- Open Access
Spontaneous and CRISPR/Cas9-induced mutation of the osmosensor histidine kinase of the canola pathogen Leptosphaeria maculans
© The Author(s) 2017
- Received: 26 October 2017
- Accepted: 12 December 2017
- Published: 16 December 2017
The dicarboximide fungicide iprodione has been used to combat blackleg disease of canola (Brassica napus), caused by the fungus Leptosphaeria maculans. For example, in Australia the fungicide was used in the late 1990s but is no longer registered for use against blackleg disease, and therefore the impact of iprodione on L. maculans has not been investigated.
Resistance to iprodione emerged spontaneously under in vitro conditions at high frequency. A basis for this resistance was mutations in the hos1 gene that encodes a predicted osmosensing histidine kinase. While loss of the homologous histidine kinase in some fungi has deleterious effects on growth and pathogenicity, the L. maculans strains with the hos1 gene mutated had reduced growth under high salt conditions, but were still capable of causing lesions on B. napus. The relative ease to isolate mutants with resistance to iprodione provided a method to develop and then optimize a CRISPR/Cas9 system for gene disruptions in L. maculans, a species that until now has been particularly difficult to manipulate by targeted gene disruptions.
While iprodione is initially effective against L. maculans in vitro, resistance emerges easily and these strains are able to cause lesions on canola. This may explain the limited efficacy of iprodione in field conditions. Iprodione resistance, such as through mutations of genes like hos1, provides an effective direction for the optimization of gene disruption techniques.
- Agrobacterium-mediated transformation
- Gene editing
- HOG pathway
Canola (Brassica napus) is a major crop worldwide, and is also grown as part of the crop rotation systems with cereals . Control of the main disease of canola, blackleg, is through farming practices that minimize exposure to the infectious spores, sowing cultivars that carry resistance genes, and more recently relying on fungicides. Blackleg disease is caused by a species complex in the genus Leptosphaeria (Dothideomycetes; Pleosporales) [2–4], with most crop losses due to L. maculans. Although a number of molecular biology resources are available for L. maculans, including a genome sequence , investigations of gene functions in the fungus has been hampered by the low rates of homologous integration of constructs used in generating gene deletion strains, with just nine gene knock outs reported in the literature [6–11]. Hence, this aspect of the fungus has limited the ability to test how specific genes may impact the ability of this fungus to cause disease on canola.
The application of fungicides has provided large yield increases to crops by reducing the symptoms caused by fungal diseases. In the case of blackleg disease, different fungicides have been and continue to be employed . In Australia, currently these are in the triazole class [Fungicide Resistance Action Committee (FRAC) group 3], and used as seed dressings, combined with fertilizer, or as a foliar spray. In another class, the dicarboximide iprodione (FRAC group 2; trade name Rovral® produced by Bayer CropScience), was approved for use against blackleg disease and used for about 5 years before being unregistered at the end of the 1990s. Iprodione currently can still be used for treatment of Sclerotinia stem rot of canola, which is a disease that has an overlapping distribution as blackleg.
Resistance to dicarboximide fungicides, like iprodione, can occur if mutations arise in the high osmolarity glycerol response (HOG) pathway . The HOG pathway was first characterized in Saccharomyces cerevisiae for its role in enabling growth under hyper- and hypo-osmotic conditions [13–15], and subsequent research in numerous fungal species has defined multiple phenotypes of strains with mutations in the signaling genes. The HOG pathway features a sensing histidine kinase that transfers environmental information into a cascade of three mitogen activated protein kinases . Mutations often occur in the homologs of the histidine kinase in other fungi to confer resistance to the dicarboximide fungicides .
Exposure to fungicides is linked to the emergence of fungicide resistance, thereby rendering specific fungicides or entire classes ineffective. We recently initiated an investigation into the levels of resistance to triazole fungicides in L. maculans populations in Australia . As a control, isolates were tested for their responses against the unrelated chemical iprodione. Spontaneous resistance to this molecule was commonly observed, leading to the investigation into its basis and the impact of those mutations on pathogenicity. Subsequently, the hos1 gene that was mutated in these resistant strains was used as a tool for the development of the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system to make targeted mutations in L. maculans.
Fungal strains and culturing
Strains of Leptosphaeria spp. used in this study
L. biglobosa 06J154
Burren Junction, NSW, Australia, 2006 
D5 (IBCN18; M1)
Penshurst, VIC, Australia, 1988
Selection of D5 on iprodione
D5-IpR + hos1
hos1 − + hos1
Transformation of D5-IpR with wild type hos1
Streatham, VIC, Australia, 1988 
Selection of D2 on iprodione
D2-IpR + hos1
hos1 − + hos1
Transformation of D2-IpR with wild type hos1
Mt Barker, WA, Australia, 1988 
Selection of D3 on iprodione
D3-IpR + hos1
hos1 − + hos1
Transformation of D3-IpR with wild type hos1
Katanning, WA, Australia, 2014 
Selection of 14P290 on iprodione
14P290-IpR + hos1
hos1 − + hos1
Transformation of 14P290-IpR with wild type hos1
Cummins, SA, Australia, 2009 
hos1 guide; cas9
hos1 guide; cas9; hos1 −
cas9; hos1 guide
D13 cotranformed with both guide RNA (hyg) and Cas9 (G418)
cas9; hos1 guide; hos1 −
Selection of D13-CoT on iprodione
cas9; hos1 guide; hos1 −
Selection of D13-CoT on iprodione
In vitro crosses, France 
v23.1.3 transformed with pMAI23
cas9; AvrLm1 guide; avrLm1 −
cas9; AvrLm1 guide; avrLm1 −
For genetic segregation analysis, crosses were set up between strain D3-IpR and strain D13, on 20% V8 juice and CaCO3 medium. After 1 week of growth, the plates were overlaid with water agar. Cultures were incubated at 14 °C with alternating 12 h dark-blacklight cycles for 6 weeks. At this point, the plates were examined for the formation of pseudothecia. Asci were released by placing the pseudothecia in sterile water whereby ascospores were discharged naturally. Individual ascospores were then collected and allowed to germinate on 2% water agar plates before being hyphal-tip subcultured to create individual strains. A total of 28 progeny was collected and analyzed.
DNA isolation of L. maculans, PCR and sequencing
Leptosphaeria maculans mycelia were cultured in 10% cleared V8 juice medium (pH 6). Mycelia were freeze-dried, broken with 2 mm glass beads, and DNA extracted in a CTAB buffer and incubation at 65 °C, followed by one chloroform extraction, and precipitation with an equal volume of isopropanol .
For sequencing, hos1 was amplified with different primer combinations to cover different regions of this large gene. Amplicons used to identify spontaneous mutations were MAI0218-MAI0223 and MAI0220-MAI0224. Primer sequences used in this study are found in Additional file 1: Table S1. Primers used to amplify and then identify mutations in hos1 induced by CRISPR-Cas9 were MAI0220-MAI0224.
To resolve which hos1 allele is present in progeny of the D3-IpR × D13 cross, the region was amplified with primers MAI0220-MAI0376. The DNA was precipitated and then digested with AgeI restriction enzyme, which cuts the amplicon of the wild type copy but not the iprodione resistance allele.
Primers used to amplify the AvrLm1 gene to identify mutations induced by CRISPR-Cas9 were MAI0353-MAI0354.
Construction of plasmids for transformation of L. maculans
Plasmids were constructed for the introduction of T-DNA molecules into L. maculans using Agrobacterium tumefaciens mediated transformation.
Two plasmids conferring resistance to G418 or hygromycin were made, in which gene expression was from the promoter and terminator of the actin gene of L. biglobosa strain 06J154 . G418 resistance has not been used previously in L. maculans transformation. For the G418 construct, the promoter region was amplified with primers MAI0014-MAI0015, and terminator region with primers MAI0016-MAI0017 from genomic DNA of strain 06J154, isolated as for L. maculans. The open reading for the aminoglycoside phosphotransferase that confers resistance to G418 was amplified with primers ALID0835-ALID0836 from plasmid pPZP-NEO1 . The three pieces were joined by overlap PCR using primers MAI0014-MAI0017, and cloned into the TOPO pCR2.1 plasmid (Invitrogen). To ensure the expression system worked for resistance to G418, the equivalent plasmid was made to confer resistance to hygromycin. The promoter was amplified with primers MAI0018-MAI0024 and terminator with MAI0020-MAI0021. The hygromycin phosphotransferase gene was amplified with primers MAI0022-MAI0023 from plasmid pPZPHygHindX . The three pieces were joined together using primers MAI0018-MAI0021, and cloned into the TOPO 4.0 plasmid (Invitrogen). All PCRs used Platinum® Pfx DNA polymerase (Invitrogen). Plasmids containing clones without PCR-derived errors were identified, by sequencing the inserted fragments. The G418 resistance construct was excised with EcoRI and cloned into the EcoRI site of plasmid pPZP-201BK, which is able to replicate in Agrobacterium tumefaciens , to form pMAI2. The hygromycin resistance construct was excised with KpnI-SpeI and cloned into the KpnI-XbaI site of pPZP-201BK to form plasmid pMAI6.
Plasmid pLAU2 was constructed by cloning two fragments, the L. maculans actin (act1) promoter and the trp3 terminator, into pPZPHygHindX  digested with AscI and PacI using Gibson Assembly (New England Biolabs). Primers used to amplify the actin promoter, with Platinum® Pfx DNA Polymerase (Invitrogen), were AU1 and AU2 and for the trp3 terminator were AU5 and AU6. Primers were designed with additional nucleotides such that a BglII site was introduced between the promoter and terminator. Green fluorescent protein (GFP) was amplified with primers AU28 and AU31, and cloned into the BglII site of pLAU2 to form plasmid pLAU17. The act1 promoter and trp3 terminator combination was excised from plasmid pLAU2 using restriction enzymes SpeI and NheI and cloned into the XbaI site of plasmid pMAI2, to form pLAU53.
For complementation with the wild type copy of hos1, the gene was amplified with primers MAI0206 and MAI0207 using Q5 DNA polymerase (New England Biolabs) from genomic DNA of wild type isolate D5, and cloned using Gibson assembly (New England Biolabs) into plasmid pMAI2 that had been linearized with EcoRV and XhoI.
Constructs were made to express either the Cas9 endonuclease or the CRISPR guide RNAs using the actin promoter of L. maculans. Cas9 was amplified with primers MAI0225 and MAI0226 from plasmid pHSN401  and cloned into the BglII sites of pLAU2 and pLAU53 by Gibson assembly to form plasmids pMAI22 and pMAI23, respectively. The DNA fragment to target the endonuclease to hos1, guide RNA and two ribozymes were synthesized by Thermo Fisher Scientific (sequence in Additional file 2) and provided as a cloned product. The fragment was amplified using primers MAI0228 and MAI0229 and then inserted into the BglII sites of both plasmids pLAU2 and pLAU53 using Gibson assembly.
To streamline the production of the guide RNAs, two additional plasmids were made that incorporate the hepatitis delta virus (HDV) ribozyme, such that a single oligonucleotide of about 100 nt can be used for cloning the targeting RNA, rather than a synthesized and cloned DNA fragment. A XhoI restriction enzyme site was included to facilitate subsequent cloning of the gene-specific fragments. A DNA molecule (Additional file 2) was synthesized by Thermo Fisher Scientific, and amplified with primers MAI0228-MAI0229 and cloned into the BglII sites of both plasmids pLAU2 and pLAU53 using Gibson assembly to form plasmids pMAI75 and pMAI97, respectively.
A construct to produce a guide RNA to target mutations to the AvrLm1 gene was generated, by amplification off oligonucleotide MAI0336 with primers MAI0309-MAI0310, and cloning the amplicon into plasmid pMAI75 linearized with XhoI.
In all cases of plasmid construction that used amplification of DNA and subsequent cloning, the inserted DNA molecules in the plasmids were sequenced to either confirm that no PCR-induced errors occurred or to identify error-free clones.
Transformation of L. maculans with Agrobacterium tumefaciens
The plasmids were transformed into A. tumefaciens strain EHA105 using electroporation, and selected on LB medium + kanamycin (50 µg/ml). The Agrobacterium strains were then used to transform strains of L. maculans, with selection of fungal transformants using either G418 (100 µg/ml) or hygromycin (50 µg/ml), and cefotaxime (100–150 µg/ml) to inhibit Agrobacterium growth. The transformation of L. maculans was as follows. Overnight cultures of Agrobacterium in LB + kanamycin were diluted in sterile water and plated onto Agrobacterium induction medium  solidified with 2% agar (25 ml in 15 cm diameter Petri dishes) with pycnidiospores harvested in sterilized water from the L. maculans strains. Bacterial and fungal cells were spread across the plate. After 3 days incubation at 22 °C in darkness, 25 ml of cleared V8 juice 1.5% agar media containing selective antibiotics were overlaid. Transformed colonies emerged through the overlay agar 10–18 days later. The transformed strains were subcultured at least once onto V8 juice agar supplemented with the antibiotic suitable to select for fungal transformation and cefotaxime to inhibit Agrobacterium growth.
Quantification of antifungal drug resistance
Levels of resistance to two dicarboximide fungicides and a triazole fungicide were quantified in a radial growth assay, as in Ref.  with some modifications. In brief, for each strain 4 mm diameter mycelium plugs were inoculated into the center of 9-cm PDA petri dishes amended with a range of concentrations of technical grade iprodione (0.195–50 µg/ml), procymidone (0.195–50 µg/ml) and tebuconazole (0.0782–5 µg/ml) dissolved in dimethyl sulfoxide (DMSO). The colony diameter was measured in two perpendicular directions and values recorded in millimeters. EC50 values were calculated as described previously . EC50 values of wild type and complemented strains were analyzed by the Mann–Whitney U-test.
Spores of wild type and a GFP-expressing strain were germinated in cleared V8 juice (10%) and examined 3 days later using a Leica DM6000 microscope with an attached digital camera.
Plant inoculations and pathogenicity testing
Brassica napus cultivar Westar was grown in soil in growth cabinets. Two weeks after sowing the seed, pycnidiospore suspensions (106 spores/ml) from the L. maculans strains were placed as 10 µl drops onto wounded cotyledons. Lesions were scored on a 0–9 scale, as previously described , 11–14 days later.
Development of a positive selection system in L. maculans based on resistance to iprodione due to mutations in the hos1 gene
Wild type strains of L. maculans developed resistance to iprodione readily when mycelial plugs were inoculated on V8 juice agar medium supplemented with iprodione at concentrations up to 10 µg/ml. The fungicide at first inhibited growth, and then after several days a section of the mycelial plug initiated growth. These sectors were cultured and purified as single spore isolates.
Two methods were used to confirm that mutations in the hos1 gene caused the resistance to iprodione. The first approach was to analyze the segregation of traits and genotypes in progeny from a cross. Resistant strain D3-IpR was crossed with sensitive strain D13, and 28 progeny obtained. The strains were scored for growth on medium containing iprodione and genotyped for the hos1 allele by PCR–RFLP. The AgeI restriction enzyme recognition site (ACCGGT) of the wild type strain is lost in strain D3-IpR due to a base pair substitution (ACCCGT), as underlined. Nine progeny were sensitive to iprodione and 19 were resistant, which is not statistically different from the expected 1:1 ratio based on a χ2-test. The AgeI cut site polymorphism in hos1 co-segregated with the iprodione sensitive or resistant phenotype (Fig. 1b). The second approach was complementation of the mutant phenotype. A wild type copy of the hos1 gene was amplified and cloned into a plasmid that confers resistance to G418 for selection when the T-DNA is transformed into L. maculans. This construct was transformed into four strains that were iprodione resistant (i.e. D2-IpR, D3-IpR, D5-IpR and 14P290-IpR). Transformants were tested on medium containing iprodione. Reintroducing the wild type copy of hos1 into the strains caused them to become sensitive once again to iprodione, indicating that the mutations identified in hos1 were the cause of the resistance to this antifungal agent (Fig. 1c).
Half maximal effective concentration (EC50) measurements of fungicide action for strains of L. maculans
Iprodione EC50 (μg/ml)
Procymidone EC50 (μg/ml)
Tebuconazole EC50 (μg/ml)
P290-IpR + hos1
D2-IpR + hos1
D3-IpR + hos1
D5-IpR + hos1
Development of a CRISPR/Cas9 gene disruption system for L. maculans
Identification of gene functions in L. maculans through targeted gene replacements has been inefficient due to low rates of homologous integration of constructs. The potential to use a positive selection system, i.e. growth on iprodione when hos1 is mutated, was an impetus to use the hos1 gene for the development of gene targeting methods, specifically through CRISPR-Cas9.
A versatile pair of plasmids (pLAU2 and pLAU53) was created for strong constitutive transcription of DNA sequences that are cloned into them. Both plasmids feature the 1001 bp prior to the start codon (the promoter) of the act1 gene, encoding an actin subunit, and the terminator of trp3 encoding anthranilate synthase of L. maculans. Actin is considered to be constitutively expressed and is commonly used as the reference gene in quantitative reverse transcriptase PCR experiments [21, 28, 29]. The plasmid includes a BglII site between the promoter and terminator into which genes or other DNA fragments can be cloned. To test if this promoter and terminator combination was able to drive protein production, the open reading frame for GFP was cloned into plasmid pLAU2, and the T-DNA transformed into wild type L. maculans. Fluorescence was abundant in spores and hyphae of transformants, indicating that the construct induces gene expression and yields high and stable protein synthesis (Additional file 3: Fig. S1).
Iprodione resistant strains were cultured as mycelia, genomic DNA isolated, and the region spanning the site for CRISPR-Cas9 induced mutation in the hos1 gene amplified. Amplicons were digested with KpnI restriction enzyme and/or sequenced. All isolates derived from strains expressing both Cas9 and the hos1 RNA guide had mutations in this region (Fig. 4b). Most mutations were either the insertion of an additional nucleotide, or the deletion of one or several nucleotides (Fig. 4b). One strain, which is not illustrated in Fig. 4b due to the size of the DNA sequence, had a tandem duplication of 69 bp (acctggaaagacctcacggaaaacgtgaatggtatggccatgaatctcacaacccaggtgcgagaaatc). In all cases the mutations in hos1 were near the region of the genome where the guide RNA would target Cas9, indicating that they were derived from inaccurate repair of DNA damage by the endonuclease. The types of mutations also often differed from those found in the spontaneous mutants as many featured large deletions, compared to single nucleotide substitutions or insertions.
The pathogenicity of strains from one set of gene manipulations were tested by inoculating B. napus cotyledons. The three strains derived from the wild type produced lesions like the wild type isolate (Additional file 4: Fig. S2). This indicates that the introduction of Cas9 or a guide RNA into L. maculans does not impact its pathogenicity.
Improvements to mutation by CRISPR/Cas9
To eliminate the requirement to order synthesized DNA fragments, which have to be cloned due to the complexity in secondary structure (Thermo Fisher Scientific), two plasmids were created that have the regions for the HDV ribozyme and Cas9-binding RNA. This new plasmid system was then used to target the first Avr gene identified in L. maculans, AvrLm1. The hammerhead ribozyme and a region to target the AvrLm1 gene was synthesized as an 101 nucleotide oligonucleotide, amplified by PCR and cloned into the XhoI site of plasmid pMAI75. Cas9 was transformed into wild type strain v23.1.3, and then the guide RNA construct to mutate AvrLm1 was transformed into this strain. Genomic DNA isolated from the resulting transformants was used as the templates to amplify a fragment of AvrLm1, and amplicons then cut with NlaIII restriction enzyme. Two strains without the NlaIII site were obtained and AvrLm1 was amplified and sequenced from them. The mutant alleles had a single additional base pair or a 27 bp deletion (Additional file 5: Fig. S3). Thus, CRISPR-Cas9 can be used to isolate strains with mutations in genes, without a strong selection system as used for hos1.
Resistance to fungicides is a major problem in many areas of disease management, especially in agriculture with the high levels of antifungals applied to ensure maximum yield returns. For example, currently in Australia canola growers may apply triazole fungicides three times during a season, including as a seed dressing, in combination with fertilizer and as a foliar spray . Stubble is retained in the field after harvest, and the subsequent crop in the same field may receive fungicide treatments, thereby inadvertently causing additional exposure to the L. maculans populations while growing as a saprophyte in the canola stubble.
Resistance to iprodione and other dicarboximide fungicides and the underlying mechanisms have been well characterized in other plant pathogenic fungi, such as Botrytis cinerea [30–32]. The impact of mutation of hos1 in plant pathogens varies, in some cases impacting pathogenicity and in others having no effect . Hallmarks of impairing the HOG pathway, i.e. increased resistance to fludioxonil and sensitivity to salt, occur upon mutation of the hos1 gene in L. maculans, but the important ability to cause disease on plants is not. These results indicate that while iprodione is initially effective in vitro, resistance emerges easily, and these strains are still pathogenic on canola, potentially in part explaining the limited efficacy of iprodione in field conditions. Studies in other plant pathogenic fungi show differing results in terms of the contribution of the histidine kinase to pathogenicity. Similar to L. maculans, disruption of the gene does not impair pathogenicity in Alternaria alternata, Parastagonospora nodorum and Pyricularia oryzae [16, 33, 34]. In contrast, the homolog is required for pathogenicity in Botrytis cinerea, Fusarium oxysporum, Monilinia fructicola, Sclerotinia sclerotiorum and Ustilago maydis [35–39]. Deletion strains in Alternaria longipes form larger lesions on Nicotiana tabacum than the wild type . There is ambiguity about the role of the gene in A. brassicicola with isolates with point mutations having wild type pathogenicity, while a deletion allele, albeit analyzed in a large scale study, being less pathogenic [41, 42]. The histidine kinase contributes to the virulence of the human pathogens Candida albicans and Cryptococcus neoformans [43, 44].
Leptosphaeria maculans continues to be a recurrent disease of oilseed Brassicas around the world because the factors that this fungus produces to cause disease are mostly unknown. One challenge with finding new ways to combat L. maculans is that identifying gene functions has been technically challenging. Gene disruption in L. maculans is inefficient, with only nine genes disrupted as reported in the literature [6–11]. Constructs require large amounts of DNA for targeting by homologous recombination and even then the proportion of gene deletion events versus ectopic integration of the constructs is low, e.g. an efficiency of just one knock out from > 450 transformants screened . Advances in improving the proportion of targeted gene replacements versus ectopic integrations have been made, including the use of a counter selection system against ectopic insertion events  or using the selectable marker split into two pieces . However, isolating the large DNA fragments needed and/or the cloning into suitable vectors imposes limitations to the efficiency of created targeted mutations. For this reason, alternative methods to disrupt genes are needed for L. maculans, and the method employing CRISPR-Cas9 was explored.
CRISPR/Cas is a combination of an endonuclease that is guided to a specific site in a genome using an RNA molecule, found in Bacteria and Archaea for recognition of parasitic DNA elements and their specific cleavage. Modified for use in other organisms, its ability to make specific double-stranded breaks in DNA that are then inaccurately repaired to induce small mutations, such as within genes, is on the cusp of revolutionizing methods for gene functional studies, including in fungal species that have until now been difficult to manipulate genetically.
Here we used iprodione resistance due to mutation of the hos1 gene as an easy screening tool to develop CRISPR/Cas9 for L. maculans. Iprodione resistant strains derived from strains expressing Cas9 and a guide RNA targeting hos1 all had mutations at the place within hos1 where the endonuclease would cut the DNA. As proof-of-function that the method could work on other genes, the first avirulence gene that was identified in this fungus, AvrLm1, was disrupted . Targeting these effectors, all found to date to lie within distinctive large regions of AT-rich and highly repetitive DNA [5, 46], has not been possible using homologous recombination. Curiously, the avirulence profile of these strains did not change as predicted (data not shown), and will require additional experiments to understand what is emerging in L. maculans as complex multigene sets of interactions between fungal avirulence genes and plant resistance genes [46, 47].
In the first iteration of CRISPR/Cas9 for L. maculans, two rounds of transformation were used to separately introduce the guide RNA and Cas9 expression constructs into the fungus. After seeking a suitable promoter for regulation by RNA polymerase III in L. maculans without success, the dual ribozyme system to process the guide RNA when expressed from an RNA polymerase II promoter was used. This dual ribozyme approach was developed for plant transformation , and has recently also been employed in Aspergillus spp. , the basidiomycete human pathogen Cryptococcus neoformans  and the ascomycete plant pathogen Alternaria alternata . The disadvantage of using ribozymes for processing the guide RNA is that they add size to the constructs. To alleviate this issue, we created a vector such that just one of the ribozymes and the RNA fragment to target Cas9 to the gene to be mutated are synthesized: the hammerhead ribozyme requires folding with part of the target RNA and hence there is a requirement for long ~ 100 nucleotide oligonucleotides. The current method, although involving two transformation steps or co-transformation of both constructs, is suitable for making targeted mutations in genes, and has been tested in multiple wild type isolates. We have mutated more than 24 other genes in L. maculans to date (unpublished data). Potential refinements to the method in the near future will likely make it even more effective as a mutational tool to discover gene functions in L. maculans.
AI, DRV, and FJL-R conceived and designed the project. AI, ASU, DRV, SC, APVdW, and FJL-R designed and performed the experiments, and analyzed the results. AI wrote the manuscript. All authors read and approved the final manuscript.
We thank Edwin Lampugnani for providing the plasmid containing the Cas9 open reading frame.
The authors declare that they have no competing interests.
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All data generated or analyzed during this work are included in this article and its additional files.
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The research was supported by the Australian Grains Research and Development Corporation (Projects CUR00023 and UM00050, and Scholarship GRS11006) and the Australian Research Council (Grant FT130100146).
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