Functional characterisation of the non-essential protein kinases and phosphatases regulating Aspergillus nidulans hydrolytic enzyme production
© Brown et al.; licensee BioMed Central Ltd. 2013
Received: 27 March 2013
Accepted: 18 June 2013
Published: 25 June 2013
Despite recent advances in the understanding of lignocellulolytic enzyme regulation, less is known about how different carbon sources are sensed and the signaling cascades that result in the adaptation of cellular metabolism and hydrolase secretion. Therefore, the role played by non-essential protein kinases (NPK) and phosphatases (NPP) in the sensing of carbon and/or energetic status was investigated in the model filamentous fungus Aspergillus nidulans.
Eleven NPKs and seven NPPs were identified as being involved in cellulase, and in some cases also hemicellulase, production in A. nidulans. The regulation of CreA-mediated carbon catabolite repression (CCR) in the parental strain was determined by fluorescence microscopy, utilising a CreA::GFP fusion protein. The sensing of phosphorylated glucose, via the RAS signalling pathway induced CreA repression, while carbon starvation resulted in derepression. Growth on cellulose represented carbon starvation and derepressing conditions. The involvement of the identified NPKs in the regulation of cellulose-induced responses and CreA derepression was assessed by genome-wide transcriptomics (GEO accession 47810). CreA::GFP localisation and the restoration of endocellulase activity via the introduction of the ∆creA mutation, was assessed in the NPK-deficient backgrounds. The absence of either the schA or snfA kinase dramatically reduced cellulose-induced transcriptional responses, including the expression of hydrolytic enzymes and transporters. The mechanism by which these two NPKs controlled gene transcription was identified, as the NPK-deficient mutants were not able to unlock CreA-mediated carbon catabolite repression under derepressing conditions, such as carbon starvation or growth on cellulose.
Collectively, this study identified multiple kinases and phosphatases involved in the sensing of carbon and/or energetic status, while demonstrating the overlapping, synergistic roles of schA and snfA in the regulation of CreA derepression and hydrolytic enzyme production in A. nidulans. The importance of a carbon starvation-induced signal for CreA derepression, permitting transcriptional activator binding, appeared paramount for hydrolase secretion.
KeywordsCarbon catabolite repression Cellulase Xylanase SchA SnfA
Lignocellulolytic fungi secrete a complex arsenal of enzymes that synergistically deconstruct plant cell wall polysaccharides. The capacity of these enzyme cocktails to release utilisable sugars from non-food lignocellulosic material represents an opportunity for the development of a new generation of biofuels, produced directly from plant biomass without the use of extensive pre-treatment. However, efficiencies in industrial enzyme production require dramatic improvement, as the presence of readily metabolisable carbohydrates strongly impedes cellulase and hemicellulase production via carbon catabolite repression (CCR) [1, 2]. Genome-wide studies have provided insights into how fungi alter transcription, metabolism and enzyme secretion in response to carbohydrate availability [3–6]. An enhanced understanding of CCR in lignocellulolytic fungi is required for the engineering and exploitation of such regulatory networks to increase enzyme secretion, reducing the costs involved in enzyme production and increasing fermentation efficiency.
In fungi, lignocellulolytic enzyme production is tightly controlled at the transcriptional level by the competitive action of transcriptional activators and repressors . In Aspergillus nidulans, Hypocrea jecorina and Neurospora crassa the orthologous repressors CreA/Cre1 have been shown to block the transcription of genes associated with the utilisation of alternate carbon sources when glucose is present, including cellulolytic and xylanolytic enzymes [8–10]. The A. nidulans CreA protein has two Cys2His2 zinc finger DNA binding structures that demonstrate high similarity to the zinc fingers of the Mig1 repressor involved in Saccharomyces cerevisiae CCR  and has been demonstrated to be regulated at both the transcriptional and post-translational level .
The transcription of genes involved in alternative carbon utilisation also requires the action of transcriptional inducers. In Aspergilli the ethanol utilisation pathway is tightly controlled by CreA-mediated CCR and positively induced by the regulon specific transcription factor AlcR. The positive regulator, AlcR, has overlapping binding sites with CreA, suggesting a competitive binding mode of action, while nucleosomal positioning and chromatin organisation has been shown to play a role . Other alternative carbon source genes adopt a similar mechanism of competitive induction including the conserved transcription factors AraR and XlnR, which positively control hemicellulase expression . Interestingly, in H. jecorina the cellulase activator, Ace2, has been shown to bind to the same promoter motif as XlnR, while the Hap2/3 complex opens the chromatin structure, promoting nucleosome reassembly and derepression . In N. crassa and A. nidulans, two newly identified transcription factors, ClrA and ClrB, have been shown to be required for cellulase activity and expression .
Sensing the external environment and intracellular energetic status ensures that a fungal organism can balance the requirements for growth and cell survival. S. cerevisiae has served as a model organism for the study of such cellular responses. However, many differences are known to exist in filamentous fungi, due to the adoption of different life styles. Protein phosphorylation state represents the most common form of post-translational modification. Protein kinases and phosphatases perform a central role in the transduction of such signals via modulating protein phosphorylation state and activity, thus coordinating subsequent responses. The importance of protein kinases and phosphatases is demonstrated by the fact that 30% of the S. cerevisiae genome is modified by these proteins, while collectively kinase and phosphatase genes represent only 6% of the genome .
The most well studied examples included the mitogen-activated protein kinases (MAPK), which form the pheromone response, filamentous growth, the osmotic stress response and cell wall integrity pathways. The sensing of glucose or pheromones by the G-protein coupled receptors (GPCRs), results in the activation of the cAMP-protein kinase A (PKA) pathway and the MAPKs cascade, which influence filamentous growth . Intracellularly, glucose is phosphorylated by hexo- and/or gluco-kinases activating Ras2 signalling that also induces the filamentous growth cAMP-PKA and MAPK pathways . Apart from the well-studied roles in growth, fungal homologues of the S. cerevisiae pheromone response/filamentous growth MAPKs have been shown to influence the secretion of hydrolytic enzymes in various plant pathogenic fungi including; Alternaria brassicicola, Cochliobolus heterostrophus and Fusarium oxysporum[20–22].
Homologues of the S. cerevisiae sensors of cellular energetic state Snf1 (sucrose non fermenting) and TOR (target of rapamycin) have been widely identified in filamentous fungi [23–28]. The Snf1 has been demonstrated to be required for growth on alternative carbon sources and also regulates the expression of 400 genes in response to carbon exhaustion . The absence of the Snf1 homologue in filamentous fungi, including Cochliobolus carbonum, Ustilago maydis and F. oxysporum, has been shown to reduce hydrolytic enzyme production [24–26]. The essential TOR kinase complexes control cell growth and metabolism in response to environmental cues . TOR has traditionally been related to nitrogen utilisation. However, TOR signalling also influences the expression of AreA-controlled genes involved in carbon metabolism . Therefore TOR may perform dual roles in integrating both carbon and nitrogen signals. Different to the aforementioned kinases, the A. nidulans genome contains fewer phosphatases (http://www.aspgd.org), suggesting that each phosphatase demonstrates less specificity and dephosphorylates multiple kinase targets. The known kinase/phosphatase signalling pathways have been proven to be highly conserved and closely interlinked, either regulating one another or the same gene sets, enabling the fine tuning of cellular responses to the extra- and intracellular environment.
Despite recent advances in the understanding of hydrolytic enzyme regulation, less is known about how different carbon sources are sensed and which signalling cascades are subsequently activated, thus coordinating the adaptation of cellular metabolism and hydrolase secretion to the respective carbon source [16, 31, 32]. Subsequently, this study identified 11 non-essential protein kinases (NPKs) and seven phosphatases (NPPs) involved in cellulase and in some cases also hemicellulase production in A. nidulans. The involvement of the identified NPKs in starvation/cellulose-induced responses and CreA derepression was assessed by transcriptomics and fluorescence microscopy of the CreA::GFP in the parental and NPK mutant backgrounds. Collectively, this study demonstrated the overlapping, synergistic roles of the NPKs schA and snfA in the regulation of CreA derepression and hydrolytic enzyme production. In addition, a period of carbon starvation appeared paramount for CreA derepression and hydrolase induction.
Screening the NPKs collection for involvement in cellulase production
The eleven NPKs that demonstrated reduced growth on AVICEL show a conserved theme in nutrient sensing and cell growth
A. nidulans gene name
Yeast best hit
Phospholipid metabolism, DNA damage, cell polarity, starvation
RAM signalling, regulates cell morphogenesis
Regulates endocytosis, sphingolipid synthesis
MAP kinase, germination, polarised growth
Promotes growth in response to nutrition
Negative regulation of pyruvate dehydrogenase
Actin filament organisation, endocytosis
Upstream activator of SNF1 complex
cAMP signalling, role overlaps with Ras/PKA, regulated by TOR complex
Required for transcription of glucose repressed genes
Inhibits growth in response to glucose, negatively regulated by Ras/PKA
Screening of the non-essential phosphatase (NPP) collection for involvement in cellulase production
The functional description of the seven NPPs that demonstrated reduced growth on AVICEL and reduced eglA/B transcription
A. nidulans gene name
Yeast best hit
Oxidative stress resistance
Cell cycle, mitotic exit, meiotic progression
Type 2C protein phosphatase, inactivates osmotic stress and activates pheromone response MAPK pathways
Inactivates osmotic stress MAPK pathway
Type 2A-like phosphatase, required for glycogen accumulation, associates with Tap42
G1/S transition of the mitotic cycle, modulates functions mediated by Pkc1p including cell wall and actin cytoskeleton organization
Protein kinase A (PKA) activity is hyperactivated upon carbon starvation and growth on AVICEL
Extracellular glucose is detected via extracellular GCPRs, while intracellular phosphorylated glucose results in RAS activation, with both routes accumulating with adenylate cyclase synthesising cAMP and PKA activation. To confirm that the conventional route of cAMP dependent PKA activation inhibited cellulase production during growth on cellulose, the endocellulase activity of constitutively activated RASG17V strain  was assessed, as this would result in a constant positive signal for repression. The RASG17V strain demonstrated an approximate eight-fold reduction in endocellulase activity after 5 days growth in MM plus AVICEL (parental, 484 ± 48 U/ml; RASG17V, 60 ± 6 U/ml). This confirmed that the conventional route of PKA activation inhibits cellulase production, while suggesting that starvation induced PKA hyperactivation performed alternative function(s) that directly or indirectly contributed to growth on cellulose.
Evaluation of CreA nuclear localisation
In order to monitor the dynamics of CCR in A. nidulans a CreA::GFP tagged protein under the control of the native promoter was constructed, enabling the study of CreA nuclear localisation under repression/derepression and the evaluation of the signalling components that led to CreA cellular compartmentalisation. The CreA::GFP strain constructed in the present work, demonstrated growth similar to the parental strain on various repressing and derepressing carbon sources (Additional file 1: Figure S1). The microscopic analysis of fluorescence in different carbon sources, including various simple and complex polysaccharides, non-polysaccharides and carbon starvation, assisted in the understanding of the signals involved in CreA nuclear localisation and repression.
CreA::GFP nuclear localisation post transfer between media containing different carbon sources
Glucose 16 h (82)
Xylose 2 h (48)
Cellobiose 2 h (74)
Xylan 5 h (114)
AVICEL 5 h (74)
Glycerol 2 h (32)
No carbon 5 h (35)
Xylose 16 h (24)
Glucose 1 h (20)
AVICEL 16 h (22)
Glucose 1 h (30)
Glucose 16 h followed by no carbon 5 h (50)
Glucose 1 h (32)
2-deoxyglucose 1 h (44)
6-deoxyglucose 1 h (35)
Glucose 16 h (24)
AVICEL 5 h (31)
Glucose 16 h (19)
AVICEL 5 h (28)
Glucose 16 h (20)
Avicel 5 h (22)
Glucose 16 h (20)
Avicel 5 h (20)
Growing the CreA::GFP strain overnight in glucose (100% nuclear localisation) and then exposing it to carbon starvation for 5 h (~0% nuclear localisation) enabled the study of the positive signals for CreA repression. The addition of 2-deoxyglucose which cannot be successfully metabolised, or 6-deoxyglucose that cannot be phosphorylated, to the carbon starved cultures demonstrated that the positive signal for CreA nuclear localisation required glucose phosphorylation (Table 3).
Confirmation of NPK involvement in CCR
Sexual crosses between several of the NPK mutants identified from the screening of the kinase collection with either the ∆creA4 strain  or the CreA::GFP strain enabled the confirmation that schA and snfA were required for CreA derepression and endocellulase production. The absence of schA and snfA resulted in an inability to remove CreA from the nucleus upon growth on AVICEL (Table 3). Similarly, sexual crosses between ∆schA or ∆snfA with the ∆creA4 strain restored the endocellulase activity of these NPKs to parental levels (Additional file 2: Figure S2). However, the absence of atmA or the atmA- regulated transcription factor xprG did not affect CreA nuclear localisation or derepression (Table 3). Collectively, these datasets suggest that schA and snfA are required for CreA derepression thus permitting cellulase gene induction upon growth on AVICEL, while atmA performed additional functions that contributed to cellulase production.
Microarray analysis revealed the roles performed by schA and snfA during growth on AVICEL
The overrepresented GO terms from the FetGOat analysis ( p <0.05) of the genes differentially expressed within the parental and ∆ schA strains post transfer from CM to MM plus AVICEL for 24 h
Carbohydrate catabolism / metabolism
Carbohydrate catabolism / metabolism
Ribosome biogenesis and rRNA processing
Respiration and energy production
maturation of SSU-rRNA
maturation of SSU-rRNA
energy derivation by oxidation of organic compounds
generation of precursor metabolites and energy
quinone cofactor metabolism
ribosomal subunit biogenesis
quinone cofactor biosynthesis
The modulation of genes involved in transport was assessed. Different groups of transporters were either up regulated upon 24 h growth on AVICEL in all strains (14 transporters), in both the parental and the ∆schA strains (33 transporters), in both the parental and ∆snfA strains (6 transporters), or specifically in the parental strain (41 transporters). Note the low number of transporters induced in the ∆snfA strain. The far majority of the transporters induced in the parental strain lacked a defined function in A. nidulans. However, the functionally defined genes included transporters of amino acid, sugar, iron, calcium and sodium (Additional file 5: Table S3). The putative sugar (AN6669) and the alpha glucoside (AN3204) transporters were only up regulated in the parental strain, while an additional putative sugar transporter (AN8737) and a high affinity hexose transporter (AN6923) were induced in both the parental and ∆schA strains.
In all strains there was an induction of the xprG starvation response transcription factor and hacA, which regulates the unfolded protein response, after 24 h growth on AVICEL, suggesting the existence of starvation induced stress. Accordingly, several starvation-related genes, atg8, hxkC and the GPCR gprH were also up regulated. However, despite the induction of xprG in all strains these three starvation-response genes were not induced in the ∆snfA strain, while the xprG- activator kinase gene atmA (Krohn N, unpublished results), was repressed at a low level. Other kinase sensors of energetic status including the sakA and the gal83 homolog, which are both required for Snf1 activation and nuclear localisation in S. cerevisiae, were only induced in the parental strain, while the TOR kinase (AN5982) was only not induced in the ∆schA strain.
Collectively, the transcriptomic data depicts how schA and snfA are required to regulate the response to carbon limitation and growth on AVICEL. These two NPKs demonstrated a partially overlapping function in the modulation of CAZy enzyme, sugar and amino acid transporters, transcription factors and metabolism, with snfA appearing to be of paramount importance.
The transcription of lignocellulolytic enzymes is tightly controlled by the competitive action of the CreA repressor and polysaccharide specific inducers. This study demonstrated that carbon starvation resulted in the loss of CreA from the nucleus and derepression, similar to the Mig1 mechanism observed in S. cerevisiae. A previous investigation of CreA cellular localisation utilised a fusion protein under the control of a constitutive promoter and implied that intracellular localisation was not involved in the regulation of CreA-mediated repression . Such an approach could overwhelm the system and may have contributed to the differences observed between the two experimental designs. Again similar to S. cerevisiae, the absence of the A. nidulans Snf1 homolog, which in S. cerevisiae is involved in Mig1 nuclear export and alternative carbon usage , resulted in a reduced ability of A. nidulans to utilise cellulose, transcribe hydrolytic enzymes and relocalise CreA. This appears to be in contrast to H. jecorina where the Snf1 homologue has been shown to phosphorylate Mig1 when expressed in S. cerevisiae but not the H. jecorina counterpart , while Cre1 phosphorylation in H. jecorina has been shown to positively regulate DNA binding . The similarity between CreA depression during growth on cellulose and carbon starvation, suggested that A. nidulans was experiencing starvation under both conditions. The induction of cellulases and hemicellulases when grown on cellulose as a sole carbon source, which would therefore lack a pentose metabolites and a hemicellulase inducer, has also previously been reported under carbon starvation  and could be the consequence of CreA derepression rather than polysaccharide specific induction. This is supported by the observation that CreA nuclear localisation was high in the presence of cellobiose, a known inducer of cellulases . This concept suggests that a transient period of starvation is required from CreA derepression, thus liberating the inducer binding sites for gene induction. This is fitting with the model proposed by Delma and colleagues which observed the induction of a subset of hydrolytic enzymes under starvation conditions that were suggested to perform a scouting role .
In S. cerevisiae, the external sensing of glucose via the GPCRs-PKA pathway and the intracellular phosphorylation of glucose, which results in RAS activation, promotes Mig1-mediated CCR . However, in A. nidulans the presence of extracellular glucose proved not to be essential, while glucose phosphorylation was essential, for CreA repression. As shown by the inability to recover CreA nuclear localisation after the addition of the non phosphorylatable 6-deoxyglucose to carbon starved CreA derepressed cultures, while CreA repression was recovered by the addition of the non metabolisable 2-deoxyglucose. The reduced endocellulolytic capacity of the activated RASG17V strain when grown on cellulose supported the concept that glucose phosphorylation and RAS signalling induces CreA repression. Interestingly, pkaC was identified as being required for growth similar to that of the parental strain on cellulose, while PKA activity was hyperactivated during growth on cellulose and carbon starvation. This suggests that the PKA performs additional starvation-induced roles, apart from CreA repression, which in A. nidulans that may directly, or indirectly, influence growth and survival on cellulose. During starvation, PKA activity increases in mammalian cells, promoting mitochondrial elongation, preventing autophagic degradation and maintaining ATP production, while the blocking of mitochondrial elongation precipitates in starvation-induced death . In H. jecorina, a complex mechanism of light-dependent cellulase regulation has been shown to involve the adenylate cyclase (Acy1) and Pkac1. Schuster et al. demonstrated that Acy1 had a positive effect on cellulase gene expression in light and darkness, while Pkac1 only positively influenced cellulase expression in light, but negatively influenced in darkness. Thus in A. nidulans PKA may perform additional functions during starvation and growth on cellulose, apart from the typical GPCR/Ras-PKA pathways (Figure 9).
Several additional NPKs involved in the starvation response of multiple organisms, such as the atmA and pkpA were also identified as being required for growth on cellulose and endocellulolytic enzyme production. In mammalian cells, the pyruvate dehydrogenase complex (PDC), generates NADPH and acetyl CoA from the oxidative decarboxylation of pyruvate and facilitates uptake into the mitochondria. The phosphorylation state of the PDC controls the flux through this irreversible reaction, thus directing metabolism towards the consumption of glucose in respiration or the preservation of glucose for gluconeogenesis . Under starvation the pyruvate dehydrogenase kinase phosphorylates and inactivates the PDC conserving glucose and promoting fatty acid utilisation . Therefore, the identification of the pkpA kinase suggests that a period of glucose deprivation is experienced by A. nidulans when grown on cellulose, which is supported by the observed up regulation of alternative carbon source usage, such as amino acid, ethanol, acetate, fatty acid and cellulose.
The ATM kinase in mammalian cells has been identified as being involved in starvation, insulin signalling and the regulation of glucose homeostasis through the action of the p53 phosphorylation target, which in turn regulates metabolism, mitochondrial respiration and glucose transporters. In addition, a p53-independent ATM pathway has been demonstrated to activate AMPK (the mammalian SnfA homolog) via LKB1 (the mammalian homolog of SakA) via dependent and independent routes [43–45]. Low glycolytic rates and energy stress experienced by A. nidulans grown on cellulose could result in a similar AtmA, SakA and SnfA cascade of activation, thus regulating mitochondrial function, sugar uptake, fatty acid utilisation and hydrolytic enzyme production.
The presented study demonstrated how SnfA performed a key role in CreA derepression and the modulation of transcription, metabolism and hydrolytic enzyme secretion. In mammalian and S. cerevisiae cells the SnfA homologs have been shown to interact with the essential TOR kinase, which is an integrator of nutrient and growth factor inputs that control cell growth . Interestingly, homologs of two phosphatases revealed in this study to be required for hydrolytic enzyme production and growth on cellulose, are involved in TOR signalling in S. cerevisiae. Homologs of the SchA kinases have been shown to operate downstream of TOR . The overlapping but lesser role of the SchA kinase, when compared to SnfA, in the regulation of the transcriptional response to growth on cellulose, in addition to the similar inability to relocalise CreA upon growth on cellulose, suggests that SchA may also have synergistic functions to SnfA in A. nidulans, possibly integrating the TOR signal. Similarly in S. cerevisiae and A. nidulans, the SchA kinase has also been shown to have synergistic and opposing functions with PKA, in the regulation of transcription [33, 47].
Multiple NPKs and NPPs involved in filamentous growth, polarisation, and morphogenesis were also identified as being required for growth on cellulose and hydrolase secretion. Endo- and exo-cytosis are key processes for the sensing of, and interaction with, the environment. Such processes have been shown to regulate glucose transporters in mammalian cell . Therefore, the identification of such NPKs and NPPs could represent the impact of these mutations on endo- exo-cytosis, thus influencing secretion, the distribution of transporters in the cell membrane and the import of inducer molecules.
An initial period of carbon starvation appears to play a role in the activation of the nutrient/energy sensing kinase pathways and that CreA derepression is an essential prerequisite for hydrolytic enzyme induction. Through homology with more extensively studied systems, a model for how the identified kinases and phosphatases regulate hydrolytic enzyme production can be postulated. However, the genetic interactions between these kinases and phosphatases in A. nidulans require further study prior to the reconstruction of relevant signalling cascades. Even so, it is clear that SnfA-mediated CreA derepression and transcriptional responses, which regulate metabolism, transport and hydrolytic enzyme secretion, are paramount for growth on cellulose, while the SchA kinase appeared to have an overlapping mechanism and synergistic function with SnfA.
Strains and culture conditions
The parental A. nidulans TNO2a3 (pyrG89; pyroA4; nkuA::argB) strain was used as a reference in all experiments. The null mutant collections of 103 non-essential protein kinases (NPKs) and 28 non-essential phosphotases, created by in vivo recombination in S. cerevisiae followed by A. nidulans protoplast transformation (http://www.fgsc.net/Aspergillus/KO_Cassettes.htm; [49, 50]) were utilised. The ∆cyaA and the activated RASG17V strains were provided by N. Keller, University of Wisconsin-Madison, USA . The ∆CreA strain was provided by M. Flipphi, Instituto de Agroquímica y Tecnología de Alimentos, Spain . All fungal strains were propagated on complete (2% w/v glucose, 0.5% w/v yeast extract, trace elements) or minimal media (1% w/v glucose, nitrate salts, trace elements, pH 6.5) plus 2% w/v agar.
Screening for reduced growth on AVICEL
Complete media (CM) cultures (50 ml) were inoculated with 1×107 conidia and incubated on a rotary shaker (180 rpm) set at 37°C for 24 h. Liquid minimal media (MM) cultures containing 1% AVICEL, instead of glucose as a carbon source were prepared as with the CM cultures, but were incubated for 10 days under the same conditions. The mycelia of the CM and MM plus AVICEL cultures were filtered, frozen in liquid nitrogen and freeze dried prior to the determination of dry weight and total protein content, respectively. The fungal biomass (dry weight) within the MM plus AVICEL cultures cannot be measured directly, due to the presence of AVICEL. Therefore, total protein content was used as a relative measurement. The mycelia from the AVICEL cultures was ground in liquid nitrogen and added immediately to the protein extraction buffer (Tris base pH 7.5 25 mM, EGTA pH 7.5 15 mM, MnCl2 15 mM, plus a protease inhibitor cocktail (Roche)), vortexed for 5 min prior to centrifugation for 15 min at 14000 g. Protein content was measured using the Bio-Rad protein assay according to manufacturer’s instructions.
Media shift experiments and enzyme activity assays
Cultures of MM plus 1% fructose (50 ml) were inoculated with 1×107 conidia and incubated on a rotary shaker (180 rpm) set at 37°C for 24 h. Subsequently, the mycelia of the transfer cultures were washed with sterile water, resuspended in liquid MM plus 1% AVICEL or xylan and incubated under the same conditions for 5 or 3 days depending on the respective carbon source. The cultures were filtered and the mycelia frozen in liquid nitrogen prior to being freeze dried for RNA extraction. The culture supernatants were collected for endo- cellulase or xylanase activity assays (Megazyme) according to manufacturer’s instructions.
Peptag cAMP dependant protein kinase A (PKA) activity assays
Media shift cultures were prepared as described previously. Post washing, the mycelia was transferred to a range of different carbon sources, as stated in the relevant figure and results section, for 8 h. The mycelia from the transfer cultures was collected by filtration, then frozen and ground in liquid nitrogen. Total protein was extracted as described previously and the Peptag cAMP dependent PKA activity assay (Promega) performed according to manufacturer’s instructions. Quantification of the intensity of the phosphorylated substrate was determined via densitometry analysis using the ImageJ software. Results are presented as the total PKA activity per culture.
Construction of modified strains
The construction of the CreA::GFP strain was performed according to Colot et al. . Standard molecular techniques were performed according to Sambrook and Russel . The 5’ untranscribed region (UTR) plus the creA gene (minus the stop codon), the gfp gene plus a spacer, the pyrG gene and the 3’ UTR were co-transformed into S. cerevisiae. Homologous recombination within S. cerevisiae created the construct, which was subsequently amplified from pooled S. cerevisiae DNA, and 20 μg transformed into TNO2a3 according to Osmani et al., . Transformants were selected via their ability to grow on solid MM plus pyridoxine in the absence of uridine and uracil. Homologous integration was confirmed via PCR. Sexual crosses between the CreA::GFP or ∆CreA strains with the ∆schA and ∆snfA strains were confirmed by PCR, using the relevant external forward and exon reverse primers, while the absence of atmA was confirmed via increased camptothecin sensitivity (75 μM). The primers used are listed in Additional file 6: Table S4.
Strains were inoculated onto a coverslip and incubated for 12 h at 25°C in liquid MM plus various carbon sources (1% carbon w/v). During media shift experiments the coverslips were washed with MM lacking a carbon source prior to the addition of the following media and incubated at 25°C, for the duration stated in the text (dependent on carbon source). In the case of 2-deoxyglucose and 6-deoxyglucose, a final concentration 6 mM of either compound was added to 5 h carbon starved cultures and incubated for an additional hour prior to examination. Mycelia mounted on the coverslips were washed with phosphate buffered saline (PBS; 140 mM NaCl, 2 mM KCl, 10 mM NaHPO4, 1.8 mM KH2PO4, pH 7.4). The mycelia were then stained with 100 ng/ml Hoescht 33258 (Molecular Probes) for 2 min. The mycelia were washed again in PBS and examined using a Zeiss epifluorescence microscope with excitations of 359, 498 nm and emissions 461, 516 nm for Hoescht and GFP respectively. Phase contrast bright-field and fluorescent images were captured with AxioCam camera (Carl Zeiss) and processed using the AxioVision software version 3.1.
RNA extraction and quantitative PCR
Total RNA was isolated using TRIZOL (Invitrogen), treated with DNase (Promega) and purified using the RNeasy® Mini Kit (Qiagen) according to manufacturer’s instructions. RNA integrity was confirmed using the Bioanalyser Nano kit (Agilent technologies) and the Agilent Bioanalyser 2100. Purified RNA was used for cDNA synthesis using Superscript III (Invitrogen) according to manufactures instructions. Quantitative PCRs were performed as previously described . The Taqman fluorescent probes (Invitrogen) used for the endoglucanase genes eglA (AN1285) and eglB (AN3418)  are listed in Additional file 6: Table S4. Expression of the tubulin gene tubC (AN6838) was used as an endogenous control.
The parental, ∆schA and ∆snfA strains (1×107 conidia) were incubated in 50 ml CM on a rotary shaker (180 rpm) set at 37°C for 24 h. The mycelia were washed with sterile water and transferred to MM plus AVICEL for 8 and 24 h. Post incubation, the mycelia was collected by filtration and frozen in liquid nitrogen. Total RNA was extracted and integrity confirmed as described previously. The synthesis of cDNA from 200 ng of RNA and the array hybridisations were performed according to Souza et al. with a minor modification to the quantity of RNA used. The RNA isolated from the CM cultures was used as the reference for the MM plus AVICEL of each strain. The dataset was deposited in the Gene Expression Omnibus (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE47810).
Genes were determined as differentially expressed between the CM and MM plus AVICEL via a t-test (p < 0.01) performed within the Mev software . The overrepresented GO terms within the differentially expressed gene sets from each strain were identified using the FetGOat software (http://www.broadinstitute.org/fetgoat/index.html). The differential regulation of gene expression between the three strains post transfer to MM plus AVICEL was determined via venn analysis and the functional profile of the gene lists determined using FunCats (http://www.pedant.gsf.de/pedant3htmlview/pedant3view?Method=analysisDb=p3_p130_Asp_nidul). Secreted proteins and hydrolytic enzymes were identified using TargetP (http://www.cbs.dtu.dk/services/TargetP/) and the CAZy enzyme database (http://www.cazy.org/) respectively.
Three biological replicates were performed for all experiments and the statistical tests for significance determined via a one-tailed t-test (* P <0.05, ** P < 0.01, *** P < 0.001), unless stated otherwise, using Prism 3.0 (GraphPad).
NAB contributed to the concept, design, acquisition and analysis of data, in addition to the preparation of the manuscript. PG, NK and MS contributed to the acquisition of data, and GHG contributed to the concept and design of the investigation in addition to the preparation of the manuscript. All authors have read and approved the final manuscript.
Cyclic adenosine monophosphate
Carbohydrate active enzymes
Carbon catabolite repression
Green fluorescent protein
G-protein coupled receptor
Mitogen activated protein kinase
Nicotinamide adenine dinucleotide phosphate
Non-essential protein kinase
Non-essential protein phosphatase
Protein kinase A complex
Pyruvate dehydrogenase complex
We would like to thank the Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil, for providing financial support. We also thank Dr. Nancy Keller, University of Wisconsin-Madison, USA for providing the A. nidulans ∆cyaA and activated RASG17V mutant strains, Dr. M. Flipphi, Instituto de Agroquímica y Tecnología de Alimentos, Spain, for the ∆CreA4 strain, Dr. Steve A. Osmani for providing the non-essential phosphatase (NPP) collection, and the two anonymous reviewers for their comments and suggestions. We also acknowledge the Program Project grant GM068087 (PI Jay Dunlap) for providing the non-essential kinase (NPK) collection.
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