Abstract
Members of the Yippee-like (YPEL) gene family are highly conserved in eukaryotes and are homologous to the Drosophila yippee gene. In this study, we functionally characterized two YPEL-homologous genes, MoYPEL1 and MoYPEL2, in the rice blast pathogen Magnaporthe oryzae using the deletion mutants ΔMoypel1, ΔMoypel2, and ΔΔMoypel1,2. The MoYPEL1 deletion mutant was significantly defective in conidiation and unable to undergo appressorium development; however, deletion of MoYPEL2 resulted in a significant increase in conidiation and the abnormal development of two appressoria per conidium. These data demonstrate the opposite roles of each member of the YPEL gene family during the development of M. oryzae. The double mutant was phenotypically similar to the ΔMoypel1 mutant in conidiation, but similar to the ΔMoypel2 mutant in appressorium development. Subcellular localization of the MoYPEL1 protein was dynamic during appressorium development, while the MoYPEL2 protein consistently localized within the nuclei during developmental stages. Our studies indicate that the two YPEL gene family members play distinct roles in the developmental stages of M. oryzae, furthering our understanding of disease dissemination and development in fungi.
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Introduction
Rice blast caused by the ascomycete fungal pathogen Magnaporthe oryzae is a threat to global rice production. This disease continues to be important with increased global population size and food demand1,2. In addition, the pathogen has a remarkable ability to destroy the whole rice plant including the leaf, collar, node, panicle base (neck), panicle, and sometimes root, unlike some pathogens that infect plants in a tissue-specific manner3. Magnaporthe oryzae is a polycyclic pathogen that enables the production of massive amounts of conidia (asexual spores) through multiple rounds of reproduction during the rice growing season. The nature of the pathogen implies a higher potential for epidemic incidence. The M. oryzae conidium develops a specialized infection structure called the appressorium at the tip of the conidial germ tube upon recognition of plant surface signals4. Generation of turgor pressure in the appressorium allows direct penetration of the plant epidermal cells. Following colonization of host cells, M. oryzae reproduces asexually to produce conidia that serve as a major dispersal unit and inoculum. Therefore, understanding the molecular events of conidiation and subsequent conidium-mediated disease development is important for developing novel strategies for plant protection.
Magnaporthe oryzae has served as a model for the study of the molecular events underlying fungal development, pathogenicity, and interaction with host plants. These cellular events are achieved by complex processes in which signaling pathways play a critical role in the genetic regulation and cross-talk with other signaling cascades for fungal development and pathogeneicty5. The cyclic AMP (cAMP)-associated protein kinase A signaling is known to regulate surface recognition and pathogenicity of M. oryzae6. A well-conserved mitogen-activated protein kinase (MAPK) pathway regulates appressorium development and subsequent invasive growth inside host plant cells in M. oryzae7,8,9. Glycogen and lipid mobilization to the appressorium is dependent on PMK1, a MAPK orthologous yeast Fus3/Kss1, following which glycogen and lipids are degraded via the protein kinase A pathway for turgor generation9. Mps1, a MAPK orthologous to yeast Slt2, is essential for cell wall integrity, appressorium penetration and invasive growth in M. oryzae10,11. Precise regulation of the cell cycle is critical, especially during infection-related development of M. oryzae, as in multicellular organisms12,13. The entry into mitosis and cell cycle arrest following mitotic entry and invasion of plant cells, respectively, are essential for appressorium differentiation14,15. Further investigation uncovered that two independent S-phase cell cycle checkpoints are required for appressorium-mediated plant infection in M. oryzae16. Recently, it was shown that CDC14 in M. oryzae (MoCDC14), which is orthologous to the phosphatase CDC14 in Saccharomyces cerevisiae17,18, plays a key role in septation and nuclear distribution, which are linked to the proper regulation of appressorium formation, conidiation, and growth in M. oryzae19.
In this study, we set out to elucidate the roles of the members of the Yippee-like (YPEL) gene family in the development and pathogenicity of M. oryzae, which are homologous to the first identified Drosophila Yippee gene coding for a protein with a putative zinc finger-like metal binding domain20. The YPEL family, which consists of one member in yeast and five members in mammals, is highly conserved across eukaryotic taxa21,22. Members of the YPEL gene family have been shown to be associated with various cellular processes including the cell cycle, senescence, and development in mammals23,24,25. Recently, the MOH1 gene, which is orthologous to the Drosophila Yippee protein, was shown to be involved in apoptosis induced by DNA damage in S. cerevisiae26. However, the YPEL family remains uncharacterized in filamentous fungi, which prompted us to investigate the functional roles of the phytopathogenic fungus M. oryzae. Our analysis in silico led to the identification of two YPEL genes (named MoYPEL1 and MoYPEL2) in M. oryzae, unlike in yeasts, which have only one. Here, we investigated the functional roles of the MoYPEL1 and MoYPEL2 genes during M. oryzae morphogenesis and disease development through targeted gene deletion. Our study indicates important and distinct roles of the YPEL gene family in disease dissemination and development in the phytopathogenic fungus M. oryzae.
Results
Phylogenetic analysis of MoYPEL proteins
Magnaporthe oryzae was found to contain two YPEL genes based on BLAST search of the genome database (http://fungi.ensembl.org) using conserved sequences (IPR034751) of the Yippee protein. The resulting sequences were then aligned with the sequences of the five human YPEL genes and the yeast MOH1 gene to reveal phylogenetic relationships (Supplementary Fig. S1)22,26. Based on phylogenetic analysis, the two M. oryzae genes were named MoYPEL1 (MGG_06263.7) and MoYPEL2 (MGG_00255.7). MoYPEL1 forms a clade together with human YPEL5 and yeast MOH1 with 42% and 49% sequence identities, respectively (Supplementary Table S1). MoYPEL2 forms a separate lineage with the remaining human YPELs, while it shares 42% and 40% identity with the human YPEL4 and MoYPEL1, respectively. Phylogenetic analysis of MoYPELs and related proteins in fungal taxa showed that MoYPEL1 forms a separate lineage within ascomycetes in which it shares the highest identity of 88% with the E3QQW8 protein of Colletotrichum graminicola (Fig. 1 and Supplementary Table S1). In clade I, MoYPEL1 and the other related proteins are distantly related to yeast MOH1. MoYPEL2 shares relatively low similarity with ascomycete proteins, among which, 55% identity with the E3QBW1 protein of C. graminicola was the highest value. We found that filamentous ascomycetes have two YPEL-related proteins, unlike S. cerevisiae. The two separate lineages and low similarity between MoYPEL1 and MoYPEL2 may imply potentially different functions of the two proteins in the cellular events of M. oryzae. Alignment of YPEL-related proteins revealed that homologs of MoYPEL1 have consensus sequences, which is consistent with consensus sequence VII (C-X2-C-X19-G-X3-L-X5-N-X13-GXH-X6-C-X2-C-X4-GWXY-X10-K-X6-E) reported in a previous study (Fig. 2)20. MoYPEL2-related proteins in clade II also have an additional sequence expansion that is variable from X5 to X36 at position X5 of consensus sequence VII. All of the fungal YPEL proteins contain a nuclear localization signal (NLS) at the C-terminus of this domain.
Subcellular localization of MoYPEL proteins
To further understand the potential cellular roles of MoYPEL proteins, we generated transformants expressing MoYPEL1:sGFP and MoYPEL2:sGFP fusion proteins by transforming protoplasts of a transformant expressing a histone H1:RFP fusion protein27,28. The transformants were confirmed to be phenotypically similar to wild type (Supplementary Table S2). The MoYPEL1:sGFP fusion protein was initially distributed uniformly in the cytoplasm and nuclei of conidia (Fig. 3A). Interestingly, a marked increase in aggregation of the MoYPEL1 signal was quickly observed next to nuclei in conidium cells, which were subsequently distributed diffusely in the cytoplasm next to nuclei. As a germ tube emerged, the MoYPEL1 signal translocated out of the nucleus as assembled particles at the third conidium cell. Prior to mitosis, the assembled forms of the MoYPEL1 signal were maintained not only in the third cell, but also in an appressorium initial. Finally, the aggregated MoYPEL1 signal in the appressorium was diffusely distributed similar to the distribution in conidium cells following mitosis. Unlike the dynamic localization of the MoYPEL1:sGFP signal during appressorium development, the MoYPEL2:sGFP signal colocalized stably with nuclei not only during vegetative growth, but also during appressorium development (Fig. 3B). The differing subcellular localizations of the MoYPEL proteins suggest their distinctly different roles during M. oryzae morphogenesis and disease development.
Roles of the MoYPEL genes in vegetative growth
To determine the functional role of MoYPEL genes in growth, we measured vegetative growth on solid media including complete medium (CM), V8 medium, and minimal medium (MM). The ΔMoypel1 mutant exhibited a significant defect on all three nutrient conditions while the growth of ΔMoypel2 was indistinguishable from that of the wild type (Fig. 4A). The vegetative growth of the double mutant ΔΔMoypel1,2 was also similar to that of the wild type. Compared to the growth of the wild type, growth of the ΔMoypel1 mutant was reduced by about 23% on CM and V8 medium, and more severely by 50% on MM. To further investigate the reduced vegetative growth in the ΔMoypel1 mutant, hyphae of the mutant were stained with calcofluor white (CFW) to test septation and hyphal morphology during vegetative growth. Unlike the wild type and other mutants, increased septation was observed in the ΔMoypel1 mutant (Fig. 4B), although the hyphal morphology of the mutants was similar to that of the wild type. The average distance of the hyphal compartments of the ΔMoypel1 mutant was 29.3 µm, while the wild type, ΔMoypel2, and ΔΔMoypel1,2 strains were 135, 118.9, and 131.4 µm, respectively, as shown in Fig. 4C. This result suggests that the reduced vegetative growth was due to shortened hyphal compartments, which was a result of the increased septation in the ΔMoypel1 mutant.
Roles of the MoYPEL genes in conidiation
Because conidia serve as a major inoculum and propagule in many fungal pathogens, we assessed association of the MoYPEL genes with conidiation by measuring the production of conidia. Microscopic observation revealed that the ΔMoypel1 and ΔΔMoypel1,2 mutants showed considerably impaired ability to produce conidia compared with that of the wild type (Fig. 5A). However, the ΔMoypel2 mutant showed an increased ability with more dense conidia. Quantitative measurement of conidium production indicated that the ΔMoypel1 and ΔΔMoypel1,2 mutants produced significantly less conidia by 22% and 27%, respectively, but the ΔMoypel2 mutant produced significantly more conidia by 151%, compared with the wild type (Fig. 5B). Such abnormality of the ΔMoypel1 and ΔMoypel2 mutants was rescued in the complemented transformants Moypel1c and Moypel2c, respectively. These results suggest that each of MoYPEL genes plays a distinct and opposite role in the regulation of conidiation.
To examine the effect of MoYPEL deletion on the expression of genes important for conidiation in M. oryzae, we measured gene expression in each deletion mutant using quantitative RT-PCR (qRT-PCR) (Table 1). Differences in gene expression were observed in each deletion mutant (Fig. 6A). Unlike the expression of MoPLC3, MoPLC1 was significantly upregulated only in the ΔMoypel2 mutant, and MoPLC2 expression was upregulated in the ΔMoypel1, ΔMoypel2, and ΔΔMoypel1,2 mutants. Transcripts of MoAPS1, ACR1, MoCON6, CON7, MoCON8, MoFLBA, Flb3, and Flb4 were significantly increased at different levels in both the ΔMoypel1 and ΔMoypel2 mutants, among which the MoCON6, MoCON8, MoFLBA, Flb3, and Flb4 genes were also upregulated in the ΔΔMoypel1,2 mutant. The CPKA, PMK1, and MAC1 genes were highly expressed in the ΔMoypel1, ΔMoypel2, and ΔΔMoypel1,2 mutants. The different levels of gene expression in the ΔMoypel1 and ΔMoypel2 mutants suggest that the MoYPEL1 and MoYPEL2 genes play distinct roles in M. oryzae conidiation.
To understand the impact of signaling pathways on the expression of MoYPEL genes, we measured expression of the MoYPEL genes in signaling pathway-related mutant backgrounds (Table 2 and Fig. 6B). The Δmac1 mutant lacks an adenylate cyclase, the Δpmk1 mutant lacks an MAPK, and the ΔMoplc2 mutant lacks phospholipase C. MoYPEL2 was significantly induced in all three mutants, although the expression of MoYPEL1 was almost unchanged in these mutants. Both MoYPEL genes were significantly downregulated in the phospholipase C mutants ΔMoplc1 and ΔMoplc3, but not in the ΔMoplc2 mutant, which supports the different roles of the MoPLC genes, as previously reported23. This suggests that the regulation of MoYPEL expression may be associated with Ca2+ and cAMP-dependent signaling pathways.
Roles of the MoYPEL genes in appressorium development
As appressorium-mediated penetration plays a key role in M. oryzae, we tested the ability of the tested strains to develop appressoria upon sensing an inductive hydrophobic surface. This experiment revealed that ΔMoypel1 was defective in appressorium development on the hydrophobic surface, while almost all conidia from wild type and Moypel1c developed appressoria (Fig. 7A,B). Next, we investigated the effect of exogenous cAMP on appressorium development of the ΔMoypel1 mutant.
Almost all conidia from wild type developed appressoria on both hydrophobic and hydrophilic surfaces with treatment of 5 μM exogenous cAMP. Treatment with exogenous cAMP markedly restored appressorium formation in the ΔMoypel1 mutant; Approximately 57.3% and 59.3% of the ΔMoypel1 conidia formed appressoria on the inductive and non-inductive surfaces, respectively, with exogenous cAMP treatment (Fig. 7A,B). These results indicate that the ΔMoypel1 mutant may be defective in sensing signals of hydrophobic surface and intracellular cAMP signaling pathway for appressorium development. Unlike the defect of ΔMoypel1 in appressorium development, the ΔMoypel2 mutant produced a large number of instances of two appressoria on two separated germ tubes emerged from conidia (Fig. 7C). The different sizes of the two appressoria in the ΔMoypel2 mutant are indicative of the subsequent development of two appressoria. Similar to the ΔMoypel2 mutant, the ΔΔMoypel1,2 mutant also produced two appressoria. At 48 h, 10.3% and 16.3% of the ΔMoypel2 and ΔΔMoypel1,2 mutants, respectively, formed two appressoria compared with 2.3% and 2.0% of the wild type and Moypel2c (data not shown). During prolonged incubation (72 h), these percentages increased dramatically to 39.3% and 47.7% of the ΔMoypel2 and ΔΔMoypel1,2 mutants, respectively (Fig. 7D). The percentage of two appressoria in ΔMoypel2 and ΔΔMoypel1,2 was unaffected with treatment of exogenous cAMP. This result suggests that MoYPEL2 plays a distinct role in the regulation of appressorium development, given that a defect of ΔMoypel1 mutant in appressorium development is recovered with exogenous cAMP treatment.
Consistent with the roles of MoYPEL genes in appressorium development, changes in transcription of appressorium-related genes were detected as shown in Fig. 6A. These include the MoHOX7, MoPLC2, CPKA, PMK1, and MAC1 genes, which were significantly upregulated at different levels in the ΔMoypel1, ΔMoypel2, and ΔΔMoypel1,2 mutants, although MoPLC1 was highly upregulated only in the ΔMoypel2 mutant. In addition, expression changes of the MoYPEL genes in the signaling pathway-related mutant backgrounds (Table 2 and Fig. 6B) suggest the possibility that the Ca2+ and cAMP-dependent signaling pathways are linked to MoYPEL-mediated appressorium development.
Roles of the MoYPEL genes in pathogenicity
To evaluate the involvement of the MoYPEL genes in pathogenicity, conidial suspension was sprayed onto susceptible rice seedlings (cv. Nakdongbyoe). The wild type caused severe necrotic lesions, but the ΔMoypel1 and ΔΔMoypel1,2 mutants were non-pathogenic (Fig. 8A). The ΔMoypel2 mutant appeared slightly less severe than the wild type. The defects of the mutants were rescued in the corresponding complemented transformants. To further characterize the role of MoYPEL genes in pathogenicity, we inoculated hyphal agar plugs and conidial drops on both intact and wounded sites of detached leaflets of the rice cultivar. Consistent with the spray assay, inoculation of hyphal plugs and conidial drops from the wild type and the ΔMoypel2 mutant strains developed severe lesions, but no disease symptoms were observed with the ΔMoypel1 mutant on intact sites. The ΔΔMoypel1,2 mutant resulted in fewer reduced lesions from hyphal agar plugs on intact sites, but not from the conidial drops (Fig. 8B). Unlike the inoculations on intact sites, the wounded inoculations of both hyphal plugs and conidial drops from all strains developed severe disease symptoms. This result suggests that the failure of the ΔMoypel1 and ΔΔMoypel1,2 mutants with conidium inoculation are due to an inability to penetrate, rather than a defect in the ability to undergo invasive growth inside host cells. When rice sheath cells were inoculated with conidial suspension, the wild type and ΔMoypel2 mutant developed appressoria and exhibited subsequent invasive growth (Fig. 8C). In contrast, the ΔMoypel1 mutant was able to develop appressoria but unable to undergo appressorium-mediated penetration and invasive growth on rice sheath cells. A further investigation of pathogenic development of ΔMoypel1 and ΔΔMoypel1,2 mutants on rice sheath cells with treatment of exogenous cAMP had no effect on the defects of the two mutants in appressorium-mediated penetration (Fig. 8C). These results indicate that MoYPEL1 is essential for appressorium-mediated penetration, possibly, independent of cAMP-related pathway, and MoYPEL2 is necessary for the full virulence in M. oryzae. The complemented transformants of these mutants were successful in penetration and invasive growth.
Because the ΔMoypel1 mutant developed appressoria on rice sheath cells, but not on artificial hydrophobic surface (Fig. 7), we tested host factors inducing appressorium development by exogenously adding two known host inducers, a cutin monomer, 1,16-hexadecanediol and a primary alcohol, 1-octacosanol on both hydrophilic and hydrophobic surfaces29,30. Compared to those of the wild type and Moypel1c, the ΔMoypel1 mutant was still defective in appressorium development in the treatment of 10 µM 1,16-hexadecanediol (Fig. S3). However, 54.3% and 37% of conidia in ΔMoypel1 mutant developed appressoria on the hydrophobic and hydrophilic surfaces, respectively, with the treatment of 10 mM 1-octacosanol, suggesting that the ΔMoypel1 mutant is partially able to response to certain host signals such as a primary alcohol, 1-octacosanol present on host cells. These results indicate that MoYPEL1 is involved in sensing certain physical and chemical signals such as hydrophobicity and a cutin monomer for appressorium development.
Discussion
Although the YPEL gene family exists in all eukaryotes, functional roles of YPEL genes have been mostly uncharacterized in eukaryotic organisms, including filamentous phytopathogenic fungi22. This prompted us to elucidate the detailed roles of MoYPEL genes in the pathogenic development of the rice blast pathogen M. oryzae. In this study, filamentous fungi, unlike yeast, were revealed to contain two YPEL genes26. Our phylogenetic analyses revealed the distant relatedness of fungal YPEL genes with the yeast MOH1 gene, which is homologous to the human YPEL5 gene, raising the possibility that the fungal YPEL genes play different roles than the apoptotic role of MOH126. Given that each member of a gene family has evolved toward divergence in sequence and function, separate lineage formation of the fungal YPEL genes would support functional differences of the different members of the fungal YPEL gene family. Our findings support the conclusion that each member of the YPEL gene family plays distinctly different roles in M. oryzae development and pathogenicity.
The disparate subcellular localization patterns of MoYPEL:sGFP fusion proteins are intriguing. Stable nuclear localization of the MoYPEL2 fusion protein during different developmental stages of M. oryzae was consistent with the presence of an NLS at the C-terminus. In addition, this expression pattern may suggest the constitutive expression of the MoYPEL2 protein at the translational level. Unlike MoYPEL2 localization, subcellular localization of the MoYPEL1:sGFP fusion protein was dynamic during appressorium development. MoYPEL1 proteins were initially distributed in both the cytoplasm and nuclei of conidia. Subsequent subcellular translocation of MoYPEL1 protein appears associated with appressorium development. During germ tube and appressorium formation, the MoYPEL1 protein translocated out of the cytoplasm and nucleus as assembled particles, which were maintained until mitosis. Given that YPEL5, which is homologous to MoYPEL1, is involved in cell cycle progression in monkey cells21, it has been speculated that MoYPEL1 may be involved in the cell cycle during appressorium development, until further investigation shows MoYPEL1 to colocalize with cellular organelles in mitosis.
To characterize the functional roles of MoYPEL genes, we generated the knockout mutants ΔMoypel1, ΔMoypel2, and ΔΔMoypel1,2, which exhibit pleiotropic defects in morphogenesis and disease development in M. oryzae. Notably, the MoYPEL gene family was shown to be important especially for disease dissemination and development in M. oryzae. Conidium production was highly reduced in the ΔMoypel1 mutant, but increased in the ΔMoypel2 mutant, indicating the opposite regulation of MoYPEL genes in conidium production in M. oryzae. Interestingly, the double mutant ΔΔMoypel1,2 was similar to the ΔMoypel1 mutant in conidium production, suggesting that MoYPEL1 is downstream of MoYPEL2 in the proper regulation of conidium production. Detailed biochemical functions of YPEL proteins remain unknown in eukaryotes including fungi. However, a zinc-binding motif (two cysteine pairs) and NLS motifs of MoYPEL proteins imply potential roles in protein-protein interactions and transcriptional regulation. The nuclear localization of MoYPEL proteins and transcriptional changes of several conidiation and/or appressorium-related genes in MoYPEL mutants may reflect the involvement of MoYPEL proteins in transcription regulation. Interestingly, the MoYPEL genes were significantly changed in deletion mutants of signaling regulators. Unlike MoYPEL1, MoYPEL2 was significantly upregulated in the three mutants Δmac1, Δpmk1, ΔMoplc2, suggesting that the regulation of MoYPEL2 expression is associated with cAMP, MAPK, and Ca2+-dependent signaling pathways. However, a significant downregulation of the two MoYPELs in ΔMoplc1 and ΔMoplc2 mutants may suggest the interrelated but different roles of MoPLC genes not only in MoYPEL expression but also development regulation in M. oryzae, as previously suggested31,32. The subcellular translocation of MoYPEL1 from nuclei and the cytoplasm during appressorium development may also reflect the interaction of MoYPEL1 with unknown protein(s) involved in MoYPEL1 translocation and function during appressorium development. In animal COS-7 cells, YPEL5 has been shown through coimmunoprecipitation to physically interact with Ran-binding protein in the microtubule-organizing center (RanBPM)21.
Appressorium development is a key event for disease development in M. oryzae. MoYPEL genes was proven to be important for this process. The ΔMoypel1 mutant was defective in sensing the hydrophobic surface for appressorium development, which was restored by exogenous cAMP treatment, indicating that such defect could be bypassed with complemented appressorium development of the ΔMoypel1 mutant on both inductive and non-inductive surfaces. The fact that the ΔMoypel1 mutant formed appressoria on rice sheath cells, as not observed on the hydrophobic surface, is an indicative of its ability to recognize a host inducer of appressorium development. Our subsequent assays revealed that the ΔMoypel1 mutant partially recognized a primary alcohol, 1-octacosanol, but not a cutin monomer, 1,16-hexadecanediol. Taken together, these results indicate that MoYPEL1 was involved in sensing chemical and physical signal cues for appressorium development in M. oryzae. Unlike the ΔMoypel1 mutant, abnormal development of two appressoria per conidium in the ΔMoypel2 mutant indicates the opposite role in appressorium development in M. oryzae. The phenotype of the ΔMoypel2 mutant is similar to those of deletion mutants for MoPLC2 and MoPLC3, as shown in our previous study31. Considering that the expression of MoYPEL genes is modulated in deletion mutants of MoPLC genes, functional roles of MoYPEL genes could be associated with Ca2+-mediated regulation of appressorium development. As expected, the ΔMoypel1 and ΔΔMoypel1,2 mutants were non-pathogenic due to their inability to penetrate plant cell walls and initiate invasive growth. However, the ΔMoypel2 mutant developed a slight reduction in disease symptoms following penetration and invasive growth in plant cells. Collectively, our study demonstrates that MoYPEL genes play important roles in growth, conidiation, and appressorium development in M. oryzae.
Methods
Fungal strains and culture conditions
Magnaporthe oryzae wild type strain KJ201 and fungal transformants generated in this study were routinely cultured on oatmeal agar plates (OMA; 5% oatmeal and 1.5% agar powder) or V8 agar plates (V8; 8% V8 juice and 1.5% agar powder) for 10 days at 25 °C, under constant fluorescent light to promote conidiation. Mycelia used for genomic DNA and total RNA extraction were prepared by growing the relevant strains in liquid CM (0.6% yeast extract, 0.6% casamino acids, and 1% sucrose) for 3 days at 25 °C with agitation (150 rpm), or directly obtained from TB3 agar medium (0.3% yeast extract, 0.3% casamino acids, 1% glucose, 20% sucrose, and 0.8% agar powder).
Preparation of protoplasts
Magnaporthe oryzae mycelia were cultured in liquid CM for 2–3 days and harvested with a bottle top filter, as described by Parsons et al.33. Briefly, mycelia were washed twice and resuspended in 20% sucrose. Lysing enzymes from Trichoderma harzianum (Sigma-Aldrich, St. Louis, MO, USA) was added to the mycelial suspension (5 mg/ml). The protoplasts were separated from the mycelia by filtration through two layers of Miracloth (Calbiochem, La Jolla, CA, USA). After centrifugation of the protoplast suspension at 5,000 rpm for 15 min at 4 °C, the protoplast pellet was twice washed with STC buffer (20% sucrose, 0.05 M Tris/Cl pH 8.0, and 0.05 M CaCl2), and re-suspended after centrifugation with STC buffer to make a final concentration of 5 × 107 protoplasts ml−1.
Bioinformatics tools
The protein sequences were obtained from the National Center for Biotechnology Information (NCBI); homology search of protein sequences was performed using the BLAST algorithm. Domain architectures were drawn using InterProScan software34. The phylogenetic tree was generated with a neighbor-joining method with 1,000 bootstrap replicates with MEGA7 software (http://www.megasoftware.net)35. Amino acid sequences were aligned using BioEdit Ver. 7.0.5 software (http://www.mbio.ncsu.edu/BioEdit/bioedit.html).
Vector construction and fungal transformation
To investigate the functional roles of MoYPEL genes, we generated the targeted gene knockout mutants ΔMoypel1 and ΔMoypel2 using homology-dependent gene replacement as illustrated in Figure S2. Targeted deletion constructs for MoYPEL1 and MoYPEL2 was made by a modified double joint PCR36. Each fragment corresponding to 1.5 kb upstream and downstream of MoYPEL1 and MoYPEL2 was amplified with primers 5F/5R and 3F/3R (Supplementary Table S3), respectively. A 1.5-kb HPH cassette was amplified with the primers HPHF/HPHR from pBCATPH, which contains the hygromycin phosphotransferase gene37. The three PCR products were fused by rounds of fusion PCR, and the final deletion construct was amplified with the nested primers NF/NR. Protoplast suspension (5 × 107 protoplasts ml−1) was used for a polyethylene glycol-mediated transformation of M. oryzae38,39. Briefly, the transformation was conducted by incubating 0.2 ml of protoplasts with DNA (2–3 µg the deletion construct) for 30 min at room temperature followed by the addition of 1 ml of PTC (40% PEG, 20% sucrose, 0.05 M Tris/Cl pH 8.0, 0.05 M CaCl2). The contents were mixed with 3 ml of TB3 (20% sucrose, 1% glucose, 0.3% yeast extract) regeneration medium. The mixture was plated TB3 agar plates supplemented with hygromycin (200 ppm). Hygromycin-resistant transformants were screened by PCR with the primers SF/SR. For the selected transformants, genomic DNA was extracted using the quick and safe method40. Targeted deletion was confirmed with Southern blot hybridization and RT-PCR. For complementation, a genomic copy of the targeted gene was amplified from wild type genomic DNA using the primers cmF/cmR. The amplicon was used for co-transforming protoplasts of the deletion mutant with the pII99 vector containing a geneticin-resistance cassette41. Complementation mutants were selected on media supplemented with geneticin (400 ppm) and screened for restoration of wild type phenotypes. The double knockout was amplified up- and downstream of MoYPEL1 with the primers 5F/5R-Gen and 3F-Gen/3R, respectively. A 1.8-kb G418 cassette was amplified with the primers Gen_F/Gen_R from pII99, which contains the geneticin gene. The double knockout mutant ΔΔMoypel1,2 was generated by co-transforming protoplasts of ΔMoypel2 with the deletion construct for MoYPEL1 and a geneticin cassette for selection.
Nucleic acid manipulation
Fungal genomic DNA was used for PCR and Southern blot hybridization. Genomic DNA was isolated using two different methods. Genomic DNA for general experiments including restriction enzyme digestion, agarose gel separation, and DNA gel blotting was isolated according to a standard method42. Genomic DNA was digested with a restriction enzyme, SacI, NcoI or SmaI, and blots were probed with a 500-base pair 5′ flanking cassette. DNA hybridization probes were labeled using Biotin-High Prime (Roche, Indianapolis, IN, USA) according to the manufacturer’s instructions. Chemiluminescent signal was detected using ChemiDoc XRS + system with Quantity One software (Bio-Rad Laboratories, Hercules, CA, USA).
Localization of MoYPEL:sGFP fusion proteins
The MoYPEL:sGFP fusion vectors were generated by overlap cloning. PCR products of 2.6 and 2.9 kb, which included the 2.0 kb of the 5′-flanking promoter region and the open reading frame region of the MoYPEL1 and MoYPEL2 genes, were amplified with the primers YPEL1_F/YPEL1_R and YPEL2_F/YPEL2_R (Supplementary Table S3), respectively, from wild type KJ201 genomic DNA. A total of 5.2 kb of the sGFP gene including the HPH gene was amplified with the primers pIG-YPEL1_F/pIG-YPEL1_R and pIG-YPEL2_F/pIG-YPEL2_R from pIGPAPA43. The YPEL PCR products containing the promoter region and the 5.2-kb region of pIGPAPA including the sGFP and HPH cassettes were cloned using the overlap DNA Cloning Kit (Elpis Biotech, Taejeon, Korea). Each MoYPEL:sGFP fusion vector was introduced into the transformant expressing the histone H1:RFP fusion protein by transformation27,28. Fluorescence microscopy images were captured with a Carl Zeiss Axio Image A2 microscope (Carl Zeiss Microscope Division, Oberkochen, Germany).
RNA isolation and expression analysis
For RT-PCR and qRT-PCR, total RNA was isolated from mycelia and conidia, respectively, using the Easy-Spin RNA extraction kit (iNtRON Biotechnology, Seongnam, Korea). First-strand complementary DNA (cDNA) was synthesized from total RNA using the SuperScript III First-strand Synthesis System (Invitrogen, Carlsbad, CA, USA) with oligo (dT) primers. RT-PCR was performed in a 20-μl reaction containing 10 ng of cDNA, 2.5 mM dNTPs, 2 μl of 10× PCR buffer, 1 μl (10 pmol) of each primer, and 1 unit of Taq polymerase. In all, 30 RT-PCR cycles were run on the Thermal Cycler Thermal Controller 2720 (Applied Biosystems, Foster City, CA, USA). The β-tubulin gene was included as a control. qRT-PCR reactions were performed as previously described44. The qRT-PCR mixture (final volume 10 μl) comprised 5 μl of Real-Time PCR 2× Master Mix (Elpis, Daejeon, Korea), 3 μl of forward and reverse primers (10 pmol of each), and 2 μl of cDNA template (25 ng μl−1). PCR was performed using a StepOne Real-Time PCR System (Applied Biosystems) as follows: 3 min at 95 °C (one cycle) followed by 15 s at 95 °C, 30 s at 60 °C, and 30 s at 72 °C (40 cycles). Primers for the transcript analyses of conidiation- and appressorium-related genes are listed in Table 1. To measure the relative abundance of each transcript, Ct values were normalized to those of β-tubulin (MGG_00604) and expressed as 2−ΔCt, where −ΔCt = (Ct, target gene − Ct, β-tubulin). Fold changes in expression during fungal conidiation were calculated as 2−ΔΔCt, where −ΔΔCt = (Ct, target gene − Ct, β-tubulin)conidiation − (Ct, WT − Ct, β-tubulin)conidiation45. qRT-PCR was performed with three independent pools of tissues in two sets of experimental replicates.
Developmental phenotype assays
Vegetative growth was measured on OMA, V8, and MM (3% sucrose, 0.2% NaNO3, 0.1% KH2PO4, 0.05% MgSO4∙7H2O, 0.05% KCl, 0.01% trace element, and 1.5% agar powder) 6 days after inoculation in six-well plates, with three replicates. To measure septum distance, hyphae on CM agar plates were stained with CFW to visualize septa and observed under a light microscope and under UV. The ability to produce conidia was measured by counting the number of conidia in 7-day-old V8 agar six-well plates. Conidia were collected by flooding the plate with 5 ml of sterilized distilled water. Conidia were counted using a hemocytometer under a microscope. Conidial germination and appressorium formation were measured on coverslips (Waldemar Knittel Glasbearbeitungs, Braunschweig, Germany). Harvested conidia were filtered through two layers of Miracloth (Calbiochem, La Jolla, CA, USA). Conidial suspensions (5 × 104 conidia ml−1) were placed on the hydrophobic side of the coverslips, placed in a moistened box, and incubated at 25 °C. After germination, conidia were measured. The percentage of germinated conidia forming appressoria was determined by microscopic examination of at least 100 conidia in three independent experiments and in triplicate.
Plant infection assays
For the spray infection assay, conidia were harvested from 8- to 10-day-old cultures on OMA plates. In total, 10 ml of conidial suspension (5 × 105 conidia ml−1) containing 250 ppm Tween 20 was sprayed onto 3-week-old plants of susceptible rice (cv. Nakdongbyoe). The inoculated plants were kept in a dew chamber at 25 °C for 24 h in the dark and moved to a growth chamber with a photoperiod of 16 h with fluorescent lights46. Disease severity was measured at 7 days after inoculation. Assays for appressorium penetration and invasive growth were performed using rice sheath tissues as described previously47. Briefly, conidial suspension (2 × 104 conidia ml−1) was dropped onto rice sheath tissue and incubated in a humid chamber at 25 °C. Invasive infection of hyphae was observed after 48 h by light microscopy.
References
Dean, R. et al. The top 10 fungal pathogens in molecular plant pathology. Mol. Plant Pathol. 13, 414–430 (2012).
Skamnioti, P. & Gurr, S. J. Against the grain: safeguarding rice from rice blast disease. Trends Biotechnol. 27, 141–150 (2009).
Talbot, N. J. On the trail of a cereal killer: exploring the biology of Magnaporthe grisea. Annu. Rev. Microbiol. 57, 177–202 (2003).
Lee, Y. H. & Dean, R. A. Hydrophobicity of contact surface induces appressorium formation in Magnaporthe grisea. FEMS Microbiol. Lett. 115, 71–75 (1994).
Li, G., Zhou, X. & Xu, J. R. Genetic control of infection-related development in Magnaporthe oryzae. Curr. Opin. Microbiol. 15, 678–684 (2012).
Li, Y., Zhang, X., Hu, S., Liu, H. & Xu, J. R. PKA activity is essential for relieving the suppression of hyphal growth and appressorium formation by MoSfl1 in Magnaporthe oryzae. PLoS Genet. 13, e1006954, https://doi.org/10.1371/journal.pgen.1006954 (2017).
Jiang, C., Zhang, X., Liu, H. & Xu, J. R. Mitogen-activated protein kinase signaling in plant pathogenic fungi. PLoS Pathog. 14, e1006875, https://doi.org/10.1371/journal.ppat.1006875 (2018).
Zhao, X., Kim, Y., Park, G. & Xu, J. R. A mitogen-activated protein kinase cascade regulating infection-related morphogenesis in Magnaporthe grisea. Plant cell 17, 1317–1329 (2005).
Thines, E., Weber, R. W. & Talbot, N. J. MAP kinase and protein kinase A–dependent mobilization of triacylglycerol and glycogen during appressorium turgor generation by Magnaporthe grisea. Plant cell 12, 1703–1718 (2000).
Xu, J. R., Staiger, C. J. & Hamer, J. E. Inactivation of the mitogen-activated protein kinase Mps1 from the rice blast fungus prevents penetration of host cells but allows activation of plant defense responses. Proc. Natl. Acad. Sci. USA 95, 12713–12718 (1998).
Jeon, J. et al. A putative MAP kinase kinase kinase, MCK1, is required for cell wall integrity and pathogenicity of the rice blast fungus, Magnaporthe oryzae. Mol. Plant Microbe. Interact. 21, 525–534 (2008).
Cools, T. & De Veylder, L. DNA stress checkpoint control and plant development. Curr. Opin. Plant Biol. 12, 23–28 (2009).
Kipreos, E. T. C. elegans cell cycles: invariance and stem cell divisions. Nat. Rev. Mol. Cell Biol. 6, 766–777 (2005).
Saunders, D. G., Aves, S. J. & Talbot, N. J. Cell cycle–mediated regulation of plant infection by the rice blast fungus. Plant cell 22, 497–507 (2010).
Veneault-Fourrey, C., Barooah, M., Egan, M., Wakley, G. & Talbot, N. J. Autophagic fungal cell death is necessary for infection by the rice blast fungus. Science 312, 580–583 (2006).
Osés-Ruiz, M., Sakulkoo, W., Littlejohn, G. R., Martin-Urdiroz, M. & Talbot, N. J. Two independent S-phase checkpoints regulate appressorium-mediated plant infection by the rice blast fungus Magnaporthe oryzae. Proc. Natl. Acad. Sci. USA 114, E237–E244 (2017).
Bardin, A. J. & Amon, A. Men and sin: what’s the difference? Nat. Rev. Mol. Cell Biol. 2, 815–826 (2001).
Palani, S., Meitinger, F., Boehm, M. E., Lehmann, W. D. & Pereira, G. Cdc14-dependent dephosphorylation of Inn1 contributes to Inn1–Cyk3 complex formation. J. Cell. Sci. 125, 3091–3096 (2012).
Li, C. et al. MoCDC14 is important for septation during conidiation and appressorium formation in Magnaporthe oryzae. Mol. Plant Pathol. in press; https://doi.org/10.1111/mpp.12523 (2016).
Roxström‐Lindquist, K. & Faye, I. The Drosophila gene Yippee reveals a novel family of putative zinc binding proteins highly conserved among eukaryotes. Insect Mol. Biol. 10, 77–86 (2001).
Hosono, K. et al. YPEL5 protein of the YPEL gene family is involved in the cell cycle progression by interacting with two distinct proteins RanBPM and RanBP10. Genomics 96, 102–111 (2010).
Hosono, K., Sasaki, T., Minoshima, S. & Shimizu, N. Identification and characterization of a novel gene family YPEL in a wide spectrum of eukaryotic species. Gene 340, 31–43 (2004).
Farlie, P. et al. Ypel1: a novel nuclear protein that induces an epithelial‐like morphology in fibroblasts. Genes Cells 6, 619–629 (2001).
Kelley, K. D. et al. YPEL3, a p53-regulated gene that induces cellular senescence. Cancer Res. 70, 3566–3575 (2010).
Liang, P. et al. MVP interacts with YPEL4 and inhibits YPEL4-mediated activities of the ERK signal pathway. Biochem. Cell Biol. 88, 445–450 (2010).
Lee, J. Y. et al. Pro-apoptotic role of the human YPEL5 gene identified by functional complementation of a yeast moh1Δ mutation. J. Microbiol. Biotechnol. 27, 633–643 (2017).
Jeon, J., Rho, H., Kim, S., Kim, K. S. & Lee, Y. H. Role of MoAND1-mediated nuclear positioning in morphogenesis and pathogenicity in the rice blast fungus, Magnaporthe oryzae. Fungal Genet. Biol. 69, 43–51 (2014).
Han, J. H., Lee, H. M., Shin, J. H., Lee, Y. H. & Kim, K. S. Role of the MoYAK1 protein kinase gene in Magnaporthe oryzae development and pathogenicity. Environ. Microbiol. 17, 4672–4689 (2015).
Liu, W. et al. Multiple plant surface signals are sensed by different mechanisms in the rice blast fungus for appressorium formation. PLoS Pathog. 7, e1001261, https://doi.org/10.1371/journal.ppat.1001261 (2011).
Geoghegan, I. A. & Gurr, S. J. Chitosan mediates germling adhesion in Magnaporthe oryzae and is required for surface sensing and germling morphogenesis. PLoS Pathog. 12, e1005703, https://doi.org/10.1371/journal.ppat.1005703 (2016).
Choi, J., Kim, K. S., Rho, H. S. & Lee, Y. H. Differential roles of the phospholipase C genes in fungal development and pathogenicity of Magnaporthe oryzae. Fungal Genet. Biol. 48, 445–455 (2011).
Rho, H. S., Jeon, J. & Lee, Y. H. Phospholipase C-mediated calcium signalling is required for fungal development and pathogenicity in Magnaporthe oryzae. Mol. Plant Pathol. 10, 337–346 (2009).
Parsons, K. A., Chumley, F. G. & Valent, B. Genetic transformation of the fungal pathogen responsible for rice blast disease. Proc. Natl. Acad. Sci. USA 84, 4161–4165 (1987).
Mulder, N. J. et al. InterPro, progress and status in 2005. Nucleic Acids Res. 33, D201–D205 (2005).
Kumar, S., Stecher, G. & Tamura, K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33, 1870–1874 (2016).
Yu, J. H. et al. Double-joint PCR: a PCR-based molecular tool for gene manipulations in filamentous fungi. Fungal Genet. Biol. 41, 973–981 (2004).
Choi, J., Kim, Y., Kim, S., Park, J. & Lee, Y. H. MoCRZ1, a gene encoding a calcineurin-responsive transcription factor, regulates fungal growth and pathogenicity of Magnaporthe oryzae. Fungal Genet. Biol. 46, 243–254 (2009).
Leung, H. et al. Transformation of the rice blast fungus Magnaporthe grisea to hygromycin B resistance. Curr. Genet. 17, 409–411 (1990).
Sweigard, J. A., Chumley, F. G. & Valent, B. Cloning and analysis of CUT1, a cutinase gene from Magnaporthe grisea. Mol. Gen. Genet. 232, 174–182 (1992).
Chi, M. H., Park, S. Y. & Lee, Y. H. A quick and safe method for fungal DNA extraction. Plant Pathol. J. 25, 108–111 (2009).
Yi, M. et al. The ER chaperone LHS1 is involved in asexual development and rice infection by the blast fungus Magnaporthe oryzae. Plant cell 21, 681–695 (2009).
Sambrook, J. & Russel, D. W. Molecular Cloning: A Laboratory Manual. 3rd ed. (Cold Spring Harbor Laboratory Press, 2001).
Horwitz, B. A. et al. A G protein alpha subunit from Cochliobolus heterostrophus involved in mating and appressorium formation. Fungal Genet. Biol. 26, 19–32 (1999).
Kim, K. S. & Lee, Y. H. Gene expression profiling during conidiation in the rice blast pathogen Magnaporthe oryzae. PLoS One 7, e43202, https://doi.org/10.1371/journal.pone.0043202 (2012).
Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔC T method. Methods 25, 402–408 (2001).
Park, J., Kong, S., Kim, S., Kang, S. & Lee, Y. H. Roles of forkhead-box transcription factors in controlling development, pathogenicity, and stress response in Magnaporthe oryzae. Plant Pathol. J. 30, 136–150 (2014).
Koga, H., Dohi, K., Nakayachi, O. & Mori, M. A novel inoculation method of Magnaporthe grisea for cytological observation of the infection process using intact leaf sheaths of rice plants. Physiol. Mol. Plant Pathol. 64, 67–72 (2004).
Kim, S. et al. Homeobox transcription factors are required for conidiation and appressorium development in the rice blast fungus Magnaporthe oryzae. PLoS Genet. 5, e1000757, https://doi.org/10.1371/journal.pgen.1000757 (2009).
Park, S. Y. et al. Global expression profiling of transcription factor genes provides new insights into pathogenicity and stress responses in the rice blast fungus. PLoS Pathog. 9, e1003350, https://doi.org/10.1371/journal.ppat.1003350 (2013).
Nishimura, M. et al. Mstu1, an APSES transcription factor, is required for appressorium-mediated infection in Magnaporthe grisea. Biosci. Biotechnol. Biochem. 73, 1779–1786 (2009).
Zhou, Z., Li, G., Lin, C. & He, C. Conidiophore stalk-less1 encodes a putative zinc-finger protein involved in the early stage of conidiation and mycelial infection in Magnaporthe oryzae. Mol. Plant Microbe Interact. 22, 402–410 (2009).
Lau, G. W. & Hamer, J. E. Acropetal: a genetic locus required for conidiophore architecture and pathogenicity in the rice blast fungus. Fungal Genet. Biol. 24, 228–239 (1998).
Madi, L., Ebbole, D. J., White, B. T. & Yanofsky, C. Mutants of Neurospora crassa that alter gene expression and conidia development. Proc. Natl. Acad. Sci. USA 91, 6226–6230 (1994).
Odenbach, D. et al. The transcription factor Con7p is a central regulator of infection‐related morphogenesis in the rice blast fungus Magnaporthe grisea. Mol. Microbiol. 64, 293–307 (2007).
Lee, B. N. & Adams, T. H. The Aspergillus nidulans fluG gene is required for production of an extracellular developmental signal and is related to prokaryotic glutamine synthetase I. Genes Dev. 8, 641–651 (1994).
Wieser, J., Lee, B. N., Fondon, J. W. & Adams, T. H. Genetic requirements for initiating asexual development in Aspergillus nidulans. Curr. Genet. 27, 62–69 (1994).
Matheis, S. et al. Functions of the Magnaporthe oryzae Flb3p and Flb4p transcription factors in the regulation of conidiation. Microbiol. Res. 196, 106–117 (2017).
Xu, J. R., Urban, M., Sweigard, J. A. & Hamer, J. E. The CPKA gene of Magnaporthe grisea is essential for appressorial penetration. Mol. Plant Microbe Interact. 10, 187–194 (1997).
Xu, J. R. & Hamer, J. E. MAP kinase and cAMP signaling regulate infection structure formation and pathogenic growth in the rice blast fungus Magnaporthe grisea. Genes Dev. 10, 2696–2706 (1996).
Choi, W. & Dean, R. A. The adenylate cyclase gene MAC1 of Magnaporthe grisea controls appressorium formation and other aspects of growth and development. Plant Cell 9, 1973–1983 (1997).
Acknowledgements
This study was supported by Basic Science Research Program through the National Research Foundation of Korea grant (NRF-2013R1A1A1008444) funded by the Ministry of Education, Science and Technology and by a grant from the Strategic Initiative for Microbiomes in Agriculture and Food, Ministry of Agriculture, Food and Rural Affairs, Republic of Korea (Grant no. 914009-04).
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J.-H.H. and J.-H.S. performed the experiments. J.-H.H. and K.S.K. contributed to analysis of data and writing of the manuscript. K.S.K. and Y.-H.L. conceived the experimental strategy and provided critical comments. All authors contributed to interpretation of the results followed by writing and/or reviewing the manuscript.
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Han, JH., Shin, JH., Lee, YH. et al. Distinct roles of the YPEL gene family in development and pathogenicity in the ascomycete fungus Magnaporthe oryzae. Sci Rep 8, 14461 (2018). https://doi.org/10.1038/s41598-018-32633-6
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DOI: https://doi.org/10.1038/s41598-018-32633-6
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