in the absence of Cd2+, when it may be present as Zn-loaded complexes, hardly detectable because of their low concentration. Most probably they are involved in stress-responsive functions (Egg et al. 2009) and therefore unlikely to play a major role for the Zn status in the snail organism.
Specificity of the metal-binding behaviour of the CaMT isoforms
We have recently shown that the H. pomatia metal-specific isoforms (HpCdMT and HpCuMT) exhibited a sequence-inherent property to form single, homometallic complexes when recombinantly synthesised in bacteria grown in media supplemented with their cognate metal and not vice versa (Palacios et al. 2011). Thus the properties of the metal-MT preparations resulting from recombinant synthesis can be considered an accurate test of MT metal-specificity. Consequently, we first characterised the products of expression of CaCdMT and CaCuMT in E. coli cells grown in cadmium and copper enriched media. In the former case, CaCdMT rendered a unique, homometallic cadmium complex as shown by the single ESI-MS peak of 7486.9 Da (corresponding to a Cd6–CaCdMT complex) (Fig. 5a). In contrast, when recombinantly produced in the presence of Cu, CaCdMT is unable to form homometallic, unique complexes (manuscript in preparation). This is exactly the same result yielded by the orthologous HpCdMT, indicating that this feature of extreme Cd specificity may be shared by all pulmonate snail CdMT isoforms (Palacios et al. 2011).
On the other hand, when the CaCuMT gene was recombinantly expressed in E. coli under Cu surplus, the only recovered product was identified as a homometallic complex with a molecular mass of 7408.3 Da, corresponding to the Cu12-CaCuMT species (Fig. 5b). In contrast, in this case, recombinant synthesis of this isoform with Cd or Zn produced variable mixtures of complexes with different stoichiometries, but never homometallic species (data not shown; manuscript in preparation). These results confirm the exceptional specificity of the CuMT isoform for Cu+, which is also corroborated by its nearly exclusive Cu load when purified from Cd-exposed snails (Table 2). In fact, CaCuMT synthesis is not upregulated by Cu or other metals (Fig. 3b, e), as otherwise would be expected for a protein functioning as a Cu donor for haemocyanin synthesis (Dallinger et al. 2005).
The higher sequence similarity of the CaCd/CuMT isoform with CaCuMT than with CaCdMT (Fig. 1), led to the assumption that CaCd/CuMT and CaCuMT share a common ancestor in pulmonate snail origin (Palacios et al. 2011). A reflection of this close sequence resemblance is that both isoforms are natively recovered as Cu-containing complexes (homometallic or heterometallic) (Fig. 4; Table 2). But CaCd/CuMT is also associated with conspicuous amounts of Cd2+ at a molar ratio of [1 Cu:0.5 Cd] (Table 2), thus, in contrast to the specific CaCuMT isoform, CaCd/CuMT lacks metal specificity, either because it has not yet achieved this property or because it lost it during evolution. Indeed, the nature of the metal complexes formed by this isoform upon its recombinant synthesis under metal exposure indicates that CaCd/CuMT does not exhibit any definite metal specificity, since it gives rise to mixtures of metal:protein species with variable stoichiometries in the presence of either Cd2+ or Cu2+ (shown in Fig. 5c for the former). Furthermore, some of the Cd-species include S2− ligands (Fig. 5c), which is a trait indicative of Cu-thionein character (Capdevila et al. 2005; Bofill et al. 2009; Orihuela et al. 2010). Concordantly, this isoform exhibits intermediate features regarding its induction pattern and synthesis. Hence, the CaCd/CuMT gene is clearly not inducible by metals, showing invariantly and extremely low mRNA levels in either control, Cu or Cd-exposed snails (Fig. 3c, f), reflecting the constitutive expression characteristics of CuMT genes. In contrast to this observation, a protein peak of this isoform was detectable by means of RP-HPLC in Cd-exposed snails (Fig. 4c, d), indicating that its synthesis or its formation may have been induced by the presence of Cd2+. One possible explanation for these contradicting findings may be that in spite of the invariably low CaCd/CuMT mRNA concentration, a certain quantity of this isoform may yet be synthesised in Cd-exposed animals, so that the expressed protein can be stabilised by the presence of Cd in the corresponding complexes. The absolute amounts of this isoform in the snail may be very low. In other pulmonate species, this protein is not detectable at all after chromatographic isolation (cf. H. pomatia, Dallinger et al. 2005; Palacios et al. 2011). It is therefore suggested that exclusively in C. aspersus, CaCd/CuMT may function as a trapping molecule for excess traces of Cd and Cu during short-term events of acute exposure. Overall, its contribution to the trace element balance in the escargot may be of only marginal significance.
Conclusions
Cantareus aspersus possesses three MT isogenes: CaCuMT, CaCdMT, and CaCd/CuMT. As in other pulmonate snails, they have probably evolved by gene duplication from a common ancestor (Palacios et al. 2011). Only one (CaCdMT) of those genes is significantly upregulated by Cd, the other two genes (CaCuMT and CaCd/CuMT) are constitutively expressed and do not respond at all or only slightly to long-term Cd or Cu induction. The protein products of these genes are devoted to differential tasks, with two of them showing metal specificity for Cu (CaCuMT) or Cd (CaCdMT) and one non metal-specific isoform (CaCd/CuMT) natively binding Cd and Cu simultaneously. The CaCdMT protein binds most of the Cd absorbed by the snail tissues. Data of the present work and results from earlier studies (Hispard et al. 2008; Palacios et al. 2011) suggest that the CaCdMT isoform may account for 80–90% of the total Cd balance in snails exposed to this metal. In uncontaminated snails, this isoform is virtually absent or present at very low concentrations as a Zn complex (Egg et al. 2009). An important role for Cu balance and metabolism is attributed to the CaCuMT isoform, irrespective of whether snails are exposed to contaminating Cu or not. This is due to the fact that the CaCuMT isoform is highly Cu-specific (see present study) binding a constant fraction of Cu absorbed by the snail tissues, mostly in rhogocytes (Dallinger et al. 2005). It is speculated that this MT-bound Cu may be available for the synthesis of the respiratory haemocyanin which represents the second significant Cu containing pool in most pulmonate snails. In addition, there are significant Cu pools present in granular cell fractions of rhogocytes, probably not in the form of a protein, and mainly in response to acute Cu exposure (Dallinger et al. 2005). Thus the share of CaCuMT in the total Cu metabolism of C. aspersus may be significant, although not sufficient to cover the Cu balance of the snail entirely. Its contribution to the Cu status of this species may range between 30 and 50%.
The contribution of the unspecific CaCd/CuMT isoform to the metal status of C. aspersus is obviously less important. This isoform may trap after Cd or Cu exposurea certain proportion of these metals. It is not present, however, under control conditions. Moreover, this isoform cannot normally be detected in other pulmonate species (Dallinger et al. 2005; Palacios et al. 2011). Because of these facts, it is suggested that its contribution to the metal status of C. aspersus may be low to negligible, this isoform possibly being more interesting from an evolutionary point of view. The CaCd/Cu sequence is more similar to that of CuMT isoforms than to CdMT snail isoforms. The corresponding gene is constitutively expressed, like most Cu-thionein genes, although Cd slightly enhances its transcription resulting in natively mixed Cd, Cu-complexes. Concordantly, recombinant analysis of its metal-binding behaviour reveals neither a genuine Cd- nor Cu-binding aptitude, even though some features, such as the production of sulfide-containing Cd-complexes when synthesised in cultures enriched with this metal ion, suggest a closer relationship of this isoform to Cu- than to Cd-thioneins (Bofill et al. 2009). In fact, a more detailed study (manuscript in preparation) of the structure/function relationship of this metal-binding peptide may elucidate the sequence determinants for metal specificity in MTs, i.e. which amino acids in what position favour the balance towards a Cd-thionein (divalent ion-thionein) or Cu-thionein.
Abbreviations
- AAS:
-
Atomic absorption spectrophotometry
- CaMT:
-
C. aspersus MT (global denomination)
- CaCdMT:
-
Cd-specific C. aspersus MT isoform
- CaCuMT:
-
Cu-specific C. aspersus MT isoform
- CaCd/CuMT:
-
Mixed metal C. aspersus MT isoform
- ESI-MS:
-
Electrospray ionization mass spectrometry
- ESI-TOF MS:
-
Time-of-flight electrospray ionization mass spectrometry
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Acknowledgments
This work was supported by the Spanish Ministerio de Ciencia y Tecnología grants BIO2009-12513-C02-01 to S. Atrian, BIO2009-12513-C02-02 to M. Capdevila and project No. P19782-B02 from the Austrian Science Foundation to R. Dallinger. Collaboration between the Spanish and Austrian research groups was financed by the “Acciones Integradas” grants HU2006-0027 (Spain) and ES 02/2007 (Austria). Authors from the University of Innsbruck are members of “Centre of Molecular Biosciences Innsbruck” (CMBI). Authors from the Universitat Autònoma de Barcelona (UAB) and Universitat de Barcelona (UB) are members of a “Grups de Recerca de la Generalitat de Catalunya” (2009SGR-1457). We thank the Serveis Cientificotècnics of UB (GC-FPD, ICP-AES, DNA sequencing) and the Servei d’Anàlisi Química (SAQ) of UAB (CD, UV–vis, ESI-MS) for allocating instrument time.
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Höckner, M., Stefanon, K., de Vaufleury, A. et al. Physiological relevance and contribution to metal balance of specific and non-specific Metallothionein isoforms in the garden snail, Cantareus aspersus . Biometals 24, 1079–1092 (2011). https://doi.org/10.1007/s10534-011-9466-x
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DOI: https://doi.org/10.1007/s10534-011-9466-x