Background

Bioconversion of the abundant renewable plant biomass consisting of lignocellulose holds great potential for the production of environmental friendly energy and chemicals [1]. Lignocellulose is primarily made of various interconnected biopolymers (e.g., cellulose, hemicellulose and lignin) and displays significant structural heterogeneity and complexity, which render them recalcitrant to degradation [2]. The industrial use of plant biomass involves mechanical, chemical or physicochemical pretreatment steps followed by enzymatic hydrolysis to release the constituent monosaccharides for further fermentation to produce biofuels and biochemicals [3, 4]. As for the enzymatic hydrolysis step, multiple lignocellulosic enzymes, including cellulases, hemicellulases and polysaccharide lyases, are required to act synergistically to depolymerize cellulose and hemicellulose [5,6,7]. Preparation and use of these enzymes are therefore a major cost factor either due to the low catalytic performance and/or to the suboptimal composition of the enzyme cocktail under industrial conditions [8, 9].

The large amounts of lignocellulosic enzymes (e.g., cellulases and hemicellulases) secreted by the ascomycete Trichoderma reesei represent the prominent source of enzyme cocktails that are used in industry for biomass degradation [10,11,12]. Although industrial T. reesei strains have been reported to produce cellulases over 100 g/L [13], the cost of enzyme production used in the saccharification step is still considered to be the major bottleneck of biomass conversion for the economical production of biofuels and biochemicals. Not surprisingly, T. reesei has been the subject of intensive investigation toward the improvement of its cellulases including increasing or reinforcing their existing activity and production to reduce the costs for biofuel production. The production of lignocellulosic enzymes by T. reesei involves many physiological processes including extracellular signal sensing [14, 15], intracellular signal transduction [16], transcriptional regulation of cellulase genes and protein synthesis [17, 18], and secretion [19]. Understanding the molecular mechanism behind these processes is crucial to further improve cellulase productivity of T. reesei.

Although the genomic sequence of T. reesei is now available, genes without an explicit function make up a large portion of the genome due to limited and intricate genetic manipulation approaches [20]. The gene knockout strategy by homologous recombination (HR) has been developed and widely used in T. reesei to study the function of particular genes [21, 22]. However, HR in T. reesei usually involves labor-intensive plasmid constructions for incorporating sufficiently long homologous arms on both sides of the target gene to ensure its occurrence at an inherent low efficiency [23]. As a result, large amounts of screening efforts are then needed to obtain the appropriate knockout strain. Although the low efficiency of HR has been partially solved by inactivating the genes (e.g., tku70) in non-homologous end joining (NHEJ) pathway [23, 24], deleting these important DNA repair genes may exert unanticipated side effects. To solve this issue, Chum et al. [25] recently improved the efficiency of HR to certain extent by only transiently silencing tmus53 gene of NHEJ pathway. Nevertheless, the gene knockout strategy is improper to study a large proportion of important or essential genes, whose deletion proves to be intractable and results in severe growth defect or even inviability, making the phenotypic characterization impossible. On the other hand, tunable promoters controlled by external conditions have been shown to be useful for investigating the function of target genes in T. reesei [26, 27]. Developing effective genetic manipulation systems by combining these induced or repressible promoters with conventional gene-targeting strategies is thus of prior importance to fully characterize such essential genes and genes with unknown functions.

The post-transcriptional gene silencing by small interfering RNA (siRNA)-mediated RNAi is triggered by double-stranded RNA and exists extensively in eukaryotes [28]. Soon after its discovery, RNAi becomes a powerful tool for functional genomic study due to its targeted nature, silencing of genes to the equivalent of null mutants and applicability to any transformable species of lower or higher eukaryotes [29, 30]. In many cases, RNAi is initiated by expressing a target gene fragment cloned as a tandem inverted repeat separated by a hairpin-forming intron sequence [29, 31]. The transcript creates a hairpin RNA (hpRNA) that then serves as a template for the RNAi machinery. There have been several studies describing the modulation of transcript abundance of specific genes in T. reesei using RNAi [31, 32]. Specifically, Qin et al. [31] have reported an inducible RNAi system with the cel7a promoter allowing induction of hpRNA expression in response to cellulose. Schmoll et al. [32] reported the knocking down of gan3, an adenylate cyclase-activating class III of G-alpha subunit, by expressing its antisense RNA driven by constitutive gpd1 promoter in T. reesei. These systems, however, were either uncontrolled or relied on the transition of nutritional state which may result in many other side effects complicating the explanation for the observed phenotypes.

Here, we present a copper-controlled RNAi-mediated knockdown system in T. reesei by combining the previously identified copper-responsive P tcu1 promoter with the routine RNAi vector for reversible silencing of different target genes. The usefulness of this system was demonstrated by the successful down-regulation of target genes in response to the absence of exogenous copper ions while maintaining their normal expression in the presence of copper. This copper-controlled RNAi system provides an alternative approach to characterize the functions of genes in T. reesei, especially those genes whose expression is under stringent regulation and thus extremely sensitive to any fluctuation in its expression level.

Methods

Strains and culture conditions

Escherichia coli DH5α was used for plasmid construction and cultured in lysogeny broth with a rotary shaker (200 rpm) at 37 °C. QM9414 (ATCC 26921) and a uridine auxotroph of T. reesei TU-6 (ATCC MYA-256) were used in this work as parental strains. The pyr4 gene-deleted strain of QM9414 (QM9414–∆pyr4) was used as a control strain for pyr4 gene knocking down. All T. reesei strains were maintained on malt extract agar or liquid media supplemented with 10 mM uridine when necessary. For the transcription and cellulase production analysis, spores were pre-grown in 1-L Erlenmeyer flasks on a rotary shaker (200 rpm) at 30 °C with 250 mL Mandels–Andreotti (MA) media containing 1% (v/v) glycerol as the carbon source for 48 h as previously described [18]. Mycelia were harvested by filtration and washed twice with media without a carbon source. Equal amounts of mycelia were then transferred to fresh media without peptone containing 1% (w/v) Avicel and incubation was continued for the indicated time periods. Copper was present or absent perpetually in the media from pre-culture to induction. For vegetative growth on agar plates, equal amounts of growing mycelia or spores were inoculated on minimal media agar plates containing 1% (w/v) glucose at 30 °C for several days. The Avicel double-layer plates where the minimal media agar without carbon source was covered by 1% (w/v) Avicel were used for investigating cellulase production.

Construction of plasmids and strains

The 744-bp HindIII–EcoRV fragment containing P tcu1 promoter, 1041-bp Spe1–Sal1 fragment containing T cel6a terminator and 179-bp EcoRV–Spe1 fragment containing I cel5a intron were amplified by PCR from the genomic DNA of T. reesei QM9414 and then inserted into pMD19T-hph vector containing the hygromycin-resistance gene by an orderly manner (Fig. 1a) for the construction of pKD-hph vector. Restriction sites EcoRV–Kpn1 and Spe1–Not1 are used to insert forward and reverse complemented RNAi fragment, respectively. The 788-bp EcoRV–Kpn1 fragment containing xyr1 cDNA sequence and reverse complemented Spe1–Not1 fragment were amplified by PCR from the total cDNA of Avicel-inducing T. reesei QM9414 and then were ligated into pKD–hph (Fig. 1b), generating pKD-hph–xyr1. The 905-bp cel7a cDNA sequence, 736-bp pyr4 cDNA sequences and 714-bp fab1 cDNA sequences, and their reverse complemented fragments, were inserted into pKD-hph in the same way as pKD-hph–xyr1, resulting in pKD-hph–cel7a, pKD-hph–pyr4 and pKD-hph–fab1, respectively. To construct P tcu1 –xyr1KD strain, the linearized pKD-hph–xyr1 vector with Ssp1 was used to transform T. reesei strain. Transformation of T. reesei was carried out essentially as described by Penttila [21]. Transformants were selected on minimal media containing 120 μg/mL hygromycin. Genomic PCR was used to verify correct integration events using a 2×T5 Super PCR Mix (TSE005, Beijing Tsingke Biotech Co., Ltd) as described in Additional file 1. Primers for plasmids construction and genomic PCR are also provided in Additional file 1. The knocking down of target genes was confirmed by comparing their mRNAs level in the media supplied with and without CuSO4.

Fig. 1
figure 1

Map of pKD-hph vector showing the main features and restriction sites used for plasmids construction. P tcu1 and T cel6a were used as promoter and terminator, respectively, for the expression of RNAi fragments. A cel5a intron was inserted between P tcu1 and T cel6a (a). Two reverse complemented RNAi fragments were inserted into the pKD-hph vector using EcoRV–Kpn1 and Spe1–Not1, respectively. The transcribed hpRNA fragments driven by the P tcu1 promoter can be processed by Dicer into siRNA, which then directs degradation of the target gene mRNA by RNAi mechanism. The transcription of RNAi fragment can be turned off when copper was present in the media (b)

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Enzyme activity and protein analysis

The activities of cellobiohydrolases (pNPCase) and β-glucosidases (pNPGase) were determined by measuring the amount of released p-nitrophenol using p-nitrophenyl-β-d-cellobioside (pNPC; Sigma, St. Louis, United States) and p-nitrophenyl-β-d-glucopyranoside (pNPG; Sigma) as substrates, respectively. The pNPC and pNPG activity assays were performed in 200 μL reaction mixtures containing 50 μL of culture supernatant and 50 μL of the respective substrate plus 100 μL of 50 mM sodium acetate buffer (pH 4.8) and then incubated at 45 °C for 30 min. One unit (U) of pNPCase or pNPGase activity was defined as the conversion of 1 μmol of substrate per minute under the test conditions as described previously [33]. The endo-glucanases and the filter paper activities (FPA) were determined by measuring the released reducing sugar with carboxymethylcellulose sodium salt (CMC; Sigma) and filter paper as substrates, respectively. Determination of the CMC hydrolytic activities was carried out at 50 °C in a 100 μL reaction mixture containing 50 μL of appropriately diluted culture supernatant and 50 μL of 0.5% (w/v) CMC sodium in 50 mM sodium acetate buffer (pH 4.8). The FPA assay was performed at 50 °C in a 200 μL reaction mixture including 50 μL of appropriately diluted culture supernatant and 150 μL 50 mM sodium acetate buffer (pH 4.8) with Whatman No. 1 filter paper as substrates. One unit (U) of CMCase or FPA was defined as the release of 1 μmol reducing sugar per minute under the test conditions [33]. Total secreted and intracellular proteins were determined using the Bradford protein assay with bovine serum albumin (BSA) as a standard. SDS-PAGE and Western blotting were performed according to the standard protocols and Cel7a was immunoblotted using a polyclonal antibody raised against amino acids 426–446 of the protein as previously described [34].

Quantitative RT-PCR (qRT-PCR)

Total RNAs were extracted using the Trizol reagent (Invitrogen, Grand Island NY, United States) and purified using the TURBO DNA-free kit (Ambion, Austin TX, United States) to eliminate the genomic DNA contamination according to the manufacturer’s instructions. Reverse transcription was performed using the PrimeScript RT reagent Kit (Takara, Japan) according to the instructions. Quantitative PCR was performed using SYBR green supermix (TaKaRa, Japan) on a Bio-Rad myIQ2 thermocycler (Bio-Rad, California, United States). Data were analyzed using the relative quantitation/comparative threshold cycle (ΔΔCT) method and were normalized to the endogenous gene actin. Primers for qRT-PCR are provided in Additional file 1. Three biological replicates were performed for each analysis and the results and errors are the mean and standard deviation (SD), respectively. Statistical analysis was performed using the Student’s t test analysis.

Designed culture procedure for investigating the fab1 gene function in T. reesei using copper-responsive RNAi system

In order to exclude the indirect effects of growth difference brought from pre-culture, we took P tcu1 –fab1KD strain as an example to redesign a culture strategy to characterize the function of fab1 in cellulase production in T. reesei. First, copper was added into MA media containing 1% glycerol as a sole carbon source in the first pre-culture for 36 h. Harvested mycelia were washed five times with media without a carbon source and then transferred to fresh MA media supplied without copper. After 12 h culturing, mycelia were harvested again and washed two times with media without a carbon source. Finally, mycelia were transferred to induced media containing 1% Avicel supplied without copper. As a control, P tcu1 –fab1KD strain was also culture in parallel with copper perpetually in the media to repress the expression of fab1 gene RNAi fragments. The mRNA level of tcu1 and fab1 were analyzed in the ending of first (Fig. 6b, c: sampling time S1) and second (Fig. 6b, c: sampling time S2) pre-culture by qRT-PCR. Besides, their mRNA abundance also was analyzed after mycelia grow under induced condition at 6 h (Fig. 6b, c: sampling time S3) and 12 h (Fig. 6b, c: sampling time S4), respectively. Cellulase production was assessed at 12, 24, 36, 48 60 and 72 h after the mycelia were transferred to the Avicel inducing media by measuring the FPA activity and SDS-PAGE analysis.

Results

Design of copper-responsive RNAi-mediated silencing system

The controllability of the P tcu1 promoter was incorporated into an RNAi-mediated silencing system in T. reesei. As shown in Fig. 1, gene-specific sequence was cloned as a tandem inverted repeat arranged on both sides of an intron from the cel5a gene to build synthetic hpRNA fragments, which was then inserted downstream of the P tcu1 promoter. The transcription of hpRNA fragments for target genes will result in the formation of double-stranded RNA that is recognized by Dicer and then produces siRNA to induce degradation of target mRNAs. In our present strategy, hpRNA fragments driven by P tcu1 are thus expected to down-regulate the transcript levels of the target gene when no copper ions were included in the media. Silencing can be reversed by adding back copper ions to mimic gene complementation.

Copper-responsive RNAi-mediated silencing of the prototrophic gene pyr4

The pyr4 gene encodes an orotidine 5′-phosphate decarboxylase which is involved in the uridine biosynthesis. Knockout of endogenous gene pyr4 in T. reesei showed that cells cannot survive unless uridine is present in the media [35]. Pyr4 is thus widely used as a screening marker in the genetic manipulation of T. reesei [22]. In order to test whether the RNAi-mediated silencing system can efficiently work in response to exogenous copper, the pyr4-specific hpRNA fragments were inserted downstream of the P tcu1 promoter in the pKD-hph vector, generating the pKD-hph–pyr4 plasmid. Transformants (P tcu1 –pyr4KD) were first selected on minimal media for resistance to hygromycin. Hyphal growth of selected P tcu1 –pyr4KD strains on minimal media agar plates with glucose as the sole carbon source was investigated. As showed in Fig. 2a, P tcu1 –pyr4KD spores barely germinated in glucose minimal media agar plate without addition of copper, which is also observed with the control strain QM9414–∆pyr4, demonstrating that the pyr4 gene was knocked down by the RNAi-mediated silencing system. Adding 20 μM copper (Fig. 2b) or 10 mM uridine (Fig. 2c) in the media rescued the growth, equivalent to the restored growth of QM9414–∆pyr4 on media only with 10 mM uridine (Fig. 2c). Under the above-tested conditions, the growth of QM9414–∆pyr4 was hardly affected by copper. These results revealed that the P tcu1 promoter controlled the transcription of pry4 RNAi fragment to knock down of pyr4 gene in response to the external copper.

Fig. 2
figure 2

Knockdown of pyr4 using P tcu1 -driven RNAi system was responsive to copper in agar plate. Equal amount of conidia spores from QM9414 and the P tcu1 –pyr4KD strain was inoculated on minimal media agar plate containing 2% (w/v) glucose as a sole carbon source. a No copper and uridine was present in the media. Twenty μM copper (b) and 10 mM uridine (c) were added into the minimal media agar plates, respectively

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Copper-controlled RNAi-mediated knockdown of cellulose-induced genes

To further test the effectiveness of the developed system, we selected two cellulose-induced genes for our proof-of-concept study. XYR1 is a critical activator for the transcription of cellulase and hemicellulase genes in T. reesei, deletion of which resulted in the abolishment of the induced production of nearly all (hemi)cellulases [36, 37]. The transcription of xyr1 itself has been also shown to be induced by cellulosic substrates such as Avicel and by lactose in T. reesei [38]. CEL7A is the major cellulase component produced by T. reesei and is shown to be tightly regulated by XYR1 [39, 40]. T. reesei QM9414 was first transformed with the pKD-hph–xyr1 and the cellulolytic activity of selected RNAi transformant was determined. As shown in Fig. 3a, the FPA was almost abolished in the P tcu1 –xyr1KD strain just as that of the ∆xyr1 strain, but remained at a similar level to that of QM9414 strain when 20 μM copper was present in the Avicel inducing media. In contrast to the P tcu1 –xyr1KD strain, only a slight increase of the extracellular FPA was observed with copper compared to that without copper for QM9414. The extracellular protein concentration of the P tcu1 –xyr1KD strain was also found to be dramatically reduced in the absence of copper, but maintained a similar level to that of the parental strain QM9414 in the presence of copper. SDS-PAGE analysis verified that the overall secreted proteins of the P tcu1 –xyr1KD strain under inducing conditions were severely reduced without copper, whereas no significant difference was observed with QM9414 when induced in the presence or absence of copper (Fig. 3c). To test whether the reduced FPA and extracellular protein were the results of down-regulation of xyr1 mRNAs, we determined the transcript level of xyr1 and that of cellulase genes cel7a and cel7b by quantitative qRT-PCR. The abundance of xyr1 mRNAs in the P tcu1 –xyr1KD strain was obviously reduced compared to that of QM9414 under Avicel inducing conditions without copper (Fig. 3f). In contrast, xyr1 mRNAs in the P tcu1 –xyr1KD strain were restored to a similar level to that QM9414 when copper ions were added to the Avicel inducing media (Fig. 3i). Similar to the case of ∆xyr1, the transcription of cel7a and cel7b in the P tcu1 –xyr1KD strain was severely reduced upon induction in the absence of copper (Fig. 3d, e). Adding 20 μM copper ions into the inducing media restored their transcription to levels comparable to those of the QM9414 strain (Fig. 3g, h).

Fig. 3
figure 3

The effect of xyr1 knockdown by copper-responsive RNAi-mediated silencing system. The extracellular FPA (a) and protein concentration (b) of the parental and P tcu1 –xyr1KD strains cultured on 1% (w/v) Avicel supplied with or without CuSO4 were determined as described in “Methods” section. SDS-PAGE analysis of the total extracellular protein accumulation (c) of the P tcu1 –xyr1KD and the parental strains cultured on 1% (w/v) Avicel supplied with or without CuSO4, respectively, at the indicated time points. qRT-PCR analysis of intracellular mRNA levels of the endogenous cel7a, cel7b, and xyr1 in parental and P tcu1 –xyr1KD strains was performed at the indicated time points with (g–i) or without (d–f) CuSO4. A significant difference (t test P < 0.05) was detected for the expression of cel7a, cel7b, and xyr1 in parental and P tcu1 –xyr1KD strains. Error bars are SD from three biological replicates

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Copper-controlled RNAi-mediated down-regulation of the highly transcribed cel7a was also tested. As shown in Fig. 4a, the parental strain QM9414 showed apparent hydrolytic halo on Avicel both with and without 20 μM copper. Similar hydrolytic halo was observed for the RNAi strain when 20 μM copper was included in the media. However, the P tcu1 –cel7aKD strain only displayed a very limited hydrolysis of Avicel when no copper was added. SDS-PAGE and Western blot analysis demonstrated that CEL7A was not detected in the extracellular supernatant of the P tcu1 –cel7aKD strain in the absence of copper upon induction (Fig. 4b). Together, these results demonstrated that highly expressed xyr1 and cel7a induced by Avicel could be successfully knocked down by the P tcu1 -driven RNAi approach in a controllable manner wherein the expression of XYR1 and CEL7A became responsive to the external copper levels in the media.

Fig. 4
figure 4

Knockdown of cel7a by the copper-responsive RNAi-mediated silencing system. Mycelial growth on double-layer agar plate containing 1% (w/v) Avicel supplied with or without copper (a). The parental and the P tcu1 –xyr1KD strains were cultured in Avicel-induced media without copper. The total extracellular proteins from both strains were analyzed by SDS-PAGE and Western blot at the indicated time points (b)

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Copper-controlled silencing of fab1 encoding phosphatidylinositol 3,5-bisphosphate kinase compromises cellulase production

Trichoderma reesei fab1 gene (Tr_78274) is annotated to encode phosphatidylinositol-3-phosphate 5-kinase homolog catalyzing the phosphorylation of phosphatidylinositol 3-phosphate (PtdIns(3)P) to yield phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2) [41, 42]. Deletion of fab1 in Saccharomyces cerevisiae has been reported to result in severe growth defect and exhibited enlarged vacuole probably due to the defect in vacuolar membrane recycling/turnover [43, 44]. Moreover, PtdIns(3,5)P2 has been reported to play a role in recruiting SAGA complex to the gal1 gene promoter to activate the gene transcription in S. cerevisiae [45]. We thus made multiple attempts to delete the fab1 homolog in T. reesei by HR for investigating its function on cellulase production but without success. This failure implied that fab1 may be essential for viability because we did not obtain strains with a complete removal of the endogenous fab1 gene (data not shown). Thus, we chose to conditionally knock down the expression of fab1 in T. reesei using the copper-responsive RNAi silencing strategy. As shown in Fig. 5a, the P tcu1 –fab1KD strain showed an approximately 80% decline in fab1 transcript abundance in the absence of copper upon Avicel induction, whereas no significant effect was observed when the RNAi strain was cultured with 20 μM copper. In addition, RNAi-mediated down-regulation of the fab1 gene did not result in a visible phenotype regarding mycelial growth and sporulation (Fig. 5e, f). To further evaluate the function of fab1 in cellulase induction, pNPCase, pNPGase and CMCase activities of the parental strain and the P tcu1 –fab1KD strain cultured on 1% (w/v) Avicel with or without copper were determined (Fig. 5b–d). The results revealed that the parental strain showed similar pNPCase, pNPGase and CMCase activity upon induction regardless of the presence or absence of copper, whereas the P tcu1 –fab1KD strain displayed significantly decreased hydrolytic activities in the absence of copper. Supplementing copper to the inducing media restored the production of the above cellulases in the RNAi strain. Interestingly, the observed defect in cellulase induction in the P tcu1 –fab1KD strain did not seem to occur at the transcription level since there was no significant reduction in transcript abundance of the cel7a and cel7b genes when cultured without copper (Additional file 1).

Fig. 5
figure 5

Knockdown of fab1 by copper-responsive RNAi-mediated silencing system. The abundance of fab1 mRNAs (a), extracellular pNPC (b), pNPG (c) and CMC (d) hydrolytic activity of the parental and P tcu1 –fab1KD strains cultured on 1% (w/v) Avicel supplied with or without copper were determined. Mycelial growth (e) and sporulation (f) of the parental TU6 and P tcu1 –fab1KD strains on agar plate containing 1% glucose and malt extract agar plate, respectively, supplied with or without copper were investigated

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In order to exclude any indirect effect by growth difference originating from the pre-culture on phenotype characterization, we also took the P tcu1 –fab1KD strain as an example to compare different culture strategies to verify the role of fab1 in cellulase production in T. reesei. As shown in Fig. 6a, the P tcu1 –fab1KD strain was pre-cultured for 36 h on glycerol with 20 μM copper. The transcription of the fab1 hpRNA fragment was repressed during this process with the P tcu1 –fab1KD strain displaying the same growth as the parental strain. After extensive washing, the pre-cultured mycelia were inoculated in fresh glycerol media with or without copper and incubated for 12 h, allowing the siRNAs targeting the fab1 mRNA to be accumulated during this period only in the absence of copper. Mycelia after this stage of growth were finally transferred into Avicel media with and without copper, respectively. The transcript abundance of tcu1 and fab1, filter paper activity, and extracellular protein concentrations of culture samples taken at specific time points (Fig. 6a: sampling time S1, S2, S3, S4) during the whole process were determined. As expected, the tcu1 promoter was immediately switched on when the pre-cultured mycelia were transferred to glycerol media without copper and maintained a relatively high-level expression after being transferred to the corresponding inducing conditions (Fig. 6b: sampling time S2). The transcript level of fab1 was, however, only slightly down-regulated at the sampling time S2 compared with that in the presence of copper (Fig. 6c: sampling time S2), indicating that this short period of culture before cellulase induction would contribute to the initiation of the RNAi process toward the target gene. After 6- (Fig. 6c: sampling time S3) and 12-h (Fig. 6c: sampling time S4) induction on Avicel, the abundance of fab1 mRNA reduced dramatically in the absence of copper, which was in sharp contrast with the no obvious decrease in fab1 mRNA quantity in the presence of copper. Correspondingly, the P tcu1 –fab1KD strain displayed significantly reduced extracellular FPA and protein accumulation upon induction without copper compared those with copper (Fig. 6d–f).

Fig. 6
figure 6

Redesigned culture strategy to verify the functional role of fab1 in cellulase production. Two culture procedures (a) were designed for functional study of fab1 in T. reesei using the copper-responsive RNAi-mediated silencing system. The abundance of fab1 (b) and tcu1 (c) mRNAs was quantified by qRT-PCR in the appointed sampling times. Filter paper activity was measured when mycelia were transferred into Avicel induction media at indicated time (d). Extracellular fermentation liquor (20 μL) of P tcu1 –fab1KD strain cultured on 1% Avicel supplied with (e) or without (f) copper was analyzed by SDS-PAGE

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Discussion

Trichoderma reesei is capable of secreting a large amount of proteins and represents a major workhorse for production of cellulases and other recombinant proteins as well [46]. Since its first isolation and the discovery for its astonishing potential to produce extracellular cellulases, extensive efforts have been made to further improve the production of T. reesei cellulases and thus to facilitate its industrial application through classical mutagenesis and screening, culminating in the isolation of strain RUT-C30 with a malfunction of the catabolite repressor CRE1 [47]. It is noteworthy that some strains used for the production of cellulases and hemicellulases on the industrial scale are descendants of RUT-C30 [48]. With the advent of fungal gene manipulation techniques, molecular biological strategies including HR-based gene deletion or overexpression were increasingly employed for strain improvement [49]. Such attempts have been best demonstrated by the introduction of β-glucosidases as well as other accessory proteins into T. reesei to act in synergistic way with T. reesei cellulases during biomass hydrolysis [5, 48, 50]. It is therefore not surprising that modern commercial cellulase preparations are usually based on genetically modified strains of T. reesei possessing rather high β-glucosidase activity [51]. In the genomic and post-genomic era, comparative genomic studies of T. reesei mutant strains resulted in the identification of potentially critical factors in lignocellulosic enzyme production and regulation, which further facilitate the rational design and construction of lignocellulosic enzyme hyper-production strains and the optimization of the enzyme profiles of T. reesei by genetic engineering [52]. This, however, requires a more versatile molecular tool box that enables easy manipulation of genes which is a prerequisite for strain engineering.

Although homologous recombination has been the major approach for producing knockout strains in T. reesei with varying levels of success, RNAi as a powerful tool in the functional genomic studies in eukaryotes could be employed for partial or condition-specific suppression of gene expression, particularly when gene deletion could be detrimental or even lethal. An ideal inducible RNAi system should be inactive in the un-induced state to prevent undesired gene silencing, and be rapidly induced to be able to repress target gene expression and also be reversible. The ability to manipulate gene expression in this way is thus anticipated to facilitate dissecting the functions of genes that give lethal or complex pleiotropic phenotypes in knockout mutants or stable RNAi transformant. In this study, we successfully knocked down the constitutively expressed pyr4 gene, Avicel inducing xyr1 and cel7a genes using the developed copper-controlled RNAi system. The RNAi strains displayed the same phenotype as that of deletion strains when copper was absent in the media by down-regulating the target gene expression, but behaved similarly as the parental strains when copper was present in the media. These data thus indicated that the developed responsive RNAi system could on the one hand readily knock down/off the target gene allowing the phenotypic characterization, whereas on the other hand it could mimic the complementation to exclude any unwanted effects resulted from the random integration of the hpRNA cassette by adding copper ions in the media. Compared with previously developed RNAi system with the constitutive or inducible promoter in T. reesei [31, 32], the present copper-responsive RNAi system does not depend on certain nutrition state and thus is applicable in any culture media. Importantly, the conditional silencing of the target gene allows the possibility to exclude any effect exerted by the differential growth between the RNAi strain and the control strain by specifically designed culture strategies. It should be pointed out that it would be convenient if the copper-controlled RNAi system could be turned on by directly adding specific copper chelators to the culture. Although our previous study demonstrated that trace amount of copper ions in the culture (< 200 nM) had hardly any effect on the expression of the tcu1 gene, the copper chelator bathocuproinedisulfonic acid (BCS) could only partially relieved the tcu1 repression and may therefore not be ideal for this system [28]. Nevertheless, we found that directly adding the copper to the culture can shut down the expression of hpRNA, simply washing the culture before transfer to a fresh medium without copper is an effective way to turn on hpRNA expression.

Taking advantage of the controllability of our copper-responsive RNAi-mediated gene silencing system, we investigated the function of fab1 gene for cellulase production, whose deletion was proven to be intractable with repetitive attempts. Our results showed that the knocking down of fab1 significantly reduced the cellulase production, whereas transcriptional analysis revealed that cellulase gene transcription was not affected. Thus, we speculated that RNAi-mediated down-regulation of the fab1 gene may interfere with other aspects of cellulase gene expression including protein sorting and transport rather than transcription. Considering that RNAi-mediated down-regulation of the fab1 gene showed no visible phenotypic deficiency regarding mycelial growth and sporulation, the failure to delete fab1 by homologous recombination was probably not due to the growth defect of the resultant mutant strain. Nevertheless, possibility cannot be ruled out that a low level of fab1 transcripts due to the incomplete silencing of fab1 was sufficient for the growth of the P tcu1 –fab1KD strain while the complete knockout of fab1 was lethal. The fab1 gene may thus play differential roles in T. reesei and the exact mechanism of fab1 on cellulose production requires further studies.

Previously, we developed a promoter replacement system, in which P tcu1 promoter was used to substitute the target endogenous promoter in situ [53]. Including cooper in the media results in the repression of target gene transcription while overexpression of target genes is achieved by excluding the copper in the media. The usefulness of this system has been illustrated by investigating the function of two subunits (Gcn5 and Ada2) of the putative Spt–Ada–Gcn5 acetyltransferase complex, whose knockouts were proven to cause severely defect in mycelia growth and spore formation [53, 54]. However, we noticed that the repression of some genes transcribed at a low level by P tcu1 promoter replacement system was not successful (data not shown), probably due to the slight leakage of the P tcu1 promoter. On the other hand, in the absence of copper, the high-level expression of the target genes in the promoter-replaced strain would sometimes complicate the phenotypic analysis. In the present study, we further developed a P tcu1 -driven RNAi-mediated silencing system to solve this issue. Thus, combining the P tcu1 promoter replacement system and the present P tcu1 -driven RNAi-mediated silencing system provides us the effective complementary tool set for the overexpression and knocking down of most genes in T. reesei for functional genomic studies.

Conclusion

In this study, we developed an RNAi-mediated silencing system driven by the P tcu1 promoter which is highly responsive to the copper ions. The developed RNAi system could readily knock down/off the target gene in the absence of copper allowing the phenotypical characterization and could mimic the complementation of the deficient strain simply by including copper in the media to exclude the unwanted effect that may result from the random integration of the hpRNA cassette. The copper-responsive RNAi-mediated silencing system is applicable on different nutritional states and represents a powerful tool for characterizing target gene functions in T. reesei.