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Article

Different Toxicity Mechanisms for Citrinin and Ochratoxin A Revealed by Transcriptomic Analysis in Yeast

1
Department of Biotechnology, Instituto de Biología Molecular y Celular de Plantas, Universidad Politécnica de Valencia, Ingeniero Fausto Elio s/n, 46022 Valencia, Spain
2
Department of Molecular and Cellular Pathology and Therapy, Instituto de Biomedicina de Valencia IBV-CSIC, Jaime Roig 11, 46010 Valencia, Spain
*
Authors to whom correspondence should be addressed.
Toxins 2016, 8(10), 273; https://doi.org/10.3390/toxins8100273
Submission received: 27 July 2016 / Revised: 13 September 2016 / Accepted: 17 September 2016 / Published: 22 September 2016
(This article belongs to the Collection Understanding Mycotoxin Occurrence in Food and Feed Chains)

Abstract

:
Citrinin (CIT) and ochratoxin A (OTA) are important mycotoxins, which frequently co-contaminate foodstuff. In order to assess the toxicologic threat posed by the two mycotoxins separately or in combination, their biological effects were studied here using genomic transcription profiling and specific live cell gene expression reporters in yeast cells. Both CIT and OTA cause highly transient transcriptional activation of different stress genes, which is greatly enhanced by the disruption of the multidrug exporter Pdr5. Therefore, we performed genome-wide transcription profiling experiments with the pdr5 mutant in response to acute CIT, OTA, or combined CIT/OTA exposure. We found that CIT and OTA activate divergent and largely nonoverlapping gene sets in yeast. CIT mainly caused the rapid induction of antioxidant and drug extrusion-related gene functions, while OTA mainly deregulated developmental genes related with yeast sporulation and sexual reproduction, having only a minor effect on the antioxidant response. The simultaneous exposure to CIT and OTA gave rise to a genomic response, which combined the specific features of the separated mycotoxin treatments. The application of stress-specific mutants and reporter gene fusions further confirmed that both mycotoxins have divergent biological effects in cells. Our results indicate that CIT exposure causes a strong oxidative stress, which triggers a massive transcriptional antioxidant and drug extrusion response, while OTA mainly deregulates developmental genes and only marginally induces the antioxidant defense.

Graphical Abstract

1. Introduction

Mycotoxins are small toxic molecules produced by a great variety of microorganism, which encompass several classes of secondary metabolites with no common chemical structure or mode of action [1]. These harmful natural products of molds contaminate food and feed worldwide with appalling economic consequences, since they affect most of the staple food crops such as maize, wheat and rice [2,3]. Beyond the economic losses, mycotoxins have a severe impact on human wellbeing [4]. Their toxicological properties and possible health effects have been extensively studied and related to some diseases, although it is certainly difficult to demonstrate the link between toxin exposure and the onset of symptoms in most cases. Mycotoxins are released by some fungi in nature for unclear reasons, and although it is widely accepted that the synthesis and secretion of toxins mediate pathogen virulence of microorganisms in plants, the molecular targets and strategies to achieve it remain to be determined in the case of mycotoxins [5]. Considerable efforts have been made to comprehend the molecular mechanisms of mycotoxins to cause cell damage and toxicity [6,7,8]. Although it is desirable to understand the molecular basis of mycotoxin action in whole animals, these approaches are often difficult because the dose-effect relation depends on many different parameters [7]. As an alternative, the fundamental modes of toxicity for individual mycotoxins can be efficiently revealed in cell cultures of lower eukaryotic cells such as yeast.
Ochratoxins are a small group of mycotoxins produced by Aspergillus and Penicillium species, with ochratoxin A (OTA) as the principal compound, found in a very wide range of raw and processed food [9]. OTA is nephrotoxic, carcinogenic, and a potent teratogen when tested in different mammalian models, and thereby is a potential risk to human health [10]. Several authors support that the mode of action of OTA implies the formation of covalent DNA adducts [11,12,13] and the increase of reactive oxygen species [14,15], hence these activities could explain the genotoxic and mutagenic activity of OTA. The co-occurrence of OTA with citrinin (CIT), another mycotoxin, has been often reported [16,17]. CIT is produced by filamentous fungi of the genera Penicillium, Aspergillus and Monascus, and contaminates the same staple foodstuffs as OTA [18]. Fungi such as Penicillium verrucosum are able to produce both OTA and CIT, however, different environmental conditions might favor the production of one mycotoxin over the other [19,20,21]. Much less is known about the toxicity mechanisms of CIT, however, it has been shown to be an efficient nephrotoxin as well [22]. Several groups have contributed to the identification of possible molecular mechanisms of CIT toxicity, finding, among other consequences, the increase of oxidative stress in connection with alterations of mitochondrial function, and induction of apoptosis [23,24,25,26,27,28,29,30,31]. It has been proposed that the co-occurrence of both toxins results in synergetic effects, however no clear conclusions have been reached [32,33].
Gene expression analysis has become a valuable tool to decipher molecular mechanisms in response to toxic agents, including mycotoxins [34], and the yeast model is particularly important in toxicogenomic studies [35]. Recent transcriptomic approaches with OTA have been performed using different cell lines and mammalian model systems [36,37,38,39]. A comparison of the genomic data does not yield a uniform pattern of deregulated genes, and it is striking that DNA damage response genes are not generally highlighted by these omics approaches [40]. It seems that the variability of the OTA-induced transcriptomic response might be a consequence of the range of experimental conditions as well as the cellular context [40]. In contrast to OTA, genomic profiling data for CIT treatment are scarce, however, the application of yeast microarray approaches has identified the antioxidant defense as one of the primordial manners of detoxification upon CIT exposure [41]. The transcriptional response to mycotoxins is likely to be transient and dose dependent, therefore any transcriptomic assay is further complicated by the selection of the optimal induction conditions. Actually, in vivo recording of transcriptional activity in Saccharomyces cerevisiae shows a transient dose–time dependent response to CIT treatment [28].
Given that OTA and CIT are co-occurring toxicological threats in the food chain and that both overlapping and divergent mechanisms of toxicity have been proposed for both mycotoxins, we aim here to compare the immediate transcriptomic response to OTA and CIT, applied either separately or simultaneously. We use an optimized yeast system, where the optimal time point and dose for each mycotoxin has been adjusted according to live cell gene expression reporters and where the signal intensity has been largely increased due to the deletion of the principal toxin exporter Pdr5. We identify largely exclusive patterns of gene deregulation for CIT and OTA, with oxidative stress defense genes specifically activated by CIT and cell differentiation and developmental genes specifically activated by OTA.

2. Results

2.1. Gene Expression Profiles of Stress Response Genes upon CIT and OTA Exposure

We have previously shown that live cell reporter fusions in yeast are valuable and quantitative tools to characterize the acute transcriptional adaptation to CIT [28]. Here, we extend these studies to compare the impact of CIT and OTA on the induction of different stress-inducible genes. We used fusions of the oxidative stress-inducible SOD2 (mitochondrial manganese superoxide dismutase) promoter and the general stress-inducible GRE2 (methylglyoxal reductase) promoter with destabilized luciferase as sensitive live cell reporters. Dose-dependent analyses revealed a transient gene expression profile for both reporter genes, upon treatment with CIT and OTA (Figure 1A). Both mycotoxins induced gene expression very rapidly within minutes, indicating that CIT and OTA are readily taken up by yeast cells. However, CIT caused a much broader transcriptional induction, which continuously increased with dose even beyond 400 ppm (1600 μM). OTA, in contrast, induced the stress-responsive reporters in a much more transient manner and to much lower absolute induction levels. Moreover, OTA-induced transcription of GRE2 or SOD2 was already maximal at concentrations around 200 ppm (497 μM). We next tested the effect of the loss of Pdr5 function, which is a plasma membrane multidrug transporter critically involved in CIT extrusion [28]. As shown in Figure 1B, the deletion of Pdr5 provokes an enhanced transcriptional response to both CIT and OTA treatment at different doses. We next wanted to study the level of synergy involved in the response to CIT and OTA using the same live cell gene expression reporters. Surprisingly, no evident synergistic effect on gene expression was revealed when both toxins were combined together, both in the wild type or the sensitized pdr5 mutant strain (Figure 1C). Taken together, these results indicated that CIT and OTA had differential and independent effects on the induction of stress reporters in yeast. Thus we aimed at studying the differential induction of gene expression upon CIT and OTA exposure at the genomic level.

2.2. Genomic Expression Profiles upon Separated and Combined Exposure to CIT and OTA

Our previous study of specific stress promoters suggested that CIT and OTA had a different impact on gene expression. Both mycotoxins, however, activate gene transcription in a very transient manner. We wanted to take advantage of genome-wide transcription analysis in yeast to gain insights into the differential induction of gene expression triggered by the two mycotoxins. The microarray experiments were performed in the sensitized pdr5 mutant strain and at optimized toxin concentrations and exposure times as revealed by our real time surveys upon acute CIT and OTA exposure. The transcriptomic response of yeast was determined by microarray hybridization upon separated CIT and OTA exposure (200 ppm) as well as upon the combined addition of CIT/OTA (100 ppm each). As a first approach, we identified and ranked the most upregulated genes for each toxin treatment. We applied a very stringent cutoff value and considered only the genes which were expressed more than 5-fold higher in the treated cells as compared to the untreated cells. The resulting gene lists are represented in Table 1 for CIT, in Table 2 for OTA, and in Table 3 for the combined CIT/OTA treatment.
Acute CIT exposure provoked the robust upregulation of 68 yeast genes. When classified for the most statistically relevant functional groups, we identified the response to oxidative stress as the dominant group (see Table 4). These data confirmed that CIT toxicity is fundamentally based on its capacity to generate reactive oxygen species (ROS) in cells. Specifically, genes involved in the metabolism of glutathione were preferentially expressed upon CIT exposure, indicating that the antioxidant function of glutathione was necessary to palliate the toxic effect of CIT. Additionally we identified “Drug transport” as a main CIT-inducible gene group, suggesting that the activated export of the toxin might be a major determinant for the adaptation of yeast cells to CIT.
For OTA exposure, we were able to identify 115 genes whose expression was at least 5-fold induced (Table 2). The analysis of the functional groups enriched in the dataset derived from OTA-treated cells revealed that the “response to oxidative stress” was retrieved with much less significance as compared to the CIT dataset. In turn, we identified yet other functional groups as most significantly upregulated by OTA, which belong to developmental processes of yeast cells and specifically to the differentiation processes of sporulation and reproduction (see Table 4). These data indicated that both mycotoxins induced different gene sets in yeast. Indeed, the comparison of the most significantly upregulated genes revealed that less than 5% (a total of only 8 genes) of the transcripts were induced commonly by either CIT or OTA as depicted in Figure 2. The subset of CIT- and OTA-responsive genes was enriched for the functional category “Oxidation–reduction process”. These results clearly showed that CIT and OTA induced largely separated gene sets in the initial adaptive phase, which suggested that both mycotoxins might have different biological effects in yeast cells. We next analyzed the transcriptomic response of yeast cells to the combined exposure of CIT and OTA. A total of 68 transcripts were significantly upregulated >5-fold under these conditions (see Table 3). The functional gene groups enriched by the combined mycotoxin treatment represented a combination of the gene functions induced in the previous experiments by the separated toxin treatment. As a result, all categories covering “oxidative stress response”, “drug transport”, “developmental processes”, and “sporulation” were significantly enriched upon the combined CIT/OTA exposure (see Table 4). Taken together, our transcriptomic survey of the response to CIT and OTA strongly supported the idea that both toxins cause distinct and separable biological responses. CIT caused a clear antioxidant response and the induction of multiple drug extrusion systems, while OTA seemed to retain a weak oxidation-related toxicity and to cause a marked deregulation of developmental genes. We wanted to further dissect these divergent toxicity effects of CIT and OTA in the yeast model.

2.3. Oxidative Stress is a Hallmark for CIT, but not OTA, Toxicity

According to our genomic expression experiments, CIT caused a specific antioxidant response in yeast cells, while antioxidant genes were only weakly induced by OTA. Additionally, CIT robustly induced the expression of a total of 7 different multidrug exporters (Flr1, Atr1, Snq2, Pdr15, Pdr10, Pdr16 and Yor1), while OTA moderately activated the expression of only the Snq2 drug exporter. We therefore wanted to quantify the importance of the antioxidant response and drug transport for the resistance to CIT or OTA. We employed specific yeast mutants with a defect in the oxidative stress adaptation (yap1, skn7) or multidrug export (snq2, yor1) and tested their resistance to CIT or OTA in comparison to wild type cells. As shown in Figure 3, the lack of the principal transcriptional activator of the oxidative stress defense Yap1 or of the multidrug transporter Snq2 rendered yeast cells hypersensitive to CIT, but not OTA. This sensitivity was observed after 8 h of toxin treatment. The deletion of a second transcription factor involved in the antioxidant response, Skn7, or an alternative multidrug exporter, Yor1, resulted in a weaker sensitivity phenotype exclusively in the case of CIT, which was observed after a prolonged toxin treatment (24 h). These data indicated that the antioxidant defense and the activated toxin export are key features for CIT detoxification, which are dispensable for the cellular defense against OTA.
We next wanted to test whether CIT and OTA caused different biological effects in the first instances of exposure. We therefore applied different live cell gene expression reporters in yeast cells to monitor transcriptional responses, which are triggered by distinct biological stimuli. Since we have previously shown that the Pdr5 drug transporter is important for the response to both CIT and OTA, we used a PDR5–luciferase expressing strain to monitor the induction of PDR5, which is activated by the accumulation of both toxins in the cell interior and not linked to a specific type of stress. Furthermore, we recorded the activation of two additional reporters, the general stress-inducible GRE2–luciferase, and the oxidative stress-inducible AP1–luciferase fusion [42]. We obtained the complete dose-response profiles of all three reporter strains upon increasing CIT and OTA exposures (Figure 4A). The relationship between the toxin dose and the transcriptional output (Amax) allowed us to visualize the relative sensibilities, with which each reporter was activated by the two mycotoxins (Figure 4B), and to observe important differences. Both CIT and OTA induced the PDR5–lucCP reporter with similar dose-response kinetics. However, the stress-specific GRE2 and AP1 reporters were activated by CIT in a much more sensitive manner as compared to OTA (Figure 4B). Remarkably, the oxidative stress specific AP1–luciferase reporter remained completely uninduced even at the highest OTA concentrations. These data, together with the previous phenotypic analysis of specific yeast mutants, clearly indicated that CIT and OTA have divergent biological effects in cells. Taking together all the results presented here, CIT exposure causes strong oxidative stress, which triggers a massive transcriptional antioxidant and drug extrusion response, while OTA mainly deregulates developmental genes and only marginally induces the antioxidant defense.

3. Discussion

Here we compare the toxicity targets of the mycotoxins ochratoxin A and citrinin using yeast as a model. Saccharomyces cerevisiae is a very suitable organism to investigate the adaptive response triggered by OTA and CIT, because both toxins cause rapid and profound changes in gene expression in yeast. Moreover, yeast transcriptional responses can be compared quantitatively in real time for different stress-specific reporters and additionally on a genomic scale. These approaches are thus suitable as a diagnostic tool to discern divergent and common biological effects of toxins. It is important to note that yeast cells seem to resist much higher CIT and OTA doses as compared to mammalian cells. The reasons for this might be a very efficient extrusion by multidrug transporters in this organism—which is shown here as being especially relevant for CIT detoxification—or the function of the yeast cell wall, which might serve as a primary barrier for mycotoxins. The adsorption by the yeast cell wall is actually an emerging biotechnological approach to control the concentration of different mycotoxins including OTA [43,44].
A common defense strategy of eukaryotic cells against many unrelated toxic compounds and xenobiotics is the activation of multidrug transporters at the plasma membrane [45,46]. In yeast cells, such as in other fungi and human cells, the intracellular levels of toxic molecules are directly sensed by specialized transcription factors, which in turn activate the expression of multidrug transporter genes in an attempt to physically extrude the toxic agents from the cell interior [47]. Here we take advantage of a specific drug efflux pump, Pdr5, which seems to be important for both CIT and OTA detoxification. Mutants for Pdr5 respond in a much more sensitive manner to both mycotoxins, as indicated by a more pronounced transcriptional activation of stress reporters by lower toxin concentrations. Although not tested directly, we assume that pdr5 mutant cells accumulate higher CIT and OTA concentrations. We took advantage of this sensitivity phenotype to carry out genomic profiling experiments. The use of a hypersensitive mutant strain and the selection of optimized toxin concentrations and time points for sample preparation favored the identification of many significantly deregulated gene functions in the immediate response to both compounds. We show that the expression of the PDR5 gene is activated by CIT and OTA with similar dose response profiles (Figure 3B). This result indicates that both mycotoxins are similarly taken up by yeast cells and that the differences in the gene expression profiles are not due to a differential intracellular accumulation of the two compounds.
Citrinin induces the expression of many different multidrug transporters, and the functional category “Drug membrane transport” is significantly enriched among the CIT target genes. Seven multidrug exporter genes are highly induced by CIT: FLR1, ATR1, SNQ2, PDR15, PDR10, PDR16, and YOR1. All of these transporters are localized, at least in part, at the plasma membrane. Thus the inducible active transport of CIT from the cytosol to the cell exterior is an important feature of detoxification of this mycotoxin in yeast cells. Accordingly, we detect an increased sensitivity to CIT by the loss of individual transporters such as Pdr5, Snq2 or Yor1. OTA, however, has a much weaker impact on the induction of the multidrug extrusion system, which coincides with the CIT response only in the moderate induction of the SNQ2 gene. Of note, the yeast pleiotropic drug response is activated by the mere presence of the compound in the cell interior and also by the cytotoxic stress triggered by the compound. Thus the higher impact of CIT on the ROS balance of the cell as compared to OTA could result in a much more profound transcriptional activation of the multidrug export system.
Here we show that the predominant mechanism of CIT toxicity is the induction of oxidative stress. Moreover, oxidative stress reporters are immediately upregulated upon CIT exposure and yeast mutants with a weakened antioxidant defense are hypersensitive to this mycotoxin, which altogether suggests that the induction of ROS inside cells is a primary mode of CIT action. Our result is in agreement with a previous transcriptomic assay in yeast upon prolonged CIT treatment [41] and with several studies showing CIT induced oxidative damage in diverse cellular models from yeast to humans [26,27,28,30]. As a consequence, external addition of antioxidants usually alleviates CIT toxicity [25,48,49]. How, at the molecular level, CIT increases intracellular ROS levels is currently unknown, however, several studies have implied an inhibition of mitochondrial respiration in CIT-activated oxidative stress [29,31,50]. On the other hand, we demonstrate here that OTA has a much less pronounced impact on the yeast antioxidant response at the genomic level, which is further corroborated by specific oxidative stress reporters. Thus, oxidative stress might not be the primary toxicity mechanism for this mycotoxin. This divergent impact of CIT and OTA on ROS production is in complete agreement with a recent study showing that CIT-, but not OTA-induced hepatotoxicity, is efficiently counteracted by antioxidant treatment [49]. However, the genomic response of yeast to OTA does include the upregulation of some antioxidant functions, which interestingly are different from the antioxidant genes induced by CIT. OTA induces, for example, the expression of both mitochondrial/peroxisomal and cytosolic catalases (Ctt1 and Cta1), while CIT preferentially stimulates enzymatic functions involved in glutathione metabolism (Ecm4, Glr1, Gsh1, Gtt2, and Grx2). Thus, apart from considerable differences in absolute ROS induction, it might be possible that CIT and OTA produce distinct types of reactive oxygen species. These differences are striking because CIT and OTA are structurally related mycotoxins. Both share a dihydroisocoumarin moiety as the central structure element, which is coupled to the amino acid phenylalanine in the case of OTA. However, a functional divergence has been suggested also with respect to the environmental conditions, which induce the biosynthesis of CIT or OTA in their natural producer Penicillium verrucosum. Here different stress conditions, such as oxidative or salt stress, have been shown to differentially favor the production of one mycotoxin over the other [19,20].
Despite a large scientific effort, the critical mechanism underlying OTA cytotoxicity still remains unknown. Oxidative stress has been widely implied in OTA action [15], but it certainly cannot explain the carcinogenic properties of this mycotoxin. Here we confirm that OTA is able to trigger an antioxidant response in yeast, however, ROS production is not the principle effect of OTA. This is in agreement with recent studies, which demonstrate in rats that renal carcinogenicity and cell cycle aberrations caused by OTA cannot be explained by oxidative damage [51,52]. Here we show that OTA treatment causes a general deregulation of developmental genes in yeast. This effect is OTA-specific and is not observed upon CIT exposure. The affected gene functions are related to the processes of meiosis and sporulation, which are normally tightly repressed in haploid yeast cells such as the strains used here for the transcriptomic experiments. Therefore, OTA seems to cause a genomic reprogramming of a developmental process, which is normally exclusively triggered in diploid yeast cells upon the appropriate environmental stimuli [53,54]. A tight epigenetic control, composed of specific DNA-binding factors which recruit histone deacetylases such as the Hst1 sirtuin to meiotic and sporulation genes, are known in yeast to assure repression of these developmental genes in haploid cells [55,56,57]. How OTA can interfere with the epigenetic control of silenced genes in yeast is currently only speculative, but opens an emerging research towards the biological function of this mycotoxin. This is of outstanding importance because the interference with gene silencing and the function of sirtuin histone deacetylases are hallmarks in the reprogramming of cancer cells [58,59] and thus could provide insights into the carcinogenic function of OTA. Taken together, our results demonstrate divergent biological effects of two related mycotoxins, which will be important for understanding their toxicity mechanisms at the molecular level.

4. Materials and Methods

4.1. Yeast Strains and Growth Conditions

Saccharomyces cerevisiae strains used in this study were: wild type BY4741 (MATa; his3Δ1; leu2Δ0; met15Δ0; ura3Δ0) and the mutant alleles yap1::KanMX4; skn7::KanMX4; yor1::KanMX4; pdr5::KanMX4; snq2::KanMX4. For luciferase assays the cells were transformed with the respective lucCP+ fusion plasmids and grown in synthetic dextrose (SD) medium which contained 0.67% yeast nitrogen base, 50 mM succinic acid pH 5.5, 2% dextrose, 100 mg/L methionine, 100 mg/L leucine, and 25 mg/L uracil. For CIT and OTA sensitivity assays on agar plates, the respective yeast strains were grown in SD liquid medium containing 2% dextrose to exponential growth phase and then incubated with 400 μM of CIT or OTA for the indicated time in small culture aliquots in multiwell plates at 28 °C. Citrinin and ochratoxin A were purchased from Enzo Life Sciences (Farmingdale, NY, USA), and stock solutions were prepared with DMSO as the solvent.

4.2. Plasmid Constructions

The destabilized luciferase reporter fusions with the natural GRE2 or SOD2 promoters are described elsewhere [60,61]. Briefly, the GRE2–lucCP+ fusion contains the upstream 940 nucleotides of the GRE2 gene fused with the destabilized luciferase lucCP+ gene in a centromeric HIS3-containing yeast expression plasmid. The SOD2–lucCP+ fusion contains the upstream 977 nucleotides of the SOD2 gene in the same vector backbone. The AP-1-specific destabilized luciferase reporter is described in [60]. Briefly, it contains a triple insertion of the AP-1 promoter element in the CYC1 core promoter fused to lucCP+ in centromeric HIS3-containing yeast expression plasmids. A PDR5–luciferase expressing reporter strain was created by integrative transformation of a PDR5–lucCP+–Kan MX DNA cassette into yeast wild type strain BY4741 to replace the endogenous PDR5 gene with the destabilized luciferase gene.

4.3. Live Cell Luciferase Assays

Yeast strains transformed with the respective luciferase reporter plasmids were grown at 28 °C overnight in SD medium to OD = 2 at 600 nm. The culture volume necessary for the entire luciferase assay was incubated on a roller at 28 °C for 90 min with 0.5 mM luciferin (Synchem, Felsberg, Germany) from a 10 mM stock solution in Dimethylsulfoxide. The culture was then distributed in 120 μL aliquots in white 96-well plates (Nunc, Penfield, NY, USA) and growing concentrations of CIT or OTA were added from a stock solution in DMSO. In Figure 1, 200 μM (= 50 ppm), 800 μM (= 200 ppm), and 1600 μM (= 400 ppm) of CIT and 124 μM (= 50 ppm), 497 μM (= 200 ppm), and 994 μM (= 400 ppm) of OTA were applied. Additionally, a constant dose of 200 μM (= 50 ppm) of CIT was combined with growing OTA concentrations (124 μM (= 50 ppm), 497 μM (= 200 ppm), and 994 μM (= 400 ppm)). In Figure 3, 20 μM, 40 μM, 100 μM, 200 μM, 400 μM, and 800 μM of CIT or OTA were used. The mock-treated samples contained the same concentration of solvent without the mycotoxin. The light emission from the culture aliquots was continuously recorded in a GloMax Multidetection System (Promega, Madison, WI, USA) in the luminometer mode. Data were normalized for the absolute number of cells used in the assay and processed in Microsoft Excel (2010). For each condition, three independent culture aliquots were analyzed. The maximal luciferase activity depicted in Figure 1C and Figure 4B was calculated by correcting the maximal light emission for each treatment with the value obtained for the mock-treated culture.

4.4. Yeast Sensitivity Assays

For plate assays, the yeast strains under study were grown in SD liquid medium to exponential growth phase. 1:1, 1:10 and 1:100 dilutions of culture aliquots were then distributed in multiwell plates and exposed for the indicated time to CIT or OTA added from stock solutions in DMSO. Equal amounts of cells were then plated on fresh yeast extract peptone dextrose (YPD) agar plates, which were incubated at 28 °C for 2 days.

4.5. Microarray Experiments and Analysis

For the comparison of the transcriptome upon various mycotoxin treatments, the pdr5 mutant strain was used. Cells were grown in SD medium until exponential phase and then subjected to four different toxin treatments: control (mock treated with solvent), CIT (200 ppm for 60 min), OTA (200 ppm for 30 min), and a combination of both mycotoxins CIT/OTA (100 ppm each for 30 min). Total RNA was prepared from four independent culture aliquots for each condition using the acid phenol extraction method. Total RNA was further purified with the RNeasy Mini kit (Qiagen, Valencia, CA, USA). The samples were labeled using the one-color method with Cy3 fluorophore, hybridized to Agilent Yeast Gene Expression 8 × 15 K microarrays, and scanned with Agilent DNA Microarray Scanner (G2505B, Agilent Technologies, Santa Clara, CA, USA). Raw data were obtained using the Feature Extraction software 9.5.1 (Agilent Technologies, Santa Clara, CA, USA, 2007). These procedures were performed by the Genomic Service of the Instituto de Biología Molecular y Celular de Plantas (IBMCP, Valencia, Spain). Data analysis was performed using GeneSpring 12.6 (Agilent Technologies, Santa Clara, CA, USA). Data were normalized using the quantile method and then statistically analyzed with the Student t-Test. Significant differences in gene expression were selected using a p-value < 0.05. To avoid the detection of false positives, a multiple testing correction (Bonferroni FWER) was applied to obtain corrected p-values. The complete dataset from all transcriptomic experiments of this publication has been assigned accession number GSE84187 in the Gene Expression Omnibus (GEO) Database. Significantly enriched functional gene groups were identified with the YeastMine Gene Ontology (GO) search option of the Saccharomyces cerevisiae Genome Database (SGD).

Acknowledgments

We thank Lorena Latorre and Javier Forment for their help with the microarray experiments and data analysis. This work was funded only in the initial phase by a grant from Ministerio de Economía y Competitividad (BFU2011-23326). We thank the Fond for Open Access Publication from Consejo Superior de Investigaciones Científicas (CSIC) for supporting publication costs of this article.

Author Contributions

M.P. and A.P.-A. conceived and designed the experiments; E.V.-P. performed the experiments; E.V.-P., M.P. and A.P.-A. analyzed the data; M.P. and A.P.-A. wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

References

  1. Bennett, J.W.; Klich, M. Mycotoxins. Clin. Microbiol. Rev. 2003, 16, 497–516. [Google Scholar] [CrossRef] [PubMed]
  2. Marroquin-Cardona, A.G.; Johnson, N.M.; Phillips, T.D.; Hayes, A.W. Mycotoxins in a changing global environment—A review. Food Chem. Toxicol. 2014, 69, 220–230. [Google Scholar] [CrossRef] [PubMed]
  3. Moretti, A.; Susca, A.; Mule, G.; Logrieco, A.F.; Proctor, R.H. Molecular biodiversity of mycotoxigenic fungi that threaten food safety. Int. J. Food Microbiol. 2013, 167, 57–66. [Google Scholar] [CrossRef] [PubMed]
  4. Wu, F.; Groopman, J.D.; Pestka, J.J. Public health impacts of foodborne mycotoxins. Annu. Rev. Food Sci. Technol. 2014, 5, 351–372. [Google Scholar] [CrossRef] [PubMed]
  5. Mobius, N.; Hertweck, C. Fungal phytotoxins as mediators of virulence. Curr. Opin. Plant. Biol. 2009, 12, 390–398. [Google Scholar] [CrossRef] [PubMed]
  6. Doi, K.; Uetsuka, K. Mechanisms of Mycotoxin-induced Dermal Toxicity and Tumorigenesis through Oxidative Stress-related Pathways. J. Toxicol. Pathol. 2014, 27, 1–10. [Google Scholar] [CrossRef] [PubMed]
  7. Escriva, L.; Font, G.; Manyes, L. In vivo toxicity studies of fusarium mycotoxins in the last decade: A review. Food. Chem. Toxicol. 2015, 78, 185–206. [Google Scholar] [CrossRef] [PubMed]
  8. Vettorazzi, A.; Gonzalez-Penas, E.; de Cerain, A.L. Ochratoxin A kinetics: A review of analytical methods and studies in rat model. Food Chem. Toxicol. 2014, 72, 273–288. [Google Scholar] [CrossRef] [PubMed]
  9. Wang, Y.; Wang, L.; Liu, F.; Wang, Q.; Selvaraj, J.N.; Xing, F.; Zhao, Y.; Liu, Y. Ochratoxin A Producing Fungi, Biosynthetic Pathway and Regulatory Mechanisms. Toxins 2016, 8. [Google Scholar] [CrossRef] [PubMed]
  10. Koszegi, T.; Poor, M. Ochratoxin A: Molecular Interactions, Mechanisms of Toxicity and Prevention at the Molecular Level. Toxins 2016, 8. [Google Scholar] [CrossRef] [PubMed]
  11. Faucet, V.; Pfohl-Leszkowicz, A.; Dai, J.; Castegnaro, M.; Manderville, R.A. Evidence for covalent DNA adduction by Ochratoxin A following chronic exposure to rat and subacute exposure to pig. Chem. Res. Toxicol. 2004, 17, 1289–1296. [Google Scholar] [CrossRef] [PubMed]
  12. Mantle, P.G.; Faucet-Marquis, V.; Manderville, R.A.; Squillaci, B.; Pfohl-Leszkowicz, A. Structures of covalent adducts between DNA and Ochratoxin A: A new factor in debate about genotoxicity and human risk assessment. Chem. Res. Toxicol. 2010, 23, 89–98. [Google Scholar] [CrossRef] [PubMed]
  13. Pfohl-Leszkowicz, A.; Manderville, R.A. An update on direct genotoxicity as a molecular mechanism of ochratoxin a carcinogenicity. Chem. Res. Toxicol. 2012, 25, 252–262. [Google Scholar] [CrossRef] [PubMed]
  14. Rahimtula, A.D.; Bereziat, J.C.; Bussacchini-Griot, V.; Bartsch, H. Lipid peroxidation as a possible cause of ochratoxin A toxicity. Biochem. Pharmacol. 1988, 37, 4469–4477. [Google Scholar] [CrossRef]
  15. Sorrenti, V.; di Giacomo, C.; Acquaviva, R.; Barbagallo, I.; Bognanno, M.; Galvano, F. Toxicity of ochratoxin a and its modulation by antioxidants: A review. Toxins 2013, 5, 1742–1766. [Google Scholar] [CrossRef] [PubMed]
  16. Bragulat, M.R.; Martinez, E.; Castella, G.; Cabanes, F.J. Ochratoxin A and citrinin producing species of the genus Penicillium from feedstuffs. Int. J. Food. Microbiol. 2008, 126, 43–48. [Google Scholar] [CrossRef] [PubMed]
  17. Vrabcheva, T.; Usleber, E.; Dietrich, R.; Martlbauer, E. Co-occurrence of ochratoxin A and citrinin in cereals from Bulgarian villages with a history of Balkan endemic nephropathy. J. Agric. Food. Chem. 2000, 48, 2483–2488. [Google Scholar] [CrossRef] [PubMed]
  18. Ostry, V.; Malir, F.; Ruprich, J. Producers and important dietary sources of ochratoxin A and citrinin. Toxins 2013, 5, 1574–1586. [Google Scholar] [CrossRef] [PubMed]
  19. Schmidt-Heydt, M.; Graf, E.; Stoll, D.; Geisen, R. The biosynthesis of ochratoxin A by Penicillium as one mechanism for adaptation to NaCl rich foods. Food Microbiol. 2012, 29, 233–241. [Google Scholar] [CrossRef] [PubMed]
  20. Schmidt-Heydt, M.; Stoll, D.; Schutz, P.; Geisen, R. Oxidative stress induces the biosynthesis of citrinin by Penicillium verrucosum at the expense of ochratoxin. Int. J. Food Microbiol. 2015, 192, 1–6. [Google Scholar] [CrossRef] [PubMed]
  21. Stoll, D.; Schmidt-Heydt, M.; Geisen, R. Differences in the regulation of ochratoxin A by the HOG pathway in Penicillium and Aspergillus in response to high osmolar environments. Toxins 2013, 5, 1282–1298. [Google Scholar] [CrossRef] [PubMed]
  22. Flajs, D.; Peraica, M. Toxicological properties of citrinin. Arh. Hig. Rada Toksikol. 2009, 60, 457–464. [Google Scholar] [CrossRef] [PubMed]
  23. Bouslimi, A.; Ouannes, Z.; Golli, E.E.; Bouaziz, C.; Hassen, W.; Bacha, H. Cytotoxicity and oxidative damage in kidney cells exposed to the mycotoxins ochratoxin a and citrinin: Individual and combined effects. Toxicol. Mech. Methods 2008, 18, 341–349. [Google Scholar] [CrossRef] [PubMed]
  24. Chan, W.H. Citrinin induces apoptosis via a mitochondria-dependent pathway and inhibition of survival signals in embryonic stem cells, and causes developmental injury in blastocysts. Biochem. J. 2007, 404, 317–326. [Google Scholar] [CrossRef] [PubMed]
  25. Kumar, M.; Dwivedi, P.; Sharma, A.K.; Sankar, M.; Patil, R.D.; Singh, N.D. Apoptosis and lipid peroxidation in ochratoxin A- and citrinin-induced nephrotoxicity in rabbits. Toxicol. Ind. Health 2014, 30, 90–98. [Google Scholar] [CrossRef] [PubMed]
  26. Kumar, R.; Dwivedi, P.D.; Dhawan, A.; Das, M.; Ansari, K.M. Citrinin-generated reactive oxygen species cause cell cycle arrest leading to apoptosis via the intrinsic mitochondrial pathway in mouse skin. Toxicol. Sci. 2011, 122, 557–566. [Google Scholar] [CrossRef] [PubMed]
  27. Mate, G.; Gazdag, Z.; Mike, N.; Papp, G.; Pocsi, I.; Pesti, M. Regulation of oxidative stress-induced cytotoxic processes of citrinin in the fission yeast Schizosaccharomyces pombe. Toxicon 2014, 90, 155–166. [Google Scholar] [CrossRef] [PubMed]
  28. Pascual-Ahuir, A.; Vanacloig-Pedros, E.; Proft, M. Toxicity mechanisms of the food contaminant citrinin: Application of a quantitative yeast model. Nutrients 2014, 6, 2077–2087. [Google Scholar] [CrossRef] [PubMed]
  29. Ribeiro, S.M.; Chagas, G.M.; Campello, A.P.; Kluppel, M.L. Mechanism of citrinin-induced dysfunction of mitochondria. V. Effect on the homeostasis of the reactive oxygen species. Cell. Biochem. Funct. 1997, 15, 203–209. [Google Scholar] [CrossRef]
  30. Singh, N.D.; Sharma, A.K.; Dwivedi, P.; Leishangthem, G.D.; Rahman, S.; Reddy, J.; Kumar, M. Effect of feeding graded doses of citrinin on apoptosis and oxidative stress in male Wistar rats through the F1 generation. Toxicol. Ind. Health 2016, 32, 385–397. [Google Scholar] [CrossRef] [PubMed]
  31. Yu, F.Y.; Liao, Y.C.; Chang, C.H.; Liu, B.H. Citrinin induces apoptosis in HL-60 cells via activation of the mitochondrial pathway. Toxicol. Lett. 2006, 161, 143–151. [Google Scholar] [CrossRef] [PubMed]
  32. Follmann, W.; Behm, C.; Degen, G.H. Toxicity of the mycotoxin citrinin and its metabolite dihydrocitrinone and of mixtures of citrinin and ochratoxin A in vitro. Arch. Toxicol. 2014, 88, 1097–1107. [Google Scholar] [CrossRef] [PubMed]
  33. Klaric, M.S.; Rasic, D.; Peraica, M. Deleterious effects of mycotoxin combinations involving ochratoxin A. Toxins 2013, 5, 1965–1987. [Google Scholar] [CrossRef] [PubMed]
  34. Afshari, C.A.; Hamadeh, H.K.; Bushel, P.R. The evolution of bioinformatics in toxicology: Advancing toxicogenomics. Toxicol. Sci. 2011, 120 (Suppl. 1), S225–S237. [Google Scholar] [CrossRef] [PubMed]
  35. Yasokawa, D.; Iwahashi, H. Toxicogenomics using yeast DNA microarrays. J. Biosci. Bioeng. 2010, 110, 511–522. [Google Scholar] [CrossRef] [PubMed]
  36. Arbillaga, L.; Azqueta, A.; van Delft, J.H.; Lopez de Cerain, A. In vitro gene expression data supporting a DNA non-reactive genotoxic mechanism for ochratoxin A. Toxicol. Appl. Pharmacol. 2007, 220, 216–224. [Google Scholar] [CrossRef] [PubMed]
  37. Hibi, D.; Kijima, A.; Kuroda, K.; Suzuki, Y.; Ishii, Y.; Jin, M.; Nakajima, M.; Sugita-Konishi, Y.; Yanai, T.; Nohmi, T.; et al. Molecular mechanisms underlying ochratoxin A-induced genotoxicity: Global gene expression analysis suggests induction of DNA double-strand breaks and cell cycle progression. J. Toxicol. Sci. 2013, 38, 57–69. [Google Scholar] [CrossRef] [PubMed]
  38. Hundhausen, C.; Boesch-Saadatmandi, C.; Matzner, N.; Lang, F.; Blank, R.; Wolffram, S.; Blaschek, W.; Rimbach, G. Ochratoxin a lowers mRNA levels of genes encoding for key proteins of liver cell metabolism. Cancer Genom. Proteom. 2008, 5, 319–332. [Google Scholar]
  39. Marin-Kuan, M.; Nestler, S.; Verguet, C.; Bezencon, C.; Piguet, D.; Mansourian, R.; Holzwarth, J.; Grigorov, M.; Delatour, T.; Mantle, P.; et al. A toxicogenomics approach to identify new plausible epigenetic mechanisms of ochratoxin a carcinogenicity in rat. Toxicol. Sci. 2006, 89, 120–134. [Google Scholar] [CrossRef] [PubMed]
  40. Vettorazzi, A.; van Delft, J.; Lopez de Cerain, A. A review on ochratoxin A transcriptomic studies. Food Chem. Toxicol. 2013, 59, 766–783. [Google Scholar] [CrossRef] [PubMed]
  41. Iwahashi, H.; Kitagawa, E.; Suzuki, Y.; Ueda, Y.; Ishizawa, Y.H.; Nobumasa, H.; Kuboki, Y.; Hosoda, H.; Iwahashi, Y. Evaluation of toxicity of the mycotoxin citrinin using yeast ORF DNA microarray and Oligo DNA microarray. BMC Genomics 2007, 8, 95. [Google Scholar] [CrossRef] [PubMed]
  42. Toone, W.M.; Morgan, B.A.; Jones, N. Redox control of AP-1-like factors in yeast and beyond. Oncogene 2001, 20, 2336–2346. [Google Scholar] [CrossRef] [PubMed]
  43. Luo, Y.; Wang, J.; Liu, B.; Wang, Z.; Yuan, Y.; Yue, T. Effect of yeast cell morphology, cell wall physical structure and chemical composition on patulin adsorption. PLoS ONE 2015, 10, e0136045. [Google Scholar] [CrossRef] [PubMed]
  44. Piotrowska, M.; Masek, A. Saccharomyces cerevisiae cell wall components as tools for ochratoxin A decontamination. Toxins 2015, 7, 1151–1162. [Google Scholar] [CrossRef] [PubMed]
  45. Jungwirth, H.; Kuchler, K. Yeast ABC transporters—A tale of sex, stress, drugs and aging. FEBS Lett. 2006, 580, 1131–1138. [Google Scholar] [CrossRef] [PubMed]
  46. Prasad, R.; Goffeau, A. Yeast ATP-binding cassette transporters conferring multidrug resistance. Annu. Rev. Microbiol. 2012, 66, 39–63. [Google Scholar] [CrossRef] [PubMed]
  47. Thakur, J.K.; Arthanari, H.; Yang, F.; Pan, S.J.; Fan, X.; Breger, J.; Frueh, D.P.; Gulshan, K.; Li, D.K.; Mylonakis, E.; et al. A nuclear receptor-like pathway regulating multidrug resistance in fungi. Nature 2008, 452, 604–609. [Google Scholar] [CrossRef] [PubMed]
  48. Chen, C.C.; Chan, W.H. Inhibition of citrinin-induced apoptotic biochemical signaling in human hepatoma G2 cells by resveratrol. Int. J. Mol. Sci. 2009, 10, 3338–3357. [Google Scholar] [CrossRef] [PubMed]
  49. Gayathri, L.; Dhivya, R.; Dhanasekaran, D.; Periasamy, V.S.; Alshatwi, A.A.; Akbarsha, M.A. Hepatotoxic effect of ochratoxin A and citrinin, alone and in combination, and protective effect of vitamin E: In vitro study in HepG2 cell. Food Chem. Toxicol. 2015, 83, 151–163. [Google Scholar] [CrossRef] [PubMed]
  50. Aleo, M.D.; Wyatt, R.D.; Schnellmann, R.G. The role of altered mitochondrial function in citrinin-induced toxicity to rat renal proximal tubule suspensions. Toxicol. Appl. Pharmacol. 1991, 109, 455–463. [Google Scholar] [CrossRef]
  51. Qi, X.; Yu, T.; Zhu, L.; Gao, J.; He, X.; Huang, K.; Luo, Y.; Xu, W. Ochratoxin A induces rat renal carcinogenicity with limited induction of oxidative stress responses. Toxicol. Appl. Pharmacol. 2014, 280, 543–549. [Google Scholar] [CrossRef] [PubMed]
  52. Taniai, E.; Yafune, A.; Nakajima, M.; Hayashi, S.M.; Nakane, F.; Itahashi, M.; Shibutani, M. Ochratoxin A induces karyomegaly and cell cycle aberrations in renal tubular cells without relation to induction of oxidative stress responses in rats. Toxicol. Lett. 2014, 224, 64–72. [Google Scholar] [CrossRef] [PubMed]
  53. Govin, J.; Berger, S.L. Genome reprogramming during sporulation. Int. J. Dev. Biol. 2009, 53, 425–432. [Google Scholar] [CrossRef] [PubMed]
  54. Winter, E. The Sum1/Ndt80 transcriptional switch and commitment to meiosis in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 2012, 76, 1–15. [Google Scholar] [CrossRef] [PubMed]
  55. Grunstein, M.; Gasser, S.M. Epigenetics in Saccharomyces cerevisiae. Cold Spring Harb. Perspect. Biol. 2013, 5. [Google Scholar] [CrossRef] [PubMed]
  56. Pijnappel, W.W.; Schaft, D.; Roguev, A.; Shevchenko, A.; Tekotte, H.; Wilm, M.; Rigaut, G.; Seraphin, B.; Aasland, R.; Stewart, A.F. The S. cerevisiae SET3 complex includes two histone deacetylases, Hos2 and Hst1, and is a meiotic-specific repressor of the sporulation gene program. Genes Dev. 2001, 15, 2991–3004. [Google Scholar] [CrossRef] [PubMed]
  57. Xie, J.; Pierce, M.; Gailus-Durner, V.; Wagner, M.; Winter, E.; Vershon, A.K. Sum1 and Hst1 repress middle sporulation-specific gene expression during mitosis in Saccharomyces cerevisiae. EMBO J. 1999, 18, 6448–6454. [Google Scholar] [CrossRef] [PubMed]
  58. Chalkiadaki, A.; Guarente, L. The multifaceted functions of sirtuins in cancer. Nat. Rev. Cancer 2015, 15, 608–624. [Google Scholar] [CrossRef] [PubMed]
  59. Roth, M.; Chen, W.Y. Sorting out functions of sirtuins in cancer. Oncogene 2014, 33, 1609–1620. [Google Scholar] [CrossRef] [PubMed]
  60. Dolz-Edo, L.; Rienzo, A.; Poveda-Huertes, D.; Pascual-Ahuir, A.; Proft, M. Deciphering dynamic dose responses of natural promoters and single cis elements upon osmotic and oxidative stress in yeast. Mol. Cell. Biol. 2013, 33, 2228–2240. [Google Scholar] [CrossRef] [PubMed]
  61. Rienzo, A.; Pascual-Ahuir, A.; Proft, M. The use of a real-time luciferase assay to quantify gene expression dynamics in the living yeast cell. Yeast 2012, 29, 219–231. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Ochratoxin A (OTA) and citrinin (CIT) activate stress gene expression independently and with different dose response profiles. (A) OTA and CIT induction of the stress-activated genes GRE2 (methylglyoxal reductase) and SOD2 (superoxide dismutase). Live cell reporter fusions with destabilized luciferase were used in yeast wild type cells and the induction of both genes was measured in real time upon the indicated mycotoxin doses. (B) The deletion of the Pdr5 multidrug exporter increases the transcriptional response to both OTA and CIT. The expression profiles for the GRE2 and SOD2 genes are compared for wild type and the pdr5 deletion mutant upon the indicated mycotoxin doses. (C) OTA and CIT do not activate stress gene expression in a synergistic manner. The dose response profiles of (A) and (B) are represented here as the maximal activity (Amax) for each mycotoxin dose. Additionally (purple columns at the right of each plot), a constant concentration of CIT (50 ppm = 200 μM) was combined with growing concentrations of OTA (50 ppm = 124 μM; 200 ppm = 497 μM; 400 ppm = 994 μM) as indicated. All gene expression experiments were performed on three independent culture aliquots; the Standard Deviation was <15%; error bars are not included in the graphs in order to make the figure clearly visible.
Figure 1. Ochratoxin A (OTA) and citrinin (CIT) activate stress gene expression independently and with different dose response profiles. (A) OTA and CIT induction of the stress-activated genes GRE2 (methylglyoxal reductase) and SOD2 (superoxide dismutase). Live cell reporter fusions with destabilized luciferase were used in yeast wild type cells and the induction of both genes was measured in real time upon the indicated mycotoxin doses. (B) The deletion of the Pdr5 multidrug exporter increases the transcriptional response to both OTA and CIT. The expression profiles for the GRE2 and SOD2 genes are compared for wild type and the pdr5 deletion mutant upon the indicated mycotoxin doses. (C) OTA and CIT do not activate stress gene expression in a synergistic manner. The dose response profiles of (A) and (B) are represented here as the maximal activity (Amax) for each mycotoxin dose. Additionally (purple columns at the right of each plot), a constant concentration of CIT (50 ppm = 200 μM) was combined with growing concentrations of OTA (50 ppm = 124 μM; 200 ppm = 497 μM; 400 ppm = 994 μM) as indicated. All gene expression experiments were performed on three independent culture aliquots; the Standard Deviation was <15%; error bars are not included in the graphs in order to make the figure clearly visible.
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Figure 2. Ochratoxin A and citrinin activate largely nonoverlapping gene sets in the yeast genome. Venn diagram comparing the >5-fold induced transcripts of the yeast genome upon OTA and CIT exposure. The exclusively upregulated genes by one mycotoxin (CIT or OTA) and the commonly upregulated genes are depicted in the table. The main functional groups associated with each gene cluster are given.
Figure 2. Ochratoxin A and citrinin activate largely nonoverlapping gene sets in the yeast genome. Venn diagram comparing the >5-fold induced transcripts of the yeast genome upon OTA and CIT exposure. The exclusively upregulated genes by one mycotoxin (CIT or OTA) and the commonly upregulated genes are depicted in the table. The main functional groups associated with each gene cluster are given.
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Figure 3. Citrinin, but not ochratoxin A, toxicity is exacerbated in mutants with a defective antioxidant response or multidrug export. The indicated yeast strains were treated or not with 400 μM CIT (upper panel) or 400 μM OTA (lower panel) for the indicated time. Serial dilutions 1:1, 1:10, and 1:100 of the yeast cultures were then assayed for survival on yeast extract peptone dextrose (YPD) agar plates without mycotoxins.
Figure 3. Citrinin, but not ochratoxin A, toxicity is exacerbated in mutants with a defective antioxidant response or multidrug export. The indicated yeast strains were treated or not with 400 μM CIT (upper panel) or 400 μM OTA (lower panel) for the indicated time. Serial dilutions 1:1, 1:10, and 1:100 of the yeast cultures were then assayed for survival on yeast extract peptone dextrose (YPD) agar plates without mycotoxins.
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Figure 4. CIT, as opposed to OTA, induces a sensitive oxidative and general stress response in yeast cells. (A) OTA and CIT induction of the PDR5–, GRE2– and AP1–luciferase reporters. Live cell reporter fusions with destabilized luciferase were used in yeast wild type cells and the induction of both genes was measured in real time upon the indicated mycotoxin doses. The data are derived from three independent culture aliquots and had an error of <15%. (B) Dose-response profiles of the different luciferase reporters. The maximal steady-state activity (Amax) was calculated for each reporter strain and toxin dose and plotted against the mycotoxin concentration. Amax for the highest toxin exposure was arbitrarily set to 100.
Figure 4. CIT, as opposed to OTA, induces a sensitive oxidative and general stress response in yeast cells. (A) OTA and CIT induction of the PDR5–, GRE2– and AP1–luciferase reporters. Live cell reporter fusions with destabilized luciferase were used in yeast wild type cells and the induction of both genes was measured in real time upon the indicated mycotoxin doses. The data are derived from three independent culture aliquots and had an error of <15%. (B) Dose-response profiles of the different luciferase reporters. The maximal steady-state activity (Amax) was calculated for each reporter strain and toxin dose and plotted against the mycotoxin concentration. Amax for the highest toxin exposure was arbitrarily set to 100.
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Table 1. Genes > 5-fold upregulated upon CIT (citrinin) exposure.
Table 1. Genes > 5-fold upregulated upon CIT (citrinin) exposure.
GeneStandard NameFC *p-ValueDescription
YPL171COYE3473.13.00 × 10−8Conserved NADPH oxidoreductase containing flavin mononucleotide (FMN)
YFL056CAAD6252.49.60 × 10−7Putative aryl-alcohol dehydrogenase
YDL243CAAD4252.11.77 × 10−9Putative aryl-alcohol dehydrogenase
YCL026C-AFRM2177.21.77 × 10−5Type II nitroreductase
YLL060CGTT2142.44.50 × 10−5Glutathione S-transferase
YBR008CFLR1120.61.83 × 10−7Plasma membrane multidrug transporter of the major facilitator superfamily
YCL026C-BHBN161.71.81 × 10−6Protein of unknown function
YGR213CRTA157.81.77 × 10−8Protein involved in 7-aminocholesterol resistance
YML116WATR154.81.45 × 10−7Multidrug efflux pump of the major facilitator superfamily
YKR076WECM451.66.10 × 10−6Omega class glutathione transferase
YML131W-41.29.44 × 10−3Protein of unknown function
YHR139CSPS10035.24.78 × 10−7Protein required for spore wall maturation
YFL057CAAD1633.52.12 × 10−2Putative aryl-alcohol dehydrogenase
YDR011WSNQ231.16.78 × 10−7Plasma membrane ATP-binding cassette (ABC) transporter
YOL151WGRE225.82.28 × 10−63-methylbutanal reductase and NADPH-dependent methylglyoxal reductase
YKL086WSRX125.65.22 × 10−7Sulfiredoxin
YDR406WPDR1518.11.12 × 10−6Plasma membrane ATP binding cassette (ABC) transporter
YLR108C-16.65.77 × 10−8Protein of unknown function
YDL020CRPN415.89.41 × 10−8Transcription factor that stimulates expression of proteasome genes
YNL117WMLS115.13.95 × 10−6Malate synthase
YOR328WPDR1014.52.41 × 10−8ATP-binding cassette (ABC) transporter
YHR199CAIM4613.31.58 × 10−7Putative protein of unknown function
YHR029CYHI912.93.86 × 10−7Protein of unknown function
YGR256WGND210.95.58 × 10−76-phosphogluconate dehydrogenase
YBR244WGPX210.53.56 × 10−6Phospholipid hydroperoxide glutathione peroxidase
YFL030WAGX110.34.28 × 10−8Alanine:glyoxylate aminotransferase (AGT)
YDR453CTSA29.62.01 × 10−7Stress inducible cytoplasmic thioredoxin peroxidase
YER143WDDI19.58.66 × 10−5DNA damage-inducible v-SNARE binding protein
YNR074CAIF19.14.46 × 10−7Mitochondrial cell death effector
YER042WMXR19.02.11 × 10−6Methionine-S-sulfoxide reductase
YJL101CGSH18.91.30 × 10−7Gamma glutamylcysteine synthetase
YHR138C-8.81.42 × 10−3Protein of unknown function
YHL036WMUP38.61.13 × 10−5Low affinity methionine permease
YNL129WNRK18.51.61 × 10−5Nicotinamide riboside kinase
YPR200CARR28.11.57 × 10−4Arsenate reductase
YER103WSSA47.82.65 × 10−5Heat shock protein
YJL045W-7.73.32 × 10−7Minor succinate dehydrogenase isozyme
YPL027WSMA17.79.86 × 10−7Protein of unknown function involved in prospore membrane assembly
YGR010WNMA27.51.02 × 10−7Nicotinic acid mononucleotide adenylyltransferase
YMR169CALD37.46.10 × 10−4Cytoplasmic aldehyde dehydrogenase
YDR132C-7.31.74 × 10−6Protein of unknown function
YOR162CYRR17.21.24 × 10−7Zn2-Cys6 zinc-finger transcription factor
YMR038CCCS16.96.96 × 10−5Copper chaperone for superoxide dismutase Sod1p
YJL219WHXT96.91.67 × 10−7Putative hexose transporter
YER142CMAG16.85.46 × 10−73-methyl-adenine DNA glycosylase
YBR046CZTA16.71.13 × 10−5NADPH-dependent quinone reductase
YNL231CPDR166.67.41 × 10−3Phosphatidylinositol transfer protein (PITP)
YPL091WGLR16.51.49 × 10−5Cytosolic and mitochondrial glutathione oxidoreductase
YGR281WYOR16.42.16 × 10−3Plasma membrane ATP-binding cassette (ABC) transporter
YGR197CSNG16.33.47 × 10−7Protein involved in resistance to nitrosoguanidine and 6-azauracil
YNL155WCUZ16.15.38 × 10−3Protein with a role in the ubiquitin-proteasome pathway
YAL054CACS16.13.74 × 10−7Acetyl-coA synthetase isoform
YOL119CMCH46.11.27 × 10−5Protein with similarity to mammalian monocarboxylate permeases
YDL168WSFA16.01.21 × 10−5Bifunctional alcohol dehydrogenase and formaldehyde dehydrogenase
YCR021CHSP306.05.37 × 10−3Negative regulator of the H(+)-ATPase Pma1p
YBR256CRIB55.91.15 × 10−3Riboflavin synthase
YOR052CTMC15.89.56 × 10−3AN1-type zinc finger protein of unknown function
YOL155CHPF15.86.09 × 10−5Haze-protective mannoprotein
YMR318CADH65.87.64 × 10−3NADPH-dependent medium chain alcohol dehydrogenase
YJL082WIML25.84.56 × 10−4Protein of unknown function
YKL051WSFK15.66.62 × 10−6Plasma membrane protein that may act to generate normal levels of PI4P
YER185WPUG15.63.14 × 10−5Plasma membrane protein involved in protoprophyrin and heme transport
YIR017CMET285.63.48 × 10−6Basic leucine zipper (bZIP) transcriptional activator in the Cbf1p-Met4p-Met28p complex
YHL024WRIM45.54.66 × 10−6Putative RNA-binding protein
YGR243WMPC35.47.07 × 10−5Highly conserved subunit of mitochondrial pyruvate carrier
YGL010WMPO15.37.58 × 10−6Protein involved in metabolism of phytosphingosine
YDR513WGRX25.16.09 × 10−3Cytoplasmic glutaredoxin
YHR179WOYE25.11.04 × 10−2Conserved NADPH oxidoreductase containing flavin mononucleotide (FMN)
YDR059CUBC55.12.39 × 10−4Ubiquitin-conjugating enzyme
YMR276WDSK25.05.01 × 10−3Nuclear-enriched ubiquitin-like polyubiquitin-binding protein
* Fold change (FC) refers to the fold induction of the genes as compared to the untreated control.
Table 2. Genes > 5-fold upregulated upon OTA (ochratoxin A) exposure.
Table 2. Genes > 5-fold upregulated upon OTA (ochratoxin A) exposure.
GeneStandard NameFC *p-ValueDescription
YER106WMAM160.22.77 × 10−8Monopolin
YGR225WAMA157.49.19 × 10−10Activator of meiotic anaphase promoting complex (APC/C)
YER179WDMC140.55.34 × 10−7Meiosis-specific recombinase
YOR298WMUM333.59.62 × 10−4Protein of unknown function
YFL011WHXT1033.21.38 × 10−7Putative hexose transporter
YLL046CRNP127.31.08 × 10−7Ribonucleoprotein
YER104WRTT10526.03.22 × 10−8Protein with a role in regulation of Ty1 transposition
YLR377CFBP123.31.62 × 10−7Fructose-1,6-bisphosphatase
YDR523CSPS122.76.27 × 10−6Putative protein serine/threonine kinase
YHR176WFMO120.21.11 × 10−5Flavin-containing monooxygenase
YBR040WFIG119.71.16 × 10−7Integral membrane protein
YGR059WSPR318.64.74 × 10−5septin protein involved in sporulation
YEL039CCYC716.96.54 × 10−7Cytochrome c isoform 2
YMR101CSRT116.73.73 × 10−7Forms the dehydrodolichyl diphosphate syntase (DDS) complex with NUS1
YDR218CSPR2814.11.11 × 10−6Meiotic septin
YDR256CCTA113.57.51 × 10−8Catalase A
YIL113WSDP113.32.62 × 10−7Stress-inducible dual-specificity MAP kinase phosphatase
YOL123WHRP112.91.98 × 10−6Subunit of cleavage factor I complex
YGL254WFZF112.62.03 × 10−7Transcription factor involved in sulfite metabolism
YPL201CYIG112.43.23 × 10−5Protein that interacts with glycerol 3-phosphatase
Q0275COX312.31.01 × 10−4Subunit III of cytochrome c oxidase (Complex IV)
YFL055WAGP312.32.34 × 10−6Low-affinity amino acid permease
YDR259CYAP611.41.88 × 10−5Basic leucine zipper (bZIP) transcription factor
YPR193CHPA211.32.74 × 10−5Tetrameric histone acetyltransferase
YOR378WAMF111.32.33 × 10−6Low affinity NH4+ transporter
YLL042CATG1011.33.47 × 10−6Conserved E2-like conjugating enzyme
YIL101CXBP111.13.43 × 10−4Transcriptional repressor
YBR018CGAL711.02.12 × 10−5Galactose-1-phosphate uridyl transferase
YEL019CMMS2110.96.11 × 10−6SUMO ligase and component of the SMC5-SMC6 complex
YPR040WTIP4110.93.19 × 10−5Protein that interacts with Tap42p
YPL033CSRL410.71.75 × 10−6Protein of unknown function
YLL057CJLP110.51.82 × 10−6Fe(II)-dependent sulfonate/alpha-ketoglutarate dioxygenase
YGR142WBTN210.32.34 × 10−5v-SNARE binding protein
YPL279CFEX210.32.64 × 10−7Protein involved in fluoride export
YHL022CSPO1110.22.70 × 10−7Meiosis-specific protein
YKL055COAR110.02.10 × 10−6Mitochondrial 3-oxoacyl-[acyl-carrier-protein] reductase
YNL009WIDP310.01.42 × 10−2Peroxisomal NADP-dependent isocitrate dehydrogenase
YOR297CTIM189.93.75 × 10−5Component of the mitochondrial TIM22 complex
YER053C-A-9.87.45 × 10−6Protein of unknown function
YPL027WSMA19.71.50 × 10−7Protein of unknown function
YBR074WPFF19.65.70 × 10−6Multi-spanning vacuolar membrane protease
YEL048CTCA179.62.14 × 10−7Component of transport protein particle (TRAPP) complex II
YGR197CSNG19.27.32 × 10−8Protein involved in resistance to nitrosoguanidine and 6-azauracil
YJR047CANB19.21.29 × 10−6Translation elongation factor eIF-5A
YKL093WMBR19.03.41 × 10−5Protein involved in mitochondrial functions and stress response
YGR212WSLI19.02.03 × 10−5N-acetyltransferase
YCL026C-AFRM28.81.66 × 10−6Type II nitroreductase
YEL072WRMD68.76.39 × 10−7Protein required for sporulation
YML054CCYB28.52.74 × 10−6Cytochrome b2 (l-lactate cytochrome-c oxidoreductase)
YNL187WSWT218.56.08 × 10−6Protein involved in mRNA splicing
YNR064C-8.51.99 × 10−5Epoxide hydrolase
YBR065CECM28.49.49 × 10−6Pre-mRNA splicing factor
YPL171COYE38.46.43 × 10−6Conserved NADPH oxidoreductase containing flavin mononucleotide (FMN)
YGL212WVAM78.41.02 × 10−4Vacuolar SNARE protein
YOR390WFEX18.23.59 × 10−6Protein involved in fluoride export
YMR069WNAT48.11.76 × 10−4N-alpha-acetyl-transferase
YDL020CRPN48.03.51 × 10−7Transcription factor that stimulates expression of proteasome genes
YDR171WHSP428.06.87 × 10−6Small heat shock protein (sHSP) with chaperone activity
YER054CGIP27.92.59 × 10−6Putative regulatory subunit of protein phosphatase Glc7p
YPR151CSUE17.99.84 × 10−7Protein required for degradation of unstable forms of cytochrome c
YGR131WFHN17.71.62 × 10−6Protein of unknown function
YEL061CCIN87.61.15 × 10−5Kinesin motor protein
YDR079WPET1007.64.29 × 10−6Chaperone that specifically facilitates the assembly of cytochrome c oxidase
YKL051WSFK17.61.38 × 10−4Plasma membrane protein
YMR017WSPO207.51.72 × 10−3Meiosis-specific subunit of the t-SNARE complex
YDR011WSNQ27.54.53 × 10−7Plasma membrane ATP-binding cassette (ABC) transporter
YOR152CATG407.44.01 × 10−5Autophagy receptor
YLR312CATG397.42.53 × 10−7Autophagy receptor
YBL078CATG87.37.40 × 10−7Component of autophagosomes and Cvt vesicles
YPL186CUIP47.24.47 × 10−4Protein that interacts with Ulp1p
YLR142WPUT17.12.11 × 10−6Proline oxidase
YOR065WCYT17.04.71 × 10−5Cytochrome c1
YOL149WDCP17.01.35 × 10−3Subunit of the Dcp1p-Dcp2p decapping enzyme complex
Q0250COX26.73.78 × 10−2Subunit II of cytochrome c oxidase (Complex IV)
YDR402CDIT26.61.08 × 10−3N-formyltyrosine oxidase
YGR243WMPC36.61.70 × 10−5Highly conserved subunit of the mitochondrial pyruvate carrier (MPC)
YOR005CDNL46.65.57 × 10−6DNA ligase
YJR010WMET36.69.83 × 10−7ATP sulfurylase
YLR151CPCD16.52.79 × 10−68-oxo-dGTP diphosphatase
YNL158WPGA16.34.04 × 10−4Essential component of GPI-mannosyltransferase II
YDR524CAGE16.38.02 × 10−7ADP-ribosylation factor (ARF) GTPase activating protein (GAP) effector
YNL012WSPO16.34.68 × 10−6Meiosis-specific prospore protein
YGL240WDOC16.36.44 × 10−5Processivity factor
YDR076WRAD556.31.32 × 10−4Protein that stimulates strand exchange
YOR192CTHI726.37.85 × 10−6Transporter of thiamine or related compound
YMR251WGTO36.32.35 × 10−5Omega class glutathione transferase
YDR185CUPS36.24.77 × 10−6Mitochondrial protein of unknown function
YNL014WHEF36.21.32 × 10−4Translational elongation factor EF-3
YML087CAIM336.21.01 × 10−4Putative protein of unknown function
YNR034WSOL16.27.19 × 10−7Protein with a possible role in tRNA export
YDR070CFMP166.13.24 × 10−4Protein of unknown function
YJR129CEFM36.14.06 × 10−2S-adenosylmethionine-dependent methyltransferase
Q0045COX16.01.76 × 10−2Subunit I of cytochrome c oxidase (Complex IV)
YNL036WNCE1035.94.88 × 10−5Carbonic anhydrase
YOR178CGAC15.96.08 × 10−4Regulatory subunit for Glc7p type-1 protein phosphatase (PP1)
YGR088WCTT15.98.13 × 10−5Cytosolic catalase T
YDL247WMPH25.82.28 × 10−5Alpha-glucoside permease
YCL066WHMLALPHA15.76.90 × 10−4Silenced copy of ALPHA1 at HML
YNL077WAPJ15.63.33 × 10−6Chaperone with a role in SUMO-mediated protein degradation
YKL095WYJU25.61.29 × 10−3Essential protein required for pre-mRNA splicing
YJL030WMAD25.61.64 × 10−4Component of the spindle-assembly checkpoint complex
YHL016CDUR35.69.87 × 10−7Plasma membrane transporter for urea and polyamines
YNL188WKAR15.61.64 × 10−4Protein involved in karyogamy and spindle pole body duplication
YGR234WYHB15.61.02 × 10−5Nitric oxide oxidoreductase
YCR040WMATALPHA15.56.76 × 10−4Transcriptional co-activator that regulates mating-type-specific genes
YFL016CMDJ15.52.05 × 10−4Co-chaperone that stimulates HSP70 protein Ssc1p ATPase activity
YNL194C-5.44.89 × 10−4Integral membrane protein
YDR475CJIP45.32.01 × 10−3Protein of unknown function
YJR160CMPH35.38.87 × 10−5Alpha-glucoside permease
YCR104WPAU35.31.92 × 10−3Member of the seripauperin multigene family
YIL084CSDS35.36.30 × 10−6Component of the Rpd3L histone deacetylase complex
YIL056WVHR15.13.53 × 10−3Transcriptional activator
YAR020CPAU75.01.56 × 10−4Member of the seripauperin multigene family
YDR227WSIR45.01.71 × 10−5Silent information regulator
YLR376CPSY35.06.70 × 10−6Component of Shu complex (aka PCSS complex)
* Fold change (FC) refers to the fold induction of the genes as compared to the untreated control.
Table 3. Genes > 5-fold upregulated upon the combined CIT/OTA exposure.
Table 3. Genes > 5-fold upregulated upon the combined CIT/OTA exposure.
GeneStandard NameFC *p-ValueDescription
YPL171COYE3199.61.29 × 10−4Conserved NADPH oxidoreductase containing flavin mononucleotide (FMN)
YDL243CAAD446.51.49 × 10−9Putative aryl-alcohol dehydrogenase
YFL056CAAD641.21.16 × 10−7Putative aryl-alcohol dehydrogenase
YLL060CGTT234.61.44 × 10−9Glutathione S-transferase capable of homodimerization
YBR008CFLR128.01.21 × 10−7Plasma membrane transporter of the major facilitator superfamily
YML131W-24.22.41 × 10−6Protein of unknown function
YOL151WGRE221.91.17 × 10−43-methylbutanal reductase and NADPH-dependent methylglyoxal reductase
YCL026C-AFRM221.51.53 × 10−8Type II nitroreductase
YMR101CSRT121.32.64 × 10−8Forms the dehydrodolichyl diphosphate syntase (DDS) complex with NUS1
YGR225WAMA120.53.87 × 10−7Activator of meiotic anaphase promoting complex (APC/C)
YDL020CRPN419.54.24 × 10−4Transcription factor that stimulates expression of proteasome genes
YDR256CCTA118.84.53 × 10−9Catalase A
YGR197CSNG118.75.35 × 10−9Protein involved in resistance to nitrosoguanidine and 6-azauracil
YKL051WSFK118.76.62 × 10−8Plasma membrane protein that may act to generate normal levels of PI4P
YML116WATR116.39.44 × 10−6Multidrug efflux pump of the major facilitator superfamily
YGR142WBTN215.27.12 × 10−6v-SNARE binding protein
YHR087WRTC315.01.01 × 10−6Protein of unknown function involved in RNA metabolism
YDR406WPDR1514.23.31 × 10−6Plasma membrane ATP binding cassette (ABC) transporter
YFL057CAAD1613.71.51 × 10−5Putative aryl-alcohol dehydrogenase
YOL149WDCP113.53.61 × 10−5Subunit of the Dcp1p-Dcp2p decapping enzyme complex
YDR171WHSP4213.51.19 × 10−3Small heat shock protein (sHSP) with chaperone activity
YIL101CXBP112.33.01 × 10−5Transcriptional repressor
YHR139CSPS10012.31.95 × 10−7Protein required for spore wall maturation
YGR213CRTA112.11.04 × 10−8Protein involved in 7-aminocholesterol resistance
YEL039CCYC711.84.14 × 10−8Cytochrome c isoform 2
YIL056WVHR110.54.95 × 10−7Transcriptional activator
YCL026C-BHBN110.58.33 × 10−6Protein of unknown function
YOL123WHRP110.42.81 × 10−6Subunit of cleavage factor I
YHL036WMUP39.56.44 × 10−7Low affinity methionine permease
YKR076WECM49.44.12 × 10−7Omega class glutathione transferase
YLR108C-9.13.50 × 10−7Protein of unknown function
YER054CGIP28.91.55 × 10−7Putative regulatory subunit of protein phosphatase Glc7p
YOR298WMUM38.93.49 × 10−6Protein of unknown function involved in outer spore wall organization
YHL024WRIM48.64.31 × 10−8Putative RNA-binding protein
YMR169CALD38.36.99 × 10−3Cytoplasmic aldehyde dehydrogenase
YOR028CCIN58.22.47 × 10−7Basic leucine zipper (bZIP) transcription factor of the yAP-1 family
YGR088WCTT18.13.34 × 10−6Cytosolic catalase T
YER103WSSA48.01.02 × 10−5Heat shock protein member of the HSP70 family
YER185WPUG17.51.07 × 10−5Plasma membrane protein involved in protoprophyrin and heme transport
YER053C-A-7.21.56 × 10−4Protein of unknown function
YOR152CATG407.23.92 × 10−5Autophagy receptor
YDL204WRTN26.71.74 × 10−6Reticulon protein
YOR065WCYT16.64.43 × 10−6Cytochrome c1
YJL051WIRC86.65.68 × 10−5Bud tip localized protein of unknown function
YLR329WREC1026.54.83 × 10−6Protein involved in early stages of meiotic recombination
YKR077WMSA26.46.97 × 10−6Putative transcriptional activator
YHR138C-6.17.19 × 10−3Protein of unknown function
YPL201CYIG16.04.46 × 10−7Protein that interacts with glycerol 3-phosphatase
YDL025CRTK16.03.61 × 10−2Putative protein kinase
YOR178CGAC15.99.69 × 10−4Regulatory subunit for Glc7p type-1 protein phosphatase (PP1)
YFL016CMDJ15.84.14 × 10−5Co-chaperone member of the HSP40 (DnaJ) family of chaperones
YFL030WAGX15.81.51 × 10−6Alanine:glyoxylate aminotransferase (AGT)
YKL086WSRX15.85.28 × 10−5Sulfiredoxin
YOR328WPDR105.81.96 × 10−6ATP-binding cassette (ABC) transporter
YPR151CSUE15.61.71 × 10−7Protein required for degradation of unstable forms of cytochrome c
YLL026WHSP1045.54.85 × 10−2Disaggregase
YGR243WMPC35.55.30 × 10−5Highly conserved subunit of the mitochondrial pyruvate carrier (MPC)
YKL093WMBR15.52.19 × 10−5Protein involved in mitochondrial functions and stress response
YNL036WNCE1035.55.13 × 10−5Carbonic anhydrase
YNL008CASI35.51.69 × 10−5Subunit of the nuclear inner membrane Asi ubiquitin ligase complex
YLR343WGAS25.54.37 × 10−61,3-beta-glucanosyltransferase
YGR223CHSV25.41.69 × 10−6Phosphatidylinositol 3,5-bisphosphate-binding protein
YER060W-AFCY225.21.17 × 10−5Putative purine-cytosine permease
YNL155WCUZ15.21.90 × 10−3Protein with a role in the ubiquitin-proteasome pathway
YHL021CAIM175.21.36 × 10−4Putative protein of unknown function
YHR199CAIM465.21.08 × 10−5Putative protein of unknown function
YGR281WYOR15.12.18 × 10−3Plasma membrane ATP-binding cassette (ABC) transporter
YGL010WMPO15.13.53 × 10−6Protein involved in metabolism of phytosphingosine
* Fold change (FC) refers to the fold induction of the genes as compared to the untreated control.
Table 4. Functional gene groups induced by the separated or combined exposure to CIT and OTA.
Table 4. Functional gene groups induced by the separated or combined exposure to CIT and OTA.
CITp-value
Gene Ontology Group
Oxidation-reduction process1.8 × 10−13
Cell response to oxidative stress2.2 × 10−9
Glutathione metabolic process1.8 × 10−6
Drug transport1.3 × 10−5
Response to reactive oxygen species1.3 × 10−4
OTAp-value
Gene Ontology Group
Single organism developmental process2.2 × 10−8
Oxidation-reduction process2.0 × 10−7
Cell differentiation3.0 × 10−6
Developmental process involved in reproduction5.4 × 10−6
Sporulation1.6 × 10−5
Cell response to oxidative stress5.4 × 10−3
CIT + OTAp-value
Gene Ontology Group
Oxidation-reduction process1.7 × 10−7
Drug transport1.3 × 10−5
Cell response to oxidative stress3.1 × 10−4
Spore wall assembly1.4 × 10−3
Single organism developmental process4.2 × 10−3

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MDPI and ACS Style

Vanacloig-Pedros, E.; Proft, M.; Pascual-Ahuir, A. Different Toxicity Mechanisms for Citrinin and Ochratoxin A Revealed by Transcriptomic Analysis in Yeast. Toxins 2016, 8, 273. https://doi.org/10.3390/toxins8100273

AMA Style

Vanacloig-Pedros E, Proft M, Pascual-Ahuir A. Different Toxicity Mechanisms for Citrinin and Ochratoxin A Revealed by Transcriptomic Analysis in Yeast. Toxins. 2016; 8(10):273. https://doi.org/10.3390/toxins8100273

Chicago/Turabian Style

Vanacloig-Pedros, Elena, Markus Proft, and Amparo Pascual-Ahuir. 2016. "Different Toxicity Mechanisms for Citrinin and Ochratoxin A Revealed by Transcriptomic Analysis in Yeast" Toxins 8, no. 10: 273. https://doi.org/10.3390/toxins8100273

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