- Research article
- Open Access
Identification of possible targets of the Aspergillus fumigatus CRZ1 homologue, CrzA
© Sorian et al; licensee BioMed Central Ltd. 2010
- Received: 30 March 2009
- Accepted: 15 January 2010
- Published: 15 January 2010
Calcineurin, a serine/threonine-specific protein phosphatase, plays an important role in the control of cell morphology and virulence in fungi. Calcineurin regulates localization and activity of a transcription factor called CRZ1. Recently, we characterize Aspergillus fumigatus CRZ1 homologue, AfCrzA. Here, we investigate which pathways are influenced by A. fumigatus AfCrzA during a short pulse of calcium by comparatively determining the transcriptional profile of A. fumigatus wild type and ΔAfcrzA mutant strains.
We were able to observe 3,622 genes modulated in at least one timepoint in the mutant when compared to the wild type strain (3,211 and 411 at 10 and 30 minutes, respectively). Decreased mRNA abundance in the ΔcrzA was seen for genes encoding calcium transporters, transcription factors and genes that could be directly or indirectly involved in calcium metabolism. Increased mRNA accumulation was observed for some genes encoding proteins involved in stress response. AfCrzA overexpression in A. fumigatus increases the expression of several of these genes. The deleted strain of one of these genes, AfRcnA, belonging to a class of endogenous calcineurin regulators, calcipressins, had more calcineurin activity after exposure to calcium and was less sensitive to menadione 30 μM, hydrogen peroxide 2.5 mM, EGTA 25 mM, and MnCl2 25 mM. We constructed deletion, overexpression, and GFP fusion protein for the closely related A. nidulans AnRcnA. GFP::RcnA was mostly detected along the germling, did not accumulate in the nuclei and its location is not affected by the cellular response to calcium chloride.
We have performed a transcriptional profiling analysis of the A. fumigatus ΔAfcrzA mutant strain exposed to calcium stress. This provided an excellent opportunity to identify genes and pathways that are under the influence of AfCrzA. AfRcnA, one of these selected genes, encodes a modulator of calcineurin activity. Concomitantly with A. fumigatus AfrcnA molecular analysis, we decided to exploit the conserved features of A. nidulans calcineurin system and investigated the A. nidulans AnRcnA homologue. A. nidulans AnRcnA mutation is suppressing CnaA mutation and it is responsible for modulating the calcineurin activity and mRNA accumulation of genes encoding calcium transporters.
- mRNA Accumulation
- Calcium Stress
The phosphatase calcineurin is a heterodimeric protein composed by a catalytic subunit A and a regulatory subunit B . In fungi, calcineurin plays an important role in the control of cell morphology and virulence [1–4]. Calcineurin regulates morphogenesis, Ca+2 homeostasis, and stress-activated transcription in Saccharomyces cerevisiae [1, 5]. In pathogenic fungi, calcineurin affects virulence, morphogenesis, and antifungal drug action [1, 6–9]. Inactivation of calcineurin in Cryptococcus neoformans affects growth at 37°C and hyphal elongation during mating and haploid fruiting [10–13]. Reduced virulence and absence of growth in serum are also observed in Candida albicans depleted in the calcineurin activity [11, 14, 15]. In A. fumigatus, calcineurin inactivation decreases the virulence and provides decreased filamentation and no growth in serum [9, 16].
Calcineurin regulates the localization and activity of the transcription factor Crz1p by dephosphorylating it . Upon increase in cytosolic calcium, calcineurin dephosphorylates Crz1p, allowing its nuclear translocation [17, 18]. Crz1p has a C2H2 zinc finger motif that binds to a CDRE (c alcineurin-d ependent r esponse e lement) in the promoters of genes that are regulated by calcineurin and calcium . Mutants of S. cerevisiae inactivated in CRZ1 display hypersensitivity to chloride and chitosan, a defective transcriptional response to alkaline stress, and cellular morphology and mating defects [17, 19–21]. Inactivation CRZ1 mutants of Schizosaccharomyces pombe (Δprz1) are hypersensitive to calcium and have decreased transcription of the Pmc1 Ca+2 pump . C. albicans homozygotes crz1Δ/Δ are moderately attenuated for virulence and sensitive to calcium, lithium, manganese, and sodium dodecyl sulfate [18, 23, 24]. A. fumigatus CRZ1 mutant, ΔcrzA, is avirulent and has decreased conidiation [16, 25]. Its hypersensitivity to calcium and manganese is probably due to the reduced expression of calcium transporter mRNAs under high concentrations of calcium .
Here, we investigate which pathways are influenced by A. fumigatus AfCrzA during a short pulse of calcium by comparatively determining the transcriptional profile of A. fumigatus wild type and ΔAfcrzA mutant strains. Our results revealed several possible novel targets for AfCrzA, including AfRcnA, a member of the conserved calcineurin-binding proteins, the calcipressins. Besides the transcriptional profiling of the A. fumigatus ΔAfcrzA, we also showed the molecular characterization of Aspergilli RcnAs.
Transcriptional profiling of the A. fumigatus ΔcrzA mutant strain
To have a better understanding of which genes are influenced by A. fumigatus AfCrzA during exposure to calcium, we performed competitive microarray hybridizations using RNA obtained from the wild type and ΔAfcrzA strains after short pulses (10 and 30 minutes) of 200 mM calcium chloride. RNA obtained from wild type mycelia exposed to 10 and 30 minutes calcium was taken as reference. Thus, total RNA extracted from these cultures was used to synthesize fluorescent-labeled cDNAs for competitive microarray hybridizations. In these experiments, the main aim was to focus on genes that have increased or decreased mRNA expression in the absence of AfCrzA. We were able to observe 3,622 genes modulated in at least one timepoint in the mutant when compared to the wild type strain (3,211 and 411 at 10 and 30 minutes, respectively). The large difference between the number of genes modulated at 10 and 30 minutes (about eight-times more at 10 minutes) suggests A. fumigatus responds rapidly to calcium stressing conditions. The full dataset was deposited in the Gene Expression Omnibus (GEO) from the National Center of Biotechnology Information (NCBI) with the number GSE15432 http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/projects/geo/query/acc.cgi?acc=GSE15432. Previously, to evaluate the effect of calcium on global A. fumigatus gene expression, we performed competitive microarray hybridizations using RNA obtained from the wild type strain before and after a short pulse (10 minutes) of 200 mM calcium chloride (Soriani et al., 2008). Statistical analysis of this dataset identified a total of 863 genes that displayed modulation. The large difference in genes whose expression is modulated between this dataset and the current dataset using a comparison between ΔcrzA and the wild type strains emphasizes the pleiotropic role played by A. fumigatus calcineurin-CrzA in the calcium-mediated signal transduction pathways. We are currently investigating the importance of this difference.
We observed differential regulation of genes involved in a variety of cellular processes and specific modulation of these functions is therefore likely to be implicated with A. fumigatus adaptation to high concentrations of calcium (Additional files 1 and 2, Tables S1 and S2, respectively, show the genes with log ratios more than or equal to 1 or less than or equal to 1 in at least in one time point, respectively). These genes were classified into COG functional categories http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/COG/. However, we were not able to observe any significant enrichment for a specific COG category (Additional files 1 and 2, Tables S1 and S2, repectively). We noted decreased mRNA abundance in the ΔAfcrzA of several genes involved in calcium transport, such as the vacuolar H+/Ca+2 (Afu2g07630), calcium-translocating P-type ATPase (PMCA-type, Afu3g10690), and calcium-transporting ATPase 1 (PMC1, Afu7g01030). We also observed decreased mRNA accumulation when the ΔAfcrzA strain was exposed to calcium of genes encoding several transcription factors [CtfA (Afu4g03960), RfeF (Afu4g10200), and ZfpA (Afu8g05010)], and genes that could be directly or indirectly involved in calcium metabolism [such as a phospholipase D (Afu2g16520), two peptidyl-prolyl cis-trans isomerases (Afu5g13350 and Afu2g03720), a calcineurin binding protein (Afu2g13060), a Bar adaptor protein (Afu3g14230), and a potential regulator of cytoskeleton and endocytosis, homologue of mammalian amphiphysin. Interestingly, a chitin synthase A (Afu2g01870) also showed decreased mRNA accumulation in the ΔAfcrzA strain background. Cramer et al.  have shown that the calcineurin pathway plays an important role in cell wall biosynthesis in A. fumigatus, and that calcineurin and AfCrzA inactivation mutants are more sensitive to specific cell wall inhibitors, such as caspofungin. However, in contrast to our results these authors have observed an increased and decreased mRNA accumulation of chitin synthase A in the ΔAfcrzA and ΔAfcalA mutant strains, respectively. Several of the genes above mentioned (such as Afu2g16520, Afu2g13060, Afu3g14230, Afu4g10200, Afu8g05010, and Afu3g10690) have also been observed by Soriani et al.  as more expressed upon exposure of A. fumigatus to calcium. We have also previously observed that zfpA (Afu8g01050) has increased mRNA accumulation that is dependent on the cyclic AMP-protein kinase A signaling pathway during adaptation to voriconazole . Thus, it is plausible that zfpA is related to a transcriptional network controlled by calcineurin-CrzA that has a key role in mediating cellular stress responses.
We observed increased mRNA accumulation when the ΔAfcrzA strain was exposed to calcium of genes encoding a class V chitinase (Afu7g08490), an exo-β-1,3-glucanase (Afu2g00430), an AAA family ATPase (Afu4g04800), a cation diffusion facilitator 3, a multidrug resistance protein (Afu4g01140), a TOR signalling pathway protein TipA (Afu2g07540), an inositol polyphosphate phosphatase (Afu5g02140), a representative of the Hsp9-12 heat shock protein Scf1 (Afu1g17370), and a protein phosphatase 2C (Afu4g00720). Again, the increased expression of the chitinase and exo-β-1,3-glucanase could help to explain the increased sensitivity of A. fumigatus ΔAfcrzA strain to caspofungin . Interestingly, some of these genes are involved in stress response, such as: (i) the Scf1 homologue (Afu117370), a plasma membrane localized protein that protects membranes from desiccation and it is induced by heat shock, oxidative stress, osmostress, stationary phase entry, glucose depletion, oleate and alcohol, and is regulated by the HOG and Ras-Pka pathways http://www.yeastgenome.org; (ii) TipA (Afu2g07540), a component of the TOR (target of rapamycin) signaling pathway, that interacts physically and genetically with Tap42p, which regulates protein phosphatase 2A ; and (iii) a protein phosphatase 2C (Afu4g00720), important physiological regulator of cell growth and of cellular stress signaling . The increased mRNA accumulation of these genes could mean that they are directly or indirectly repressed by AfCrzA and can open new frontiers for studying biochemical pathways that are under influence of the A. fumigatus calcineurin-CrzA pathway.
It is very impressive the mRNA accumulation levels of the Hsp9-12 heat shock protein Scf1 homologue (Afu1g17370): about 100 and 1000 times more in the ΔcrzA and ΔcalA than in the wild type, respectively (Figure 1E). A. fumigatus has two Hsp12 homologues, Afu1g17370 (e-value = 3.7e-10; 45 and 57 identity and similarity, respectively) and Afu6g12450 (e-value = 3.1e-9; 39 and 56 identity and similarity, respectively). Interestingly, the S. cerevisiae HSP12 was also shown to be induced by calcium but in contrast to the A. fumigatus homologue, the S. cerevisiae gene is repressed when calcium+FK506 were added and accordingly repressed in the ΔCRZ1 background . Thus, it remains to be determined the roles played by calcineurin, AfCrzA, and AfHsp12p during adaptation of A. fumigatus to calcium stress.
Recently, Hagiwara et al.  identified and characterized the A. nidulans AncrzA gene. They performed an in silico analysis by using MEME (Motif-based sequence analysis tools; http://meme.sdsc.edu/meme4_1_1/intro.html) of the possible presence of a CDRE-like consensus motif in the promoter regions of 25 AnCrzA-dependent genes. By analyzing their promoter regions, 5'-G[T/G]GGC[T/A]G[T/G]G-3' was presumed to be the consensus sequence for the A. nidulans AnCrzA-dependent genes. By using a combination of MEME analysis and the A. nidulans CDRE consensus as a guide, we were able to identify in the AfrcnA, AfrfeF, AfBAR, and the A. fumigatus phospholipase D promoter regions (about 500 bp upstream ATG) the following CDRE motifs: (i) AfrcnA (5'-GTTGGTGAG-3', -314 bp upstream ATG starting point), (ii) AfrfeF (5'GTGGCTGAT-3', -184 bp upstream ATG), (iii) AfBAR (5'-GTGGCTGAC-3', -309 bp upstream ATG), and (iv) A. fumigatus phospholipase D (5'-GTTGGAGAG-3', -239 upstream ATG). We compared these motifs with the promoter regions (about 500 bp upstream ATG) of 32 repressed genes described in Additional file 1, Table S1, and this analysis suggested 5'-GT[T/G]G[G/C][T/A]GA[G/T]-3' as the CDRE-consensus sequence for A. fumigatus AfCrzA-dependent genes. We also analyzed Afscf1 and Af AAA ATPase genes and found the following CDRE-like motifs: (i) Afscf1 (5'-GGGAACGAA-3', -376 bp upstream ATG), and (ii) Af AAA ATPase (5'-GAAGACGAG-3', -19 bp upstream ATG). Again, we compared these motifs with the promoter regions (about 500 bp upstream ATG) of 109 induced genes described in Additional file 2, Table S2, and we were able to propose as a putative CDRE consensus for gene repressed by AfCrzA, the sequence 5'-G[A/G][A/G][A/G]ACGA[A/G]-3'. It remains to be experimentally determined if these sequences are really important for AfCrzA gene regulation, both for gene induction and repression.
Prior to this work, a study analysing global gene expression regulated by the calcineurin/Crz1p signaling pathway in S. cerevisiae had attempted to identify genes regulated by calcium and sodium . Calcineurin activation induced 153 genes involved in cell wall biosynthesis, ion homeostasis, vesicle trafficking, lipid synthesis, and protein degradation. A notable similarity was observed by the authors in the gene expression patterns of FK506-treated cells and crz1 cells, suggesting that Crz1p is required for most calcineurin-dependent changes in gene expression. Recently, Soriani et al.  opted to an alternative strategy, exposing A. fumigatus wild type strain to a short pulse with a high concentration of calcium, and arbitrarily choosing several genes that were less or more expressed in the microarray hybridization analyses to verify their expression in the wild type, and ΔAfcalA and ΔAfcrzA mutant strains by real-time RT-PCR. Thus, these authors were able to determine if the expression of these genes was dependent on calcineurin and/or AfCrzA. They verified that the majority of these genes suffered blocking of mRNA accumulation in the ΔAfcrzA background. The results shown here added more information about the transcriptional network involved in the calcineurin-AfCrzA in response to calcium.
Construction of Aspergilli CrzA overexpression strains
A. fumigatus AfRcnA belongs to a class of endogenous calcineurin regulators, calcipressins, a family of calcineurin-binding proteins, conserved from yeast to mammals [34, 35]. A phylogenetic analysis was performed to determine the relationship of AfRcnA to calcipressin homologues in several different organisms (Additional file 3, Figure S1). The mechanism how this protein family functions still remains controversial. There are reports showing that calcipressins can both stimulate and inhibit the calcineurin pathway 343536. Induction of S. cerevisiae RCN1-lacZ in response to calcium was completely blocked by addition of FK506 or by deletion of the genes encoding Tcn1p or calcineurin . The S. cerevisiae RCN1 is also induced by calcium, repressed by calcium+FK506 and in the crz1 background . Another member of this family, Cbp1, was identified in Cryptococcus neoformans, and is required for mating but not for growth at 37°C . We have observed that AfrcnA mRNA accumulation upon calcium stress is dependent on both calcineurin and AfCrzA (Figure 1A). These results suggest that both S. cerevisiae and A. fumigatus RCAN homologues may be downstream targets of the calcineurin-dependent transcription factor. This fits a model where increased A. fumigatus AfRcnA regulation in response to calcineurin signaling is possibly a negative-feedback mechanism modulating calcineurin acitivity.
We constructed an A. nidulans alcA::AncrzA also by replacing the endogenous AncrzA promoter region homologously with the A. nidulans alcA promoter. We investigate the genetic interactions between ΔAncnaA and ΔAncrzA mutations and a double mutant ΔAncnaA ΔAncrzA displays the same growth behavior than the ΔAncnaA mutant indicating as expected that AncnaA is epistatic to AncrzA (data not shown).
Molecular characterization of the Aspergilli calcipressin homologue
The first member identified from the calcipressin family, RCAN1, was isolated from the hamster genome as a gene induced during transient adaptation to oxidative stress [42, 43]. It was observed that resistance to oxidative stress and calcium stress increased as a function of RCAN1 expression and decreased as its expression diminished . Porta et al.  have shown that RCAN1 mRNA and protein expression are sensitive to oxidative stress in primary neurons, and that Rcan1 -/- neurons display an increased resistance to damage by hydrogen peroxide. Taken together, our results suggest that Aspergilli RcnA play a role in calcium and oxidative stress signaling.
Next step, we crossed the A. nidulans ΔAnrcnA strain with ΔAncnaA strain (cnaA encodes the catalytic subunit of the calcineurin gene) . The A. nidulans ΔAnrcnA mutation can partially suppress the ΔAncnaA growth defect, suggesting a genetic interaction between AnRcnA and AnCnaA (Figure 6C). To determine the AnRcnA cellular localization, we transformed a GFP::AnRcnA cassette into a wild type strain. Several transformants were obtained in which the plasmid had integrated homologously at the AnrcnA locus (data not shown). Thus, in these strains GFP::AnRcnA is the only source of protein and GFP::AnRcnA strains are completely functional, i.e., they displayed cyclosporine A/paraquat-sensitivity comparable to the wild type strain (data not shown). Figure 6D shows GFP::AnRcnA germlings that were grown for 24 hs in MM+2% glycerol at 30°C and either incubated or not in the presence of calcium chloride 50 mM or EGTA 25 mM for 5 to 15 minutes. In all conditions, AnRcnA was mostly detected along the germling and did not accumulate in the nuclei (Figure 6D and data not shown). The same results were observed when glucose was used as a single carbon source (data not shown). These results show that AnRcnA cellular localization is not affected by the cellular response to calcium chloride.
We investigated the effects of AnRcnA overexpression on the mRNA accumulation of the calcium transporters pmcA (AN1189.3) and pmcB (AN4920.3), two A. nidulans PMC1 homologues. Low and about similar pmcA and pmcB mRNA accumulation were seen when the wild type and the alcA::AnrcnA mutant strains were grown in the presence of glucose (Figure 7C). In contrast, pmcA and pmcB levels were about 16 and 5 times higher the alcA::AnrcnA strain than in the wild type when both strains were grown in the presence of glycerol+ethanol (Figure 7C). These results strongly suggest that AnRcnA can directly or indirectly influence the pmcA and pmcB mRNA accumulation. Thus, it is possible RcnA has both stimulatory and inhibitory activity depending on the calcineurin pathway activation by calcium stress.
Taken together, these results strongly suggest that: (i) rcnA genes are involved in the oxidative stress and calcium stress in Aspergilli, (ii) both AncnaA and AnrcnA genes showed genetic interactions, and (iii) RcnA can modulate calcineurin activity and the mRNA accumulation of genes encoding calcium transporters. What is the nature of the interaction between Aspergilli CnaA and RcnA? These interactions could mean protein-protein interactions, and considering that calcipressin homologues from other species were already shown to interact with calcineurin 3545, we investigated the possibility of AfRcnA to bind AfCnaA by using yeast two-hybrid analysis. Our results have not revealed any even weak interaction between these two proteins (data not shown), suggesting that the basis for the interaction is either not related to protein-protein interaction or alternatively there are other proteins or conditions that mediate this interactions that cannot be completely recapitulated by using yeast two-hybrid assays. The ΔAnrcnA mutation suppresses the ΔAncnaA mutation and suppression of a null allele is expected to be due to downstream mutations that activate the pathway independent of the original (suppressed) gene product . This suppression is essentially visible in terms of the recovery of the colonial growth and increase in the radial diameter of the double mutant (see Figure 5C). Considering the dramatic morphological phenotype of ΔAncnaA strain, it is possible that besides controlling calcineurin activity, AnRcnA is also involved in Aspergillus development. Involvement of calcipressins in development has been previously reported for the Drosophila melanogaster sarah mutants . Eggs laid by sarah mutant females arrest in anaphase of meiosis I and fail to fully polyadenylate and translate bicoid mRNA. Furthermore, sarah mutant eggs show elevated cyclin B levels, indicating a failure to inactivate M-phase promoting factor (MPF). Taken together, these results demonstrate that calcium signaling is involved in Drosophila egg activation. It remains to be determined the further involvement of AnRcnA in A. nidulans development.
During the writing of this paper, a complementary study reporting the construction of the ΔAfrcnA mutant in the A. fumigatus strain AF293 was published (named CbpA) . These authors observed that deletion of the cbpA gene resulted in reduced hyphal growth and limited attenuated virulence. Different from our results, they also observed that the ΔcbpA strain showed increased calcium tolerance compared to the wild-type strain. Some differences between ours and their results can be credited to A. fumigatus strain differences. However, it is interesting to emphasize the fact that both Aspergilli showed some differences in the susceptibilities to manganese and EGTA (A. fumigatus) and cyclosporine A (A. nidulans). In contrast, those authors have shown that the A. fumigatus AF293 ΔcbpA and wild-type strains displayed an equal sensitivity to the oxidants menadione and hydrogen peroxide, and were also not able to demonstrate a direct protein-protein interaction between A. fumigatus CbpA and AfCnaA .
We have performed a transcriptional profiling analysis of the A. fumigatus ΔAfcrzA mutant strain exposed to calcium stress. This provided an excellent opportunity to identify genes and pathways that are under the influence of AfCrzA. We validated the relationship between AfCrzA and these selected genes by using deletion analysis and by checking through real-time RT-PCR the mRNA accumulation of these genes expressed either in the ΔAfcrzA or overexpression strains. AfRcnA, one of these selected genes, encodes a modulator of calcineurin activity. Recently, we demonstrated that contrary to previous findings, the gene encoding the A. nidulans calcineurin catalytic subunit homologue, AncnaA, is not essential and that the AncnaA deletion mutant shares the morphological phenotypes observed in the corresponding A. fumigatus mutant, ΔcalA . Thus, we decided once more to exploit the conserved features of A. nidulans calcineurin system and concomitantly with A. fumigatus AfrcnA molecular analysis, we investigated the A. nidulans AnRcnA homologue. AnRcnA showed to interact genetically with AnCnaA and be responsible for modulating the calcineurin activity and mRNA accumulation of genes encoding calcium transporters.
In summary, our work opens exciting new avenues for research into environmental sensing and nutrient acquisition mediated by the calcineurin-CrzA pathway in this important human pathogen.
Strains and media methods
A. fumigatus strains used in this study are CEA17 (pyrG-), CEA17-80 (wild type), ΔcalA , FMS5 (ΔcrzA::pyrG) , ALCCRZA (alcA::crzA), and RCNA (ΔrcnA). A. nidulans strains used are GR5 (pyroA4 pyrG89; wA3), TNO2a3 (pyroA4 pyrG8 ΔnKUa::argB) , CNA1 (ΔcnaA::pyroA; pyroA4 pyrG89; wA3) , ALCRZA1 (pyroA4, alcA::gfp::crzA), RCNA1 (pyroA4, ΔrcnA::pyrG), and ALCARCNA (pyroA4, alcA::gfp::rcnA). Media were of two basic types. A complete medium with three variants: YAG (2% glucose, 0.5% yeast extract, 2% agar, trace elements), YUU (YAG supplemented with 1.2 g/l each of uracil and uridine) and liquid YG or YG + UU medium of the same compositions (but without agar). A modified minimal medium (MM: 1% glucose, original high nitrate salts, trace elements, 2% agar, pH 6.5) was also used. Trace elements, vitamins, and nitrate salts are described by Kafer . Expression of tagged genes under the control of alcA promoter was regulated by carbon source: repression on glucose 4% (w/v), derepression on glycerol and induction on ethanol or threonine. Therefore, MM-G and MM-E (or MM-T) were identical to MM, except that glycerol (2% v/v) and/or ethanol (2% v/v for liquid medium) or threonine (100 mM for solid medium) were used, respectively, in place of glucose as the sole carbon source. Strains were grown at 37°C unless indicated otherwise. Cyclosporine A (CsA) used in the experiments throughout the manuscript is from Neoral™ Sandimmun (Novartis). Standard genetic techniques for A. nidulans were used for all strain constructions .
For the microarray experiments, 1.0 × 109 conidia of A. fumigatus wild type and ΔcrzA strains were used to inoculate 400 ml liquid cultures (YG) in 1000 ml erlenmeyer flasks that were incubated in a reciprocal shaker (250 rpm) at 37°C for 16 hours. After this period, the germlings were harvested by filtration and transferred to a fresh YG medium plus 200 mM of CaCl2 for either 10 or 30 minutes. Again, after this period, the germlings were harvested by centrifugation or filtration immediately frozen in liquid nitrogen. For total RNA isolation, the germlings were disrupted by grinding in liquid nitrogen with pestle and mortar and total RNA was extracted with Trizol reagent (Invitrogen, USA). Ten micrograms of RNA from each treatment were then fractionated in 2.2 M formaldehyde, 1.2% w/v agarose gel, stained with ethidium bromide, and then visualized with UV-light. The presence of intact 25S and 17S ribosomal RNA bands was used as a criterion to assess the integrity of the RNA. RNAse free DNAse I treatment for the real-time RT-PCR experiments was carried out as previously described .
Assay for calcineurin activity
Cytoplasmic extracts were prepared by homogenizing the mycelia using liquid nitrogen in a buffer containing 50 mM Tris-HCl, pH7.4, 1 mM EGTA, 0.2% Triton X-100, 1 mM benzamidine, and 10 g/ml each of leupeptin, pepstatin and aprotinine. The homogenates were clarified by centrifugation at 10,000 × g for 10 min at 4°C and then at 20,800 × g for 60 min at 4°C. Protein content in the extracts was determined by the method of Bradford  and then used for calcineurin activity assays. Calcineurin activity in the cytoplasmic extracts was assayed according to the method of Wang and Pallen , with minor modifications, by determining calmodulin-dependent protein phosphatase activity in the absence or in the presence of the inhibitor CsA (5 mM). CsA is an immunosuppressant that targets calcineurin by forming a molecular complex with cytosolic protein cyclophilin of immunocompetent lymphocytes, especially T-lymphocytes. This complex of CsA and cyclophylin inhibits its phosphatase activity. Assays were performed in a reaction mixture (100- l volume) containing 25 mM Tris (pH 7.2), 25 mM MES (pH 7.0), 5 mM p-nitrophenyl phosphate, followed by incubation at 30°C for 10 min, and terminated by the addition of 10 l of 13% (w/v) KH2PO4. The absorbance of the samples was measured immediately at 405 nM. The difference between the amounts of p-nitrophenol released in the absence and the presence of ciclosporin represented the phosphatase activity mediated by calcineurin. One unit of enzyme activity is defined as nmol of p-nitrophenol released from p-nitrophenyl phosphate.min-1.mg protein-1.
Gene Expression Methods
We have used the A. fumigatus oligonucleotide slides version 2 for microarray hybridizations (for details see http://pfgrc.jcvi.org/index.php/microarray/array_description/aspergillus_fumigatus/version2.html). The RNA samples extracted, as described above, were further purified with the RNA easy kit (Qiagen, Germany) and directly labelled by incorporation of Cy3- or Cy5-dUTP (GE Health Care). The resulting data was averaged from duplicate genes on each array, from dye-swap hybridizations for each experiment, and from two biological replicates, taking a total of 8 intensity data points for each gene. Differentially expressed genes at the 95% confidence level were determined using intensity-dependent Z-scores (with Z = 1.96) as implemented in MIDAS and the union of all genes identified at each time point were considered significant in this experiment. The resulting data were organized and visualized based on similar expression vectors in genes using Euclidean distance and hierarchical clustering with average linkage clustering method to view the whole data set and k-means to group the genes in 60 clusters with TIGR MEV (multi experiment viewer), also available at http://www.jcvi.org/cms/research/software. All the hybridization conditions and microarray data analysis were performed as previously described by Malavazi et al. . When RT-PCR was used to assess the reliability of the microarray hybridizations germlings were exposed to a novel growth curve (new RNA samples, not stocks of the original RNA used in the array experiment).
Real-time RT PCR reactions
All the PCR and RT-PCR reactions were performed using an ABI 7500 Fast Real-Time PCR System (Applied Biosystems, USA). Taq-Man™ Universal PCR Master Mix kit (Applied Biosystems, USA) was used for PCR reactions. The reactions and calculations were performed according to Semighini et al. . The primers and Lux™ fluorescent probes (Invitrogen, USA) used in this work are described in Additional file 4, Table S3.
Staining and microscopy
For cell imaging of RcnA fused to GFP, conidiospores were grown in glass-bottom dishes (Mattek Corporation, USA) in 2 ml of MM+2% glycerol for 24 hours at 30°C. All the confocal images were analysed using the Leica TCS SP5 laser scanning confocal microscope (Leica Microsystems, Heidelberg, Germany) (Laboratory of Confocal Microscopy, FMRP-USP, Brazil) using 63× magnification water immersion objective lens using laser lines 488 nm for GFP and 405 nm for DAPI. Images were captured by direct acquisition with the Leica LAS AF software (Leica Microsystems) and additional processing was carried out using Adobe Photoshop 7.0 (Adobe Systems Incorporated, CA).
DNA manipulations and construction of the Aspergilli conditional mutants
DNA manipulations were according to Sambrook and Russell . All PCR reactions were performed using Platinum Taq DNA Polimerase High Fidelity (Invitrogen). For the DNA-mediated transformation, the deletion cassettes were constructed by "in vivo" recombination in S. cerevisiae as previously described by Colot et al. . About 2.0-kb regions on either side of the ORFs were selected for primer design. For the construction of the A. fumigatus rcnA deletion, the primers calp-Afu P1 and calp-Afu P2 were used to amplify the 5'-UTR flanking region of the targeted ORF. The primers calp-Afu P3 and calp-Afu P4 were used to amplify the 3'-UTR ORF flanking region. For the construction of the A. nidulans rcnA deletion, the primers calp-Ani P1 and calp-Ani P2 were used to amplify the 5'-UTR flanking region of the targeted ORF. The primers calp-Ani P3 and calp-Ani P4 were used to amplify the 3'-UTR ORF flanking region. Both fragments 5- and 3-UTR were PCR-amplified from genomic DNA using as templates the A4 strain for A. nidulans and AFU293 for A. fumigatus cassettes. The pyrG used in the Aspergilli cassettes for generating both deletion strains was used as marker for auxotrophy and were amplified (by using primers pyrG Fw and pyrG Rw) from pCDA21 plasmid .
Cassettes generation was achieved by transforming each fragment for each construction along with the plasmid pRS426 BamHI/EcoRI cut in the in S. cerevisiae strain SC9421 by the lithium acetate method . The DNA of the yeast transformants was extracted by the method described by Goldman et al. , dialysed and transformed by electroporation in Escherichia coli strain DH10B to rescue the pRS426 plasmid harboring the cassettes. The cassettes were PCR-amplified from these plasmids and used for transformation of Aspergilli according to the procedure of Osmani et al. . Transformants were scored for their ability to grow on minimal medium. PCR or Southern blot analyses were used throughout of the manuscript to demonstrate that the transformation cassettes had integrated homologously at the targeted A. fumigatus or A. nidulans loci.
The A. fumigatus alcA::AfcrzA and A. nidulans alcA::AncrzA constructions were performed by amplifying by PCR 5'-end fragments (for A. fumigatus, 1084-bp from the start codon of the ORF with the primers Afcrz1 AscI: 5'-GGCGCGCCAATGGCTTCACAGGAGATGTTCC-3' and Afcrz1 PacI: 5'-CCTTAATTAAGCACATTGGGCATCATTTCCTGTCC-3'; and for A. nidulans, 1068 bp from the start codon of the ORF with the primers AncrzA AscI 5'-GGCGCGCCAATGGATCCTCAAGATACGCTGCAGG-3' and AncrzA PacI 5'-CCTTAATTAACATCTGTGACGCTTGCCCGATATC-3'), digesting them with Pac I and Asc I, and cloning them in the corresponing Pac I and Asc I restriction sites of the pMCB17-apx plasmid. The fragment of the ORF is under the control of the A. nidulans alcA promoter and after homologous integration the translation produces an N-terminal fusion protein. A. fumigatus and A. nidulans pyrG - strains were transformed with the corresponding vectors pMCB17-apx-crzA and after homologous recombination the alcA::gfp::crzA construction and a truncated crzA non-coding gene were generated. All the transformants were confirmed by PCR using specific primers.
We would like to thank the Laboratories of Confocal Microscopy and Electronic Microscopy from the Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Brazil, for the use of the confocal microscope, and the four anonymous reviewers for their suggestions. This research was supported by the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil, and John Simon Guggenheim Memorial Foundation, USA.
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