Abstract
Coprinopsis cinerea is a model mushroom particularly suited to study fungal fruiting body development and the evolution of multicellularity in fungi. While microRNAs (miRNAs) are extensively studied in animals and plants for their essential roles in post-transcriptional regulation of gene expression, miRNAs in fungi are less well characterized and their potential roles in controlling mushroom development remain unknown. To identify miRNA-like RNAs (milRNAs) in C. cinerea and explore their expression patterns during the early developmental transition of mushroom development, small RNA libraries of vegetative mycelium and primordium were generated and putative milRNA candidates were identified following the standards of miRNA prediction in animals and plants. Two out of 22 novel predicted milRNAs, cci-milR-12c and cci-milR-13e-5p, were validated by northern blot and stem-loop reverse transcription real-time PCR. Cci-milR-12c was differentially expressed whereas the expression levels of cci-milR-13e-5p were similar in the two developmental stages. Target prediction of the validated milRNAs resulted in genes associated with fruiting body development, including pheromone, hydrophobin, cytochrome P450, and protein kinase. Besides, essential genes for miRNA biogenesis, including three coding for Dicer-like (DCL), two for Argonaute-like (AGO-like) and one for quelling deficient-2 (QDE-2) proteins, were identified in the C. cinerea genome. Phylogenetic analysis showed that the DCL and AGO-like proteins of C. cinerea were more closely related to those in other basidiomycetes and ascomycetes than to animals and plants. Taken together, our findings provided the first evidence of milRNAs in the model mushroom and their potential roles in regulating fruiting body development. Information on the evolutionary relationship of milRNA biogenesis proteins across kingdoms has also provided new insights into further functional and evolutionary studies of miRNAs.
Introduction
MicroRNAs (miRNAs), about 22 nucleotides (nt) in length, are one of the major groups of functional small non-coding RNAs (ncRNAs) besides piwi-interacting RNAs (piRNAs) and short interfering RNAs (siRNAs) [1,2]. Previous studies have demonstrated the presence of miRNAs in nearly all eukaryotic lineages and their essential roles in various biological processes [3–9]. In plants, miRNAs play roles in tissue morphogenesis, stress response and stem development [4]. In animals, miRNAs regulate cell proliferation and differentiation, apoptosis, and different metabolic pathways during developmental transition [5–9]. MiRNAs mediate post-transcriptional gene silencing to regulate gene expression through base pairing their seed region (2-7 nt at the 5’-end) to the untranslated region (UTR) or opening reading frame of their target genes [1,10]. Plant miRNAs mediate mRNA cleavage through perfect complementarity to their targets. On the contrary, miRNAs in animals bind to their targets through imprecise complementarity [10]. The first miRNA-like RNA (milRNA) in filamentous fungi was described in Neurospora crassa in 2010, more than a decade later than in animals and plants [11]. Although milRNAs have been subsequently discovered in other fungi, such as Sclerotinia sclerotiorum, Trichoderma reesei, Penicillium marneffei, Fusarium oxysporum, and Antrodia cinnamonmea, the potential roles of milRNAs in the developmental processes of mushroom forming fungi are still largely unknown [12–16].
Fungi possess a fascinating morphological diversity, ranging from the simplest unicellular yeasts to macroscopic mushrooms [17]. Coprinopsis cinerea, commonly known as the ink cap, is one of the most morphologically complex fungi with a well-characterized genome [18]. C. cinerea is also a model mushroom that is commonly used to study the developmental processes in higher basidiomycete fungi. Under nutrient depletion and normal day-night rhythm, the undifferentiated vegetative mycelium of C. cinerea undergoes dynamic genetic and physiological changes to form a multihyphal structure, known as the fruiting body, through hyphal aggregation and mycelial differentiation [19–21]. Fruiting body development of C. cinerea is a rapid but complex process, consisting of six main stages: mycelium, initials, stage 1 and 2 primordium, young fruiting body, and mature fruiting body [22]. The whole process can be completed within two weeks when the fungus is cultured on artificial media with optimal conditions [22,23]. Understanding the molecular regulatory mechanisms during fruiting body initiation and development is one of the major goals of mycological studies. The most significant transcriptomic switch has been demonstrated during the transition from mycelium to primordium, which represents a developmental transition from a loose, undifferentiated structure to a compact and well-organized multicellular body plan [24, 25].
Regulatory roles of miRNAs have been demonstrated in various multicellular organisms. In fungi, the key components of RNA regulatory networks and stage-specific milRNAs have also been reported [9, 11, 16, 26–31]. Some miRNAs in animals and plants are expressed in a stage-specific or tissue-specific manner, suggesting their potential roles in maintaining tissue specificity and functions [9, 32–35]. Here, we hypothesized that miRNAs also regulate developmental transition in the mushroom forming fungus C. cinerea. Prediction and identification of milRNAs and their targets in C. cinerea are feasible based on the published genome sequence data and transcriptomic profiles of the early developmental transition in C. cinerea [18, 24, 25]. In this study, we used high-throughput small RNA (sRNA) sequencing to computationally identify 22 putative milRNA candidates in the mycelium and primordium stages of C. cinerea. Two milRNAs, namely cci-milR-12c and cci-milR-13e-5p, were validated using northern blot analysis and their expression levels were examined by stem-loop RT-qPCR in both developmental stages. One of the milRNA candidates, cci-milR-12c, was found differentially expressed. Genes encoding putative Dicer-like (DCL), Argonuate-like (AGO-like) and quelling deficient-2 (QDE-2) proteins were identified in the C. cinerea genome [18]. Our results have provided evidence for the presence of milRNAs in C. cinerea, revealed their potential targets, and demonstrated a differential expression of milRNAs during the early developmental stages of the model mushroom. Our study has facilitated the understanding of the diversified regulatory roles of milRNAs and the molecular mechanisms of fruiting body development in higher basidiomycete fungi.
Materials and Methods
C. cinerea strains and growth conditions
The C. cinerea strain used for the identification of milRNAs and core milRNA biogenesis proteins is a dikaryon, mated from the monokaryotic strains J6;5-4 and J6;5-5 [36]. Two monokaryons were generated from single spore isolates of a dikaryon that had been backcrossed with the reference strain Okayama 7#130 for five generations. Besides, the homokaryotic fruiting strain #326 (A43mut B43mut pab1-1) was used in the siRNA-mediated Dicer knockdown analysis [37]. The strains were cultured on YMD medium containing 0.4% yeast extract, 1% malt extract, and 0.4% glucose with Bacto agar. Mycelia were cultivated on agar plates at 37 °C for about 45 days until the mycelium grew over the whole agar surface and reached the edge of plates. Fruiting body formation was induced by incubating the mycelium culture at 25 °C under a light/dark regime of 12/12 h [18,38,39]. The incubator was kept at a relative humidity > 60% for the production of fruiting bodies.
RNA isolation and sRNA sequencing
Samples were collected from two biological replicates for each developmental stage of C. cinerea. In brief, total RNA was extracted from mycelium (MYC) (4-5 days in the dark) and primodium (PRI) (~ 6-7 mm tall, 3 days in the light) using mirVana miRNA Isolation Kit (Ambion) and treated with TURBO DNA-free Kit (Ambion) according to the manufacturer’s instructions. Mycelia from four agar plates and 4-5 independent primordium structures were harvested and pooled to form one replicate. All samples were stored at −80 °C. Concentration and quality of RNA samples were checked using an Agilent 2100 Bioanalyzer. Using total RNA as the starting material, sRNA sequencing was performed by Macrogen (Korea) on a Hiseq 2500 platform (Illumina).
Bioinformatics analysis of sRNAs and prediction of milRNA candidates
Raw sequence reads were filtered to remove low quality reads with a Phred score lower than 20, adaptor and primer sequences, and reads shorter than 18 nt (Macrogen, Seoul, Korea). High quality reads were then used to build a non-redundant dataset in which reads identical in length and identity were clustered (Macrogen, Seoul, Korea). Clean unique reads were searched on Rfam v.9.1 to identify other types of small ncRNAs, such as rRNA, tRNA and snRNA (Macrogen, Seoul, Korea) [40]. Since previous studies have identified miRNAs derived from other small ncRNAs, clean clustered reads with 18-30 nt, including those aligned to tRNAs and rRNAs, were subsequently mapped to the C. cinerea genome (NCBI assembly accession: AACS00000000) using Bowtie and only perfectly matched sRNA reads were selected for milRNA prediction (Macrogen, Seoul, Korea) [41].
For milRNA candidate prediction, short clean reads ranging from 18-30 nt were first aligned to miRBase v.21 to categorize known miRNAs [42]. Then, an in-house Perl program was developed to identify the novel miRNAs. Since N. crassa demonstrated a wider range of precursor length than that in plants, the remaining mapped sRNA sequences were first extended on the genome to 51-150 bp in length to form a precursor-like hairpin structure [11]. Secondary structures of the extended sequence were computed by RNAfold in Vienna RNA package 2.0 with GU wobble base pair allowed. Putative milRNA candidates were selected using the following criteria: (1) sRNA that formed a hairpin structure with minimum free energy (MFE) of folding ≤ - 20 kcal/mol; (2) a RANDFOLD p-value of the predicted secondary structures < 0.01; and (3) with at least four reads [43,44,45].
Validation of milRNAs by northern blot analysis
Northern blot analysis of milRNA identification was performed according to the protocol of Kim et al. with double-labeled digoxigenin (DIG) oligonucleotide probes instead of locked nucleic acids (LNA) probes [46]. Briefly, total RNA (5-15 ug) from the two different developmental stages were resolved on a 15% denaturing polyacrylamide gel with 8M Urea in 1X TBE. The RNA gels were then transferred to Hybond-N+ (Amersham Biosciences) at 10-15 V (30-60 min) using a Trans-Blot SD semi-dry transfer cell (Bio-Rad). Cross-linking, hybridization and membrane detection were performed as previously described [46]. Cross-linking was performed using freshly prepared 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) reagent at 60 °C for 1 hr. Membranes were hybridized overnight in ULTRAhyb™ hybridization buffer (Ambion) with specific double DIG-labeled oligonucleotide probes synthesized by Integrated DNA Technologies at 37 °C. Sequences of the probes used against the putative milRNAs were as follows: ccin-milR-12c, 5’-AAAGGTAGTGGTATTTCAACGGCGCC-3’; ccin-milR-13e-5p, 5’-AGTCCCTACTAGGTCCCGAG-3’. Probe detection was performed using DIG luminescent detection kit according to the manufacturer’s instructions (Roche) and photoemissions were detected using the ChemiDoc-It Imaging System (Bio-rad).
Identification and phylogenetic analysis of DCL and AGO protein genes
One DCL protein (XP_002911949.1), two AGO-like proteins (XP_001837237.2, XP_001837864.2) and a QDE-2 protein (XP_001838344.1) were found in the predicted protein sequences of C. cinerea from GenBank (AACS00000000) [18]. For the phylogenetic analyses of the two main effector proteins in miRNA biogenesis, Dicer and AGO, corresponding protein sequences of animals, plants and some ascomycete fungi were downloaded from UniProt (http://www.uniprot.org/). Based on the annotated protein sequences of N. crassa DCL-1, DCL-2 (XP_961898.1, XP_963538.3) and QDE-2 (XP_958586.1), two other DCL proteins of C. cinerea (XP_001837094.2, XP_001840952.1), some ascomycete and basidiomycete fungi were identified using BLASTP against the JGI database (https://genome.jgi.doe.gov/) [11]. An E-value of ≤ 10E-10 and an identity ≥ 25% were used as the cutoffs in the BLASTP searches. Functional domains of the corresponding proteins in C. cinerea were predicted using Pfam and SMART [47, 48]. Phylogenetic trees of the proteins were constructed by the maximum likelihood method with 1000 bootstrap replicates using MEGA 7 [49].
Experimental quantification of milRNAs and biogenesis proteins by RT-qPCR
The sequence-specific TaqMan MicroRNA Assays and TaqMan small RNA Assays (Life Technologies) were used for RT-qPCR of cci-milR-12c and cci-milR-13e-5p, and the 5S rRNA (endogenous control), respectively. Reverse transcription was performed using TaqMan MicroRNA Reverse Transcription Kit (Applied Biosystems, Inc). Results from the 5S rRNA were used for normalization. cDNA was amplified in 20 uL reaction mixtures containing TaqMan Universal PCR Master Mix, no AmpErase UNG (Applied Biosystem) using standard qPCR conditions (95 °C for 10 min, followed by 40 cycles of 95 °C for 15 sec and 60 °C for 1 min) [50].
To examine the expression levels of the Dicer and AGO proteins in C. cinerea, total RNA was reverse transcribed to cDNA using Transcriptor First Strand cDNA Synthesis Kit (Roche Applied Science) with random hexamer primers. Real-time PCR analysis was performed using the SsoAdvanced Universal SYBR Green Supermix (Bio-rad), with 1 μl of 10 μM gene-specific forward and reverse primers (S1 Table). Thermal cycling was performed for 35-40 cycles with each cycle comprising polymerase activation at 95 °C for 30 sec, denaturation at 95 °C for 5-15 sec, and extension at 60 °C for 1 min. The relative expressions of DCL, AGO-like and QDE-2 proteins were normalized against 18S rRNA with forward primer (5′-GCCTGTTTGAGTGTCATTAAATTCTC-3′) and reverse primer (5′-CTGCAACCCCCACATCCA-3′). All the cycling reactions were performed in triplicate and the cycle threshold fluorescence data were recorded on an ABI 7500 Fast Real-Time PCR system (Applied Biosystems). The comparative Ct method (ΔΔCt) was exploited to calculate the relative expression levels of both validated milRNAs, DCLs, AGO-like and QDE-2 proteins. Statistical analysis was performed by Student’s t-tests. A P-value <0.05 was considered statistically significant.
Dicer-like proteins knockdown mediated by siRNAs
At least two sequence-specific siRNA targeting separate regions for each DCL mRNA were transfected into the stipe of primordium twice using needle and syringe to enhance the efficiency and effectiveness of knockdown [51]. The 5’-3’ sequences of the sense and antisense strands of synthetic Stealth siRNA duplexes (Invitrogen) of three DCLs are shown in S2 Table. The gene silencing effects were optimized through direct transfection of 8 μM siRNA. Briefly, primordium were first treated with synthetic siRNAs and incubated at 25 °C for 24 h. Then, the transfected primordia were treated with the same concentration of siRNAs and incubated for another 24 h. After the double transfection, total RNA samples of the control groups, untreated primordium and unrelated transfection (primordium with RNase-free water injection), and DCL knockdown strains were harvested. The remaining gene expressions of knockdown strains compared with the control groups were measured by quantitative real-time PCR using primers listed in S1 Table. Primers were designed to detect sequences between the sites of siRNA directed cleavage or at the target site of siRNA.
MilRNA target prediction and functional annotation
Since most miRNAs bind to the 3’-UTR of their target mRNAs to down-regulated their gene expressions, a database was constructed from the 1,000 bp downstream sequences of the stop codon of all genes in the C. cinerea genome for miRNA target prediction [18]. Since there are no general rules for the complementarity between fungal milRNAs and their targets and no prediction algorithms have been developed for fungi, three different types of software, PITA, miRanda and microTar, were used here to predict the potential targets of validated milRNAs in order to minimize false positive results [52–55]. Target genes were selected only when they were predicted by all of the three software.
Additional filtering steps were applied to select for putative targets with annotated biological functions using Gene Ontology (GO) terms, Eukaryotic Orthologous Groups (KOG) groups, KEGG orthologs (KO), and KEGG biological pathways [56,57,58]. Target genes that have been found to involve in fruiting body development were considered as putative targets [59]. GO terms of targets were assigned using BLAST2GO (version 2.4.2) with default parameters. KOG groups were assigned by RPS-BLAST (E-value cut-off of 1.00E-3). KO and KEGG biological pathways were assigned with the KEGG Automatic Annotation Server (KAAS) using all available fungal species as the representative gene set and the bidirectional best hits method (BBH). To further identify target mRNAs that likely interact with milRNA in vivo, annotated putative targets with similar expression patterns to the corresponding milRNAs between the two developmental stages were selected based on previously published microarray data of C. cinerea [25]. Functional targets with a fold change ≤ 0.5 and > 0.5 at MYC compared to PRI were considered as putative milRNA targets of cci-milR-12c and cci-milR-13e-5p, respectively.
Results
Identification of sRNAs in C. cinerea by high-throughput sequencing
The general features of sRNA species uncovered in MYC and PRI of C. cinerea are shown in Table 1. A total of 16,925,614 and 17,490,760 raw reads were obtained from MYC and PRI, respectively. A total of 1,354,235 and 1,379,040 unique sRNA reads (18-30 nt) were obtained from the MYC and PRI stages, respectively. A total of 152,835 and 135,648 rRNAs, and 15,890 and 12,280 tRNAs were included in the unique clean reads of the MYC and PRI samples, respectively. The major proportion of sRNA clean reads from both stages was 20-22 nt in length (Fig 1a) and had a strong preference for 5’ uracil (Fig 1b).
Prediction and identification of potential milRNAs in C. cinerea
Twenty-two putative milRNA candidates were identified in C. cinerea. Most of them appeared in both MYC and PRI, except cci-milR-1 and cci-milR-2, which were only presented in MYC. The read counts and sequences of the milRNAs are listed in Table 2. The 20 and 26 nt classes were the most abundant groups in the milRNA candidates (Fig 2a). Guanine dominated the 5’ end nucleotide with weak superiority (Fig 2b). Similar to canonical miRNAs in animals and plants, most of the milRNAs in C. cinerea were derived from the intergenic region (68%), with five from rRNA (23%) and two from exon (9%) (Fig 2c). As for the gene locations, half of the putative milRNAs dwelled on the assembled chromosomes (Table 2). Six putative milRNAs predicted in C. cinerea were located within a short distance on the U413 contig, similar to milRNAs in animals and plants, which usually appear in clusters [60].
Although no conserved milRNA of animals and plants was found in C. cinerea, one homolog of cci-milR-12c was identified in another mushroom forming basidiomycete fungus, Laccaria bicolor (GSE9784), suggesting important regulatory roles of milRNAs in mushroom forming fungi. Sequence of the cci-milR-12c precursor (pre-milR-12c) was BLAST searched against the L. bicolor EST database [61], and only sequences with no mismatches on the seed region of mature cci-milR-12c and with less than three mismatches to the downstream sequence of the seed region were regarded as homologs [62]. The absence of milRNA homologs of animals and plants in C. cinerea indicates evolutionary divergence of miRNA genes among these three kingdoms, coinciding with most of the fungal milRNAs [12,13,16].
Validation and characterization of milRNA expression patterns
Northern blot and RT-qPCR were used to validate the presence and to examine the expression levels of putative milRNAs in the two developmental stages. Two out of 22 milRNA candidates, cci-milR-12c and cci-milR-13e-5p, were verified using northern blot and their expression patterns during this developmental transition are shown in Fig 3. cci-milR-12c showed a higher expression in PRI (fold change >2), meaning that this milRNA candidate was differentially expressed in the early developmental stage. By contrast, the expression level of cci-milR-13e-5p in MYC was only slightly higher than that in PRI. The hairpin precursors of the two validated milRNAs are shown in Fig 4. Annotation of the gene loci of these two miRNAs indicated that the cci-milR-12c gene is located on an unassembled contig and cci-milR-13e-5p is derived from the intergenic region, based on the genome assembly data (AACS00000000) [17].
Although no annotated genes were identified in the locus of mature cci-milR-12c, there was a significant hit of pre-milR-12c to a eukaryotic rRNA sequence (accession: RF02543) when searching the precursor sequence on the Rfam database (E-value = 1.6e-26). Nucleotide sequence search also revealed that the pre-milR-12c sequence matched to the 28S rDNA locus of C. cinerea (E-value = 8e-62). Similar to rRNA-derived miRNAs found in human, the location of rRNA genes recovered here was distinct from that of the rRNA genes and cci-milR-12c might be generated during processing of the transcribed rRNA gene [63].
Identification of DCL, AGO-like and QDE-2 proteins and characterization of their expression patterns in MYC and PRI
Dicer and AGO are effector proteins known to participate in miRNA biogenesis in animals and plants [64]. QDE-2 protein is an AGO that has been identified to involve in the pre-miRNA cleavage in N. crassa and its homologs have also been found in various fungal species [11, 14, 15]. Based on homolog search of the N. crassa DCL, AGO-like and QDE-2 proteins against the C. cinerea genome and annotated protein sequences from Broad Institute, three DCL, two AGO-like and a QDE-2 protein were found in C. cinerea (Fig 5) [11, 59]. These proteins were named DCL-1 (CC1G_00230), DCL-2 (CC1G_03181), DCL-3 (CC1G_13988), AGO-like-1 (CC1G_00373), AGO-like-2 (CC1G_09846), and QDE-2 (CC1G_04788). The AGO-like genes CC1G_00373 (3,979 bp in length) and CC1G_09846 (3,457 bp in length) encode mRNAs that result in 897 and 981 amino acid residues, respectively. By contrast, the QDE-2 gene (CC1G_04788) is 3,438 bp in length and its resultant mRNA generates a 965 amino acid residue. All AGO family proteins predicted in C. cinerea contained at least one of the two characteristic domains of AGO protein: PAZ and Piwi domain. The mRNAs of Dicer protein homologs (CC1G_00230, CC1G_03181, CC1G_13988) encode 1499, 2074 and 1457 amino acid residues, respectively. Interestingly, only one of the C. cinerea DCLs (CC1G_00230) contained the PAZ domain, which is present only in mushroom-specific DCLs but not other fungal DCLs. Although PAZ is a conserved domain in both Dicer and many AGO family proteins, it cannot be found in one of our annotated AGO-like proteins (CC1G_00373) in C. cinerea (Fig 5) [65,66]. In general, the domain organization of DCL, AGO-like and QDE-2 proteins of C. cinerea was similar to that of N. crassa, except that there is no PAZ domain in AGO-like-1 (S1 Fig).
RT-qPCR was used to examine the mRNA expression levels of the protein homologs and the results are shown in Fig 6. DCL-1 and DCL-2 showed higher expression levels in PRI, however, DCL-3 was down regulated in PRI (Fig 6a). For the AGO homologs, the expression levels of AGO-like-1 and QDE-2 were significantly lower in PRI (Fig 6b). Similar to the expression levels of cci-milR-12c, DCL-1 and DCL-2, AGO-like-2 was expressed significantly higher in PRI than MYC. Therefore, DCL-1 or DCL-2 and AGO-like-2 are more likely involved in the biogenesis of cci-milR-12c. On the contrary, AGO-like-1 or QDE-2 and DCL-3 are more likely related to the higher expression of cci-milR-13e-5p in MYC.
Phylogenetic analysis of DCL and AGO homologs
Phylogenetic analysis of DCL and AGO proteins showed that both proteins duplicated early in the eukaryotic lineage and evolved independently in animals, plants and fungi (Figs 7 and 8). DCL and AGO homologs in C. cinerea were closely related to those in other basidiomycetes. Most of the mushroom forming fungi possess three DCLs, while other fungi contain only two DCLs. Besides, one DCL (CC1G_00230) of C. cinerea was grouped with DCLs of other mushroom forming basidiomycetes, namely Galerina marginata, Laccaria bicolor and Schizophyllum commune (Fig 7). These results suggest that Dicer proteins duplicated and diversified early in the eukaryotic lineage.
The expression levels of milRNAs in the DCL knockdown strains
Sequence-specific siRNA duplexes were used to knockdown individual DCL mRNA. The efficiency of knockdown of DCL mRNA following double transfection and the expression patterns of the two validated milRNAs in DCL knockdown strains are summarized in S2 Fig. Primordium transfected with siRNAs showed 60-80% knockdown of DCL mRNA transcript abundance comparing to the two control groups. A DIG-labelled probe specific for cci-milR-12c detected three bands in the control, with approximate sizes of 25/26, 40 and 50 nt on northern blot. The cci-milR-13e-5p-specific probe also revealed three bands on the blot, with sizes of about 20, 30, 40 nt. The ~20 nt bands were similar in size to the predicted cci-milR-12c and cci-milR-13e-5p, suggesting that they are the mature milRNAs. By constrast, the intermediate RNAs ~30-50 nt in size are likely the precursors of milRNAs (pre-milRNAs). However, the signals of the two mature milRNAs of DCL knockdown strains were similar to those of the controls. Given that the expression of DCL mRNAs was not completely abolished using knockdown, the roles of DCLs in milRNA biogenesis cannot be confirmed here.
Prediction and functional annotation of milRNA targets
Computational prediction of milRNA targets was carried out based on three different algorithms: miRanda, PITA and microTar, to minimize false-positive results. Each prediction algorithm predicted a few hundreds to thousands of target genes for each milRNA. miRanda and PITA rely on evolutionary conservation to select functional targets whereas microTar discerns milRNA targets by calculating the duplex energies without taking into account the conservation of miRNA targets [52–56]. The number of overlapped targets is shown in a Venn diagram (Fig. 9). There were 206 and 204 common targets of cci-milR-12c and cci-milR-13e-5p, respectively. Of these, 143 and 140 were annotated with functional GO, KOG terms or fruiting body related genes (data not shown). Given that the expression patterns of milRNA are similar to their targets and two milRNAs showed higher expression in MYC and PRI respectively, the expression levels of putative targets during the transition from MYC to PRI were used for the last filtering step. As a result, 15 and 133 functional genes were selected as the putative targets of cci-milR-12c and cci-milR-13e-5p, respectively (S3 Table).
Interestingly, both validated milRNAs targeted several fruiting body related genes (S3 Table). Cci-milR-12c targeted a fungal pheromone, hydrophobin and cytochrome P450. Cci-milR-13e-5p targeted protein kinases, transcription factors, heat shock protein, actin, cytochrome P450, and genes related to nucleic acid processing and cell cycle control. Altogether, these results suggest that milRNAs may play an important role for controlling the differential gene expressions and facilitating the cellular developments during the early developmental transition in C. cinerea.
Discussion
In this study, we constructed sRNA libraries and identified milRNAs of C. cinerea at two different developmental stages. Characteristics of C. cinerea milRNA populations similar to those in animals and plants and the presence of core proteins of miRNA biogenesis in C. cinerea suggest that milRNAs in mushrooms may be produced in similar pathways to those in animals and plants. Moreover, the functional analysis of milRNA targets demonstrates the potential regulatory roles of milRNAs in fruiting body development (S3 Fig).
The expression patterns of milRNAs give a hint on their biological functions across different biological processes. Here, we identified putative targets that exhibited a negative correlation in expression profiles with milRNAs during the transition from MYC to PRI, some of which were related to fruiting body formation. cci-milR-12c potentially controls mycelial development by targeting fungal pheromone and hydrophobin. Fungal pheromone is responsible for initiating septal dissolution and clamp-cell fusion during the transition from monokaryotic to dikaryotic state, whereas hydrophobin regulates morphogenesis in fungi, particularly in fruiting body development of basidiomycetes [22, 67, 68]. Besides, it has been reported that different sets of hydrophobins are employed by mushroom forming basidiomycetes in different developmental stages [68, 69]. On the contrary, cci-milR-13e-5p targeted protein kinases, cytochrome P450, laccase, actin, and genes related to nucleic acid processing. Protein kinase has been predicted to respond to nutrient depletion in fruiting body initiation, especially FunK1, which can only be found in multicellular fungi. In addition, the up-regulated heat shock proteins in PRI are response to the lower temperature for fruiting body development (25°C) than that of mycelial cultivation (37 °C) [18, 19, 70–73]. Therefore, cci-milR-13e-5p is more likely to regulate cellular metabolism during the early development transition, for instance, by supporting the dynamic structural changes and regulating oxidative phosphorylation, carbon metabolism and nucleotide metabolism, in response to an increased demand of DNA synthesis, energy production, protein synthesis and turnover from the mycelial to primordium stage [24]. Results suggest that milRNAs may play a role in controlling the drastic transcriptomic and morphological changes during fruiting body initiation.
Phylogenetic analysis results of DCLs, AGO-like and QDE-2 proteins and the fact that no miRNA homologs of animals and plants were identified in the C. cinerea genome, providing evidence to the claim that miRNAs may evolve independently among animals, plants and fungi [31, 74, 75, 76]. Our results also indicate an early duplication and diversification of Dicer proteins followed by a lineage-specific loss of PAZ domain in fungi. DCL-1 (CC1G_00230) is evolutionary closely related to other mushroom forming fungi and is the only DCL in C. cinerea that contains the PAZ domain, which has only been found in mushroom forming basidiomycetes. The PAZ domain recognizes the 3’ 2-nt overhang of pre-miRNA during miRNA biogenesis and the specific distance between the anchoring site of PAZ and RNase III domain is used to determine the milRNA product size [77]. However, this functional domain is absent in other fungal species, suggesting that different molecular mechanisms are adopted by DCLs without the PAZ domain to produce milRNAs with heterogeneity in length. Indeed, size heterogeneity of fungal milRNAs has been reported in N. crassa and F. oxysporum [11, 12]. Besides, homologs of cci-milR-12c were found in another mushroom, L. bicolor. These results suggest that milRNAs are produced in an alternative way among mushroom forming fungi and serve similar functions to regulate the development of multicellular structures in fungi.
Given that miRNAs are generally produced from a hairpin precursor by Dicer, the accumulation of pre-miRNAs can be detected in organisms with impaired Dicer function [1]. Change of miRNA expression patterns is an indicator of the participation of Dicer in its biogenesis. Although homologous recombination has been found in C. cinerea, gene knockouts are difficult to achieve due to the high efficiency of non-homologous DNA end joining [78]. Therefore, an alternative gene silencing method, dsRNA-mediated gene knockdown, which was successfully used in the study of C. cinerea strains #326 (A43mut B43mutpab1-1), was used in this study [79]. However, cci-milR-12c and cci-milR-13e-5p were still produced - corresponding RNA bands of these milRNAs were detected in northern blot, with a ~70% knockdown efficiency of DCLs. It is possible that milRNAs are efficiently produced, even when the expression levels of the DCLs are extremely low. Future works are needed to investigate the roles of PAZ-containing DCLs in milRNA biogenesis of mushrooms and to determine if the milRNA homologs play a regulatory role in other mushroom forming fungi.
Conclusions
Our findings have demonstrated differential post-transcriptional regulatory roles of milRNAs in different developmental stages of the mushroom forming fungus C. cinerea and identified the milRNA potential targets involved in fruiting body formation, providing new insights into the regulatory mechanisms of fruiting body development and the potential functions of milRNAs in fungi. Moreover, we have found putative core miRNA biogenesis proteins, Dicer and AGO, in the C. cinerea genome. Phylogenetic analysis showed that these proteins were more closely related to those in other fungal species than in animals and plants. However, the roles of DCLs, AGO-like and QDE-2 proteins in the biogenesis of C. cinerea milRNAs cannot be identified here. Altogether, these results serve as the foundation for further evolutionary developmental studies of fungi and contribute to the phylogenetic occurrence of miRNA-mediated regulatory system among different kingdoms.
Acknowledgements
We thank Dr. Hajime Muraguchi for sharing C. cinerea strains used in this study, Dr. Yi Liu for his insightful discussions on milRNAs and Mr. Tsz Kai Li for technical assistance.