Plant resistance genes typically encode proteins with nucleotide binding site-leucine rich repeat (NLR) domains. Here we show that Ptr is an atypical resistance gene encoding a protein with four Armadillo repeats. Ptr is required for broad-spectrum blast resistance mediated by the NLR R gene Pi-ta and by the associated R gene Pi-ta2. Ptr is expressed constitutively and encodes two isoforms that are mainly localized in the cytoplasm. A two base pair deletion within the Ptr coding region in the fast neutron-generated mutant line M2354 creates a truncated protein, resulting in susceptibility to M. oryzae. Targeted mutation of Ptr in a resistant cultivar using CRISPR/Cas9 leads to blast susceptibility, further confirming its resistance function. The cloning of Ptr may aid in the development of broad spectrum blast resistant rice.
Plants have evolved a multifaceted, sophisticated defense response to microbial pathogens carrying effectors, as well as pathogen-associated molecular patterns (PAMP). The first tier of plant defense is PAMP-triggered immunity (PTI) mediated by pattern recognition receptors and occurs during pathogen attachment and the early phase of host-pathogen interactions. The second tier of plant defense is the effector-triggered immunity (ETI) mediated by plant resistance (R) genes, most of which encode cytoplasmic proteins with nucleotide binding site-leucine-rich repeat (NLR) domains1. In contrast to the structural conservation of most R proteins, effectors are highly diverse molecules with few conserved signatures. Despite the molecular diversity of pathogen effectors, plants have evolved various sophisticated mechanisms to detect intrusion of effectors and initiate robust disease resistance responses. A better understanding of these defense mechanisms will accelerate the translation of this knowledge into practical use in plant breeding and agriculture.
Rice is one of the most important foods for humanity and is widely consumed in the world. Blast disease of rice plants caused by the filamentous fungus Magnaporthe oryzae (synonymous with Pyricularia oryzae) is one of the most damaging diseases and frequently causes severe reduction of rice yield. The global annual crop loss due to blast was estimated at $66 billion and is enough to feed 60 million people2. Even without undergoing sexual reproduction, M. oryzae is capable of rapid genetic changes through active transposable elements, which can lead to a loss of avirulence (AVR) genes, resulting in the evasion of host defense and occurrence of rice blast disease3. So far over 100 major blast R genes have been identified and 30 of them have been molecularly cloned4. Major blast R genes, Pi-ta/Pi-ta2, Pi-z, Pi-b, and Pi-k/h/m/s, have also been deployed in some US rice varieties5. Nearly all of the cloned blast R genes encode NLR proteins that may directly or indirectly interact with fungal effectors to trigger ETI1. Noticeably, a cluster of blast R genes on rice chromosome 12 has been used to effectively reduce blast disease in indica germplasm worldwide since 1960. In the United States, the tropical japonica cultivar Katy has been widely used in breeding programs as a source of the Pi-ta resistance complex which includes three R genes, Pi-ta, Pi-ta2, and Ptr, in a region of suppressed recombination6,7,8. This complex was introgressed from the variety Tetep and has been shown to be effective in preventing infections by a wide range of M. oryzae strains in the US over two decades7,8. Compared to Pi-ta5, the Pi-ta2 gene confers higher levels of resistance, and it confers broader-spectrum resistance to all the same strains as Pi-ta plus additional strains9. Thus far, all rice varieties reported to contain Pi-ta2 also contain Pi-ta, and they are resistant to fungal strains with either AVR-Pita or another uncharacterized Pi-ta2-specific AVR gene9,10,11. The Ptr gene was identified in a fast neutron induced mutant (M2354) of Katy that still carries Pi-ta, but is susceptible to M. oryzae strains with AVR-Pita12. Subsequent analysis of a genetic cross between Katy and M2354 revealed a linked locus, Ptr, located in a linkage block near the centromere of Chromosome 12 and is presumably required for both Pi-ta and Pi-ta2 mediated disease resistance12.
Here we show that Ptr encodes two isoforms, each with four Armadillo (ARM) repeats. We find that a two base pair (bp) deletion within the Ptr protein coding region in the mutant line M2354 produces a truncated protein rendering susceptibility to M. oryzae. The resistance function of Ptr is further confirmed by showing that targeted mutation of Ptr in a resistant cultivar using CRISPR/Cas9 leads to blast susceptibility. More importantly, our genetic analysis suggests that Ptr, a non-NLR protein, functions in broad-spectrum blast resistance independent of Pi-ta, providing a strategy for developing blast resistance rice cultivars.
Molecular cloning of the Ptr gene
To clone the Ptr gene, a blast susceptible indica rice variety, Amane, containing Pi-ta was crossed with Katy (Pi-ta/Pi-ta2/Ptr). The Ptr gene was initially mapped to the short arm of chromosome 12 between microsatellite (SSR) markers RM3246 and RM1047 using 162 F2 individuals, and its resistance phenotype was confirmed in the F3 progenies by inoculating with blast race (isolate) IB-49 (ML1) (Fig. 1a). An additional 1456 F2 individuals were genotyped using RM3246, RM27941, and RM1047 to identify 105 recombinants. Four additional SSR markers, W137, W121, W195, and W249, were developed to screen the recombinants along with RM27946 delimiting the region between W249 and RM27946 (Fig. 1b). To fine map Ptr, an additional 10,000 F2 progeny of the Amane x Katy cross were evaluated to identify five recombinants with SSR marker W195 at one border and one recombinant with cleaved amplified polymorphic sequence (CAPS) marker Z14 at the other border (Fig. 1c, d). The insertion/deletion (InDel) marker Z12 at LOC_Os12g18729 was found to co-segregate with Ptr. A comparison of the corresponding genomic region of Ptr in Amane and Katy revealed 23 single nucleotide polymorphisms (SNPs) and four InDels that distinguish Katy from Amane. Among them, five SNPs resulting in nonsynonymous mutations and one 12 bp deletion resulting in a four- amino acid deletion defines the functional region of Ptr in the fourth exon (Supplementary Table 1).
Rice mutant M2354 carrying Pi-ta is susceptible to M. oryzae isolates with AVR-Pita12. DNA sequence alignments between M2354 and Katy of six candidate genes within the 63 kb mapping region revealed only a 2 bp (GG) deletion in the fourth exon of the LOC_Os12g18729 gene, creating a premature stop codon (Fig. 1e). To verify if susceptible ptr in M2354 is allelic to that of Amane, 800 F2 progeny from crossing Amane with M2354 were phenotyped and all were shown to be blast susceptible, suggesting that ptr in M2354 is allelic to ptr in Amane. To validate this finding, we analyzed 160 F3 progeny of the same cross with InDel markers developed from the 2 bp deletion in M2354 and 12 bp insertion in Amane. All F3 lines either heterozygous or homozygous at ptr were susceptible, verifying that ptr in Amane is allelic to ptr in M2354 (Supplementary Table 2).
To determine if the 2 bp deletion in M2354 resulted in a truncated protein that co-segregated with blast susceptibility, the InDel marker Z11, specific to the deletion in M2354, was used to analyze 300 F2:3 individuals of the cross between M2354 and Katy. The resulting data showed that all 81 susceptible individuals contain the 2 bp deletion, whereas all resistant individuals lack the deletion (Supplementary Table 2). Taken together these data strongly suggest that locus LOC_Os12g18729 is the Ptr gene.
Function validation of Ptr using CRISPR/Cas9
To confirm the function of Ptr, we examined whether disruption of Ptr in the resistant cultivar Katy would lead to the same susceptible phenotype as the M2354 mutant. Targeted mutation was performed at the LOC_Os12g18729 locus using CRISPR/Cas9. Two sequence-specific guide RNAs (gRNAs) were designed to disrupt the Ptr gene sequence in the third exon in front of the 2 bp mutation found in M2354 (Fig. 2a) ensuring that the targeted mutation will affect this region. The targeting sites encompassed an EcoNI (protospacer 1) and a SacI site (protospacer 2) to allow rapid evaluation of the mutation sites by PCR-restriction enzyme (PCR-RE) assay (Fig. 2a and Supplementary Fig. 1a). InDels generated by Cas9 typically lead to frame-shift mutations downstream of the targeted site and eventually result in the formation of a premature stop codon. A total of 34 plants from four independent events were obtained and confirmed to carry mostly InDels or a deletion of 810 bp between the two targeting sites (Fig. 2a and Supplementary Fig. 1b). Subsequently, the progeny derived from nine CRISPR-edited mutants (including plant 3H that carried two wild-type alleles and was not a true mutant) were inoculated with two avirulent races (isolate), IB-49 (ML1) or IC-17 (ZN57), of M. oryzae carrying AVR-Pita12. In comparison with Katy, CRISPR-edited ptr mutants exhibited a much larger lesion area and had a higher disease rating with both spray- and spot-inoculations (Fig. 2b–d and Supplementary Figs 2 and 3). Therefore, the targeted mutation of Ptr in the resistant Katy cultivar led to disease susceptibility to avirulent isolates, further confirming that Ptr is required for rice blast resistance.
Ptr function is independent of Pi-ta
The complete susceptibility of M2354 with the truncated ptr protein suggests Pi-ta requires Ptr to function (Supplementary Table 3). To examine if Pi-ta is required for Ptr function, we identified three Ptr-containing recombinant inbred lines (RILs), S/C272, S/C324, and S/C353, lacking Pi-ta and Pi-b from the cross of Saber with Cybonnet (Supplementary Table 4). Saber carries Pi-b and Pi-km but lacks Pi-ta/Pi-ta2/Ptr resistance alleles resulting in susceptibility to isolates carrying AVR-Pita. Cybonnet was bred from Katy carrying Pi-ta/Pi-ta2/Ptr. Inoculation of these RILs with fungal isolates lacking AVR-Pi-km excluded recognition by Pi-km13. As expected, S/C272, S/C324, and S/C353 were resistant to the fungal race/isolate IB-49 (ML1) with AVR-Pita (Fig. 3a). To verify that resistance in these RILs was associated with the Ptr gene, we crossed S/C272 with the blast susceptible rice variety M202 (lacking Pi-ta/Pi-ta2/Ptr) and tested progeny with the Ptr gene-specific marker Z12. As shown in Supplementary Table 5, resistance to IB-49 (ML1) co-segregated with the Ptr gene in F2 progeny suggesting that the Ptr gene-mediated resistance can be inherited. Taken together these data suggest that Ptr is a Pi-ta independent blast R gene.
Ptr is required for broad-spectrum resistance
To determine the resistance spectrum of Ptr relative to Pi-ta and Pi-ta2, 389 genetically diverse isolates14 collected from the United States were used to inoculate Katy and M2354. The extremely susceptible japonica rice cultivar Lijiangxintuanheigu (LTH) with an unknown R gene was resistant to only six of these isolates. In contrast, Katy carrying Pi-ta, Pi-ta2, Ptr, and Pi-ks was resistant to 348 isolates. Katy mutant M2354 with a truncated ptr gene, but still containing Pi-ta/Pi-ta2 and Pi-ks, was only resistant to 17 isolates. Therefore, Ptr plays a major role in the broad-spectrum resistance associated with the Pi-ta resistance complex12 (Supplementary Data 1).
To determine the resistance spectrum of rice lines with Ptr but without Pi-ta, we inoculated S/C272, S/C324, and S/C353 RILs with six Pi-km virulent blast races/isolates of IB-1 (15A6_3, 15L22_3), IB-17 (SSID116), IB-49 (ML1), IC-17 (ZN57), and IE-1 (14A15–2). As shown in Fig. 3a, resistance was observed for all six isolates. As a control, resistance was also observed when these RILs were inoculated with AVR-Pita-containing strains IE-1K (+AVR-Pita), a virulent strain that was transformed with the original reference AVR-Pita from blast strain O-13711,15. Rice varieties Pi No. 1 and YT14 that only contain Pi-ta showed moderate levels of resistance to two strains, IE-1K (+AVR-Pita) and IC-17 (ZN57), and rice varieties Nipponbare and YT16 that lack all three genes were susceptible to all strains (Fig. 3a). These data indicate that Ptr is required for a broader-spectrum of blast resistance than Pi-ta alone.
Relationship between Ptr and Pi-ta2
To determine the relationship between Ptr and Pi-ta2, differential rice varieties with Pi-ta2 and/or Pi-ta with or without various Ptr alleles were used for blast inoculations using differential blast races including a virulent race IE-1K (+AVR-Pita)11 (Fig. 3a, b). DNA sequence analysis showed that Ptr haplotypes in these rice varieties with Pi-ta2 are identical to that of Katy and rice varieties carrying only Pi-ta have a different ptr haplotype. Eight additional rice varieties known to contain Pi-ta2, including Pi No. 5 and IRBLta2_Re, share the Katy Ptr resistance allele containing the 12 bp deletion (Supplementary Table 6). The Pi-ta2/Ptr varieties Katy, Pi No. 5 and IRBLta2_Re show stronger, broader-spectrum resistance than varieties that contain only Pi-ta (Fig. 3a). Based on this data it is not possible to distinguish between Ptr and Pi-ta2.
To further define the resistance spectrum of Ptr, 10 differential varieties/lines were repeatedly inoculated with 18 diverse contemporary blast races/isolates (Table 1). Rice variety IR64 which contains the Pi-ta resistance complex plus additional blast R genes, was used as a resistant control6. LTH, the recurrent parent for IRBLta2_Re with Pi-ta2, and M202 were used as susceptible controls. The resistance frequencies of Pi-ta rice varieties YT14 and Pi No.1 were 27.8% and 38.9%, respectively. The resistance frequency of S/C272 with Ptr but without Pi-ta was 77.8%. The resistance frequency of Katy (88.9%) (Ptr/Pi-ta2 + Pi-ta) is identical to that of two diverse Pi-ta2-containing rice varieties, IRBLta2_Re and Pi No.5. Therefore, based on assays with diverse fungal strains, the Ptr resistance spectrum is highly similar to that of Pi-ta2.
We tested if mutation of Ptr impacted recognition of both AVR genes previously associated with Pi-ta2. Specifically, these are AVR-Pita and a second uncharacterized AVR gene identified by isogenic AVR strain/virulent mutant pairs16. Together with known Pi-ta and Pi-ta2 rice varieties, mutant M2354 with the truncated ptr gene was assayed for resistance to the diagnostic strain pairs for AVR-Pita and the second Pi-ta2 AVR gene (Supplementary Table 3). Mutation of Ptr compromises recognition and responses mediated by both Pi-ta2 associated AVR genes. Again, Ptr and Pi-ta2 are indistinguishable based on the data we have obtained so far.
Expression analysis of the Ptr and Pi-ta genes
The Ptr gene was expressed constitutively in all plant parts with transient induction within 16 h in both compatible (Amane) and incompatible (Katy) interactions (Supplementary Fig. 4a, b). Similarly, the Pi-ta gene was expressed constitutively in Katy and Amane with transient induction at 16 h in both compatible and incompatible interactions. In susceptible M2354, the highest transcript accumulation was at 24 h post-inoculation (hpi) for Pi-ta and at 48 hpi for ptr suggesting that both genes have roles during disease development (Supplementary Fig. 4b, c).
Subcellular location of the Ptr protein
The Ptr gene is located 211 kb away from Pi-ta and the genomic sequence of Ptr in Katy is 7713 bp. Comparison of cDNAs predicted two or three introns producing two putative proteins with 864 (A isoform) and 905 (B isoform) amino acids, respectively (Fig. 1f). Significant matches of an Armadillo (ARM) repeat domain without a U-box indicate Ptr may encode a non-typical E3 ligase (Fig. 1f). The absence of a nuclear localization signal in the Ptr protein suggests that Ptr may be localized in the cytoplasm of plant cells. To test this prediction, we made in-frame fusions of the coding regions of both Ptr isoforms (2592 bp and 2715 bp, without stop codon) with enhanced green fluorescent protein (EGFP) gene to produce Katy isoforms A and B: C-terminal EGFP fusion proteins for transfection into rice protoplasts. However, fluorescence signals from Katy A and B: C-terminal GFP were weakly visible (Supplementary Fig. 5). Consistently, the same fusion protein induced cell death in Nicotiana leaves via Agrobacterium-mediated expression, suggesting that this fusion protein is toxic to plant cells. Then, we made an in-frame fusion protein with a susceptible ptr protein from Amane. Subsequently, C-terminal GFP fusion proteins were produced from two ptr isoforms from Amane, namely, Amane A isoform (868 amino acids = Katy A isoform +4 amino acid insertion) and Amane B isoform (909 amino acids =Katy B isoform +4 amino acid insertion), as well as from the truncated ptr protein in M2354 (B isoform-645 amino acids). The resulting three constructs were transfected into rice protoplasts using the whole-cell-localized red fluorescent protein (RFP) as a control. The Amane-A fusion protein without the 41 N- terminal amino acids was localized in the whole cell, whereas the Amane-B fusion protein was mainly localized in the cytoplasm. In contrast, the truncated M2354:GFP fusion protein localized mainly in the nucleus (Fig. 1g), suggesting that proper cytoplasmic-nuclear localization of Ptr may be important for its resistance function.
Biochemical analysis of the Ptr protein
Ptr encodes the ARM repeat domain found in E3 ligases known to be involved in plant R gene-mediated resistance17. An ubiquitination assay was performed with Maltose Binding Protein (MBP) in-frame fused with the B isoform of the Ptr protein from Katy, Amane, and M2354, respectively. The fusion protein could not be expressed in bacteria. Fusion proteins of Ptr without a predicted transmembrane domain, 234 amino acids at N terminus, were made. As shown in Supplementary Fig. 6a, fusion proteins with expected sizes were purified for assays. Polyubiquitination occurred with positive control AvrPtoB, an E3 ligase protein as expected18; however, this event was not observed for Ptr from Katy despite E2 adducts being seen with and without Ptr (Supplementary Fig. 6b). To eliminate E2-ubiquitin adducts, we performed the same assays with a total of 10× dilutions of four different E2, one of which was shown in Supplementary Fig. 6c. The absences of polyubiquitination signals at the sites for the predicted Ptr proteins from Katy, M2354, and Amane (Supplementary Fig. 6d) suggest that Ptr is not an E3 ligase.
Natural variation at the Ptr locus
In the absence of E3 ligase activity, we reasoned that the structural integrity of the Ptr protein including the ARM repeat may be important for initiating defense responses. However, we identified five nonsynonymous substitutions and a 12 bp deletion in the fourth exon separating resistant Ptr in Katy and susceptible ptr in Amane outside of the ARM repeat domain. We then focused on this region of the Ptr gene (Supplementary Table 1). To validate the 12 bp deletion, we sequenced the fourth exon of Ptr in 13 resistant and 15 susceptible rice varieties (Supplementary Table 6). Noticeably, the 12 bp InDel and its two nearby nonsynonymous SNPs, resulting in a four amino acid deletion (KPEK) and amino acid alterations at M869K and E871K in resistant varieties, distinguish blast resistant from susceptible varieties (Supplementary Table 6). In contrast, the remaining SNP sites, existing in both resistant and susceptible varieties, do not distinguish their disease reactions. To rule out the presence of polymorphic sequences in other exons we sequenced coding regions of a few selected Ptr haplotypes (Table 2). Besides the deletion of four amino acids, nucleotides at positions 6925 and 6930 altered amino acids from M to K (at 869 aa sequence) and E to K (at 871 aa sequence), respectively, correlated with disease resistance specificity.
We noticed that most nucleotide variations are in the fourth exon of Ptr as indicated by significant Pi value (Fig. 4a,b and Table 2). To determine if this 12 bp InDel co-segregates with resistance, 400 F2:3 individuals resulting from the cross between Amane and Katy were analyzed with the InDel marker Z12. The presence of the 12 bp region was strictly associated with blast susceptibility, whereas the absence of the 12 bp was associated with blast resistance, suggesting that Z12 can be a useful marker for the Ptr gene and that amino acid composition in the fourth exon is likely important for Ptr-mediated disease resistance (Supplementary Table 2).
Distribution of the Ptr gene in rice germplasm worldwide
To deduce the distribution of Ptr, we analyzed Ptr in IRRI 3 K dataset containing sequencing data of 3000 rice genomes from 89 countries19,20 and identified 16 haplotypes including the one containing the deletion of 12 bp in the fourth exon found in 48 mostly indica rice varieties (Supplementary Table 7 and Supplementary Data 2). Most importantly, the ptr haplotypes containing the 12 bp were found in most rice varieties in the IRRI 3 K dataset, and a few wild rice relatives genotyped by the Oryza Map alignment project (OMAP)21 suggesting that the resistant Ptr haplotype has newly evolved through a 12 bp deletion with its adjacent two nonsynonymous SNP mutations resulting in changes of six amino acids in indica subspecies (Fig. 4c and Supplementary Fig. 8). These findings suggest that genomic variation surrounding these InDels determines pathogen signal recognition specificity (Table 2). To validate that the genomic region in the fourth exon determines recognition specificity, we analyzed 16 haplotypes identified in the 3 K dataset (Fig. 5). Sliding window analysis of nucleotide variation based on SNPs for each haplotype revealed that the fourth exon has the most significant DNA sequence variation (Fig. 5a). Phylogenetic analysis showed that all Pi-ta containing rice varieties belong to haplotypes 1, 6, 12, 15, and 16 and only haplotype 16 has the resistance allele of Ptr (Fig. 5b) suggesting that blast resistance in rice varieties harboring the haplotypes 1, 6, 12, and 15 could be impaired due to the absence of Ptr resistance.
Ptr is specifically involved in Pi-ta/Pi-ta2 resistance
Because Pi-ta requires the Ptr gene to be fully functional, the question was raised if Ptr may also be involved in other blast R gene-mediated disease resistance. Therefore, we examined if Ptr is involved in Pi9 mediated blast resistance. The monogenic line IRBL9-W carrying Pi9 was resistant to 14 M. oryzae races/isolates common to the US including IB-49 (ML1) and IC-17 (ZN57)22. We sequenced the Ptr allele in IRBL9-W and recurrent parent LTH. A single base deletion occurred before the 12 bp insertion in the fourth exon, resulting in a smaller ptr protein due to a frame-shift and suggesting that ptr in IRBL9-W did not compromise the Pi9 mediated blast resistance (Supplementary Fig. 8 and Supplementary Table 8). Similarly, we showed resistant monogenic lines, IRBLzt-T carrying Piz-t, IRBLkm-Ts carrying Pi-km, IRBLPi-kh-k3 carrying Pi-kh, and IRBLkp-K60 carrying Pi-kp, lack the Ptr gene as determined with the Ptr functional marker (Supplementary Table 8) suggesting that Ptr is not involved in Pizt and Pi-km/Pi-kh/Pi-kp mediated disease resistance. Previously, we demonstrated that Ptr is involved in both Pi-ta and Pi-ta2 (Supplementary Table 3), but not involved in Pi-ks mediated blast resistance as evidenced by an incompatible interaction to the AVR race IB54 in M235412. Taken together, we suggest that Ptr is specifically involved in Pi-ta/Pi-ta2 mediated blast resistance.
Ptr homologs in other plants
To determine how universal the Ptr gene is in plant species, we searched for Ptr homologs using protein BLAST program in NCBI database (https://blast.ncbi.nlm.nih.gov/Blast.cgi) and identified Ptr orthologs/homologs mainly in monocots including rice, Sorghum bicolor, Brachypodium distachyon, and Panicum hallii (Supplementary Figs 9 and 10). These findings suggest that there exists a unique defense system in monocots.
Rice varieties with the Pi-ta, Pi-ta2, and Ptr genes near the centromere region of chromosome 12 have been effective in reducing blast infection in the US for over two decades, suggesting the existence of an effective signal recognition and transduction mechanism to trigger rice immunity. In the present study, we fine mapped the Ptr gene within a 63 kb region nearby Pi-ta, and sequence analyses of all six candidate genes in a fast neutron induced susceptible mutant M2354 only identified a 2 bp deletion resulting in a truncated ptr protein. We validated the resistance function of the Ptr gene by demonstrating that 34 CRISPR/Cas9 knockout lines carrying different frame-shift mutations in the Ptr gene were blast susceptible versus the resistant wild-type parent.
A rice variety with Pi-ta2 reportedly confers a broad-spectrum blast resistance10, that was verified after the monogenic line IRBLta2-Pi carrying Pi-ta2 was inoculated with 14 commonly found US blast races22. In that study, Wang et al.22 demonstrated that the monogenic line IRBLta-K1 with Pi-ta was moderately resistant to one isolate of IC-17 (7.1%), whereas IRBLta-Pi with Pi-ta2 was resistant to the most of them (78.6%) suggesting that Pi-ta2 confers broader-spectrum of blast resistance compared to Pi-ta. Previously, we demonstrated that Katy also contains another blast R gene, Pi-ks, that confers avirulence to the race IB-54 in addition to Pi-ta that confers avirulence to isolates with AVR-Pita12. M2354 carrying Pi-ks and a defective ptr was extremely susceptible to over 300 diverse rice blast isolates (Supplementary Data 1). M2354 is a fast neutron induced near isogenic line of Katy examined by genome-wide SSR analysis, and no differences of morphological and agronomic traits were observed between Katy and M235412. We suggest that extreme blast susceptibility of mutant-M2354 is due to the loss of function of the Ptr gene in the resistant parent Katy. We then identified three S/C RILs with Ptr but without Pi-ta, and showed that they were resistant to more races/isolates, including that of Pi-ta. We demonstrated that Ptr is required not only for resistance mediated by Pi-ta, but also for a broader spectrum of blast resistance (Fig. 3; Table 2 and Supplementary Tables 3 and 8), though further evidence will be required to test if Ptr can confer this resistance independently. Additionally, we showed that a mutation in Ptr eliminates recognition of both AVR-Pita and the Pi-ta2-specific AVR gene associated with Pi-ta2 (Supplemental Table 3). We also showed that all examined rice varieties reportedly carrying Pi-ta2 contain the identical Ptr haplotype (Table 2, Fig. 4 and Supplementary Table 6). Ptr and Pi-ta2 are indistinguishable based on this data though further research will be required to determine if they are the same gene.
We found no evidence that the Ptr gene may be involved in resistance mediated by other blast R genes. The fact that Pi-ta can recognize isolates with AVR-Pita (in O-137)11,15, and Ptr can recognize isolates with AVR-Pita haplotypes in US M. oryzae strains12 suggests that plants have developed a fail-safe mechanism to activate ETI (Fig. 3 and Supplementary Fig. 11). Continued investigation of underlying molecular mechanisms will help genetic engineering for improved blast resistance. We showed that destruction of Ptr in M2354 completely abolished the resistance mediated by Pi-ta and Pi-ta212 (Supplementary Table 3 and Supplementary Data 1) suggesting that the integrity of the Ptr gene products are essential for transducing the pathogen signal. We attempted to address questions such as cellular location of R gene products and domains important for specificity of recognition. Despite that Ptr:GFP fusion protein was toxic to plant cells, we were able to demonstrate that differential localization occurred when two isomers of the susceptible ptr gene and the altered ptr gene product from M2354 were expressed suggesting that proper cytoplasmic and nuclear localization are important for their roles in signaling recognition and transduction.
We showed that the rice Ptr gene encodes an atypical resistance protein with an ARM repeat and that it is required for the function of a classical NLR resistance protein Pi-ta. An E3 ligase typified with both U-Box and ARM repeat domain has been shown to be involved in plant disease resistance17,23. ARM repeat proteins with diverse and fundamental functions have been found in many eukaryotes23. We speculated that Ptr with an ARM repeat domain and without a U-box could be a novel E3 ligase. However, we were unable to demonstrate E3 ligase activity in vitro suggesting that the Ptr protein is more likely involved in protein-protein interactions and least likely involved in protein degradation through ubiquitin pathway17. Noticeably, besides several other amino acid variations, there is a 3 bp deletion at the identical position as the 12 bp deletion in the Ptr allele of Oryza longistaminata (KN539074.1_FG004), which is one of six candidate genes for another broad-spectrum blast R gene named Pi57(t)24. A four amino acid deletion and nucleotides at positions 6925 and 6930 altering amino acids from M to K and E to K, respectively, were found to correlate with disease resistance specificity (Table 2 and Fig. 4a). We also found Katy Ptr type alleles with the deletion in the fourth exon in most of 48 rice varieties in the IRRI 3 K rice genome database (Supplementary Table 7 and Supplementary Data 2). Taken together, these data suggest that these 4 amino acid residues of the Ptr protein determine the specificity of pathogen recognition and transduction.
Plant breeders observed that many plant disease R genes are clustered within small genetic intervals. On rice chromosome 12, at least 19 blast R genes including Pi-ta and Pi-ta2/Ptr were mapped, and most of them are concentrated around the centromere region24. Rice cultivars with Ptr, some of them carrying Pi-ta2 or both Pi-ta and Pi-ta2, suggest that Pi-ta, Pi-ta2, and Ptr genes have been introgressed into modern rice varieties independently by classical plant breeding6,25. However, we only identified 48 out of 2167 rice germplasm lines with Ptr based on IRRI 3 K database, 682 of them contain Pi-ta suggesting that Ptr has not been widely deployed (Fig. 5 and Supplementary Table 7). Because Pi-ta is physically close to Ptr on a chromosomal region lacking recombination, DNA markers for Pi-ta26 or for Ptr developed in this study can be excellent tools for improving blast resistance via marker-assisted breeding strategy.
The fact that most R proteins share a common structure is beneficial for engineering novel resistance specificities. However, much deeper studies of underlying mechanisms will be required before such a promise can be fulfilled. To date, most of the cloned plant R genes encode NLR proteins that act directly or indirectly to detect the fungal effectors for triggering disease resistance1. There are a few reports of non-NLR genes including a recessive pi21 allele resulting in the loss of function of a proline-containing protein that confers durable blast resistance in rice27 and the RPW8 gene for broad-spectrum resistance to downy mildew in Arabidopsis28. Additionally, a kinase-START gene was shown to confer resistance to a devastating disease caused by the stripe rust fungus Puccinia striiformis29, and a putative ABC transporter gene has been reported responsible for resistance to multiple fungal diseases in wheat30.
In summary, the cloning and characterization of Ptr reveals an atypical R protein. The discovery that a non-NLR gene Ptr is required together with an NLR gene Pi-ta for resistance to a wide range of blast isolates suggests that plants have evolved multifaceted mechanisms to cope with the rapid adaptation of plant pathogens31 (Supplementary Fig. 11). Stacking Ptr along with Pi-ta or other blast R genes near the centromere region of chromosome 12 may enhance the durability of rice disease resistance.
Plant materials and mapping populations used
Plant materials used in this study were mainly from the USDA National Plant Germplasm System (https://www.ars-grin.gov/npgs/). They are listed in Supplementary Table 9. Mapping populations used are: 1) An F2 population consisting of 11,618 individuals of the cross of the blast susceptible indica rice variety ‘Amane’ (PI 373335) from Sri Lanka with Pi-ta32 with the resistant tropical japonica variety ‘Katy’ with Pi-ta/Pi-ta2/Ptr (PI 527707); 2) An F2:3 population consisting of 300 individuals of the cross of a fast neutron induced Katy mutant M2354 with Pi-ta/Pi-ta2 with Katy11; and 3) An F2:3 population consisting of 800 individuals of the cross of M2354 with Amane.
Fungal material and disease evaluation
M. oryzae isolates used in this study were listed in the Supplementary Table 3 and Supplementary Data 1 and as indicated in Fig. 314. Rice plants were grown in a greenhouse. Briefly, the germinated rice seeds were sowed in a black plastic insert (2.9 × 4.0 × 5.6 cm3) with sterilized local silt loam soils from the field. A tray containing 96 of these inserts was filled with water, which was then diffused into seedling via open holes at the bottom. The seedlings were grown in the greenhouse at 24 to 30 °C with an 8h dark and 16h light cycle until V3 to V4 stages33 and placed in a large black plastic bag for inoculation with a spore suspension of M. oryzae. Race (isolate) IB-49 (ML1) carrying AVR-Pita111 was used to evaluate disease reactions of mapping populations. IB-49 (ML1) and IC-17 (ZN57) were used to inoculate CRISPR/Cas9 generated M2 plants. Spore production, suspension, inoculation, and evaluation were performed as described by Wang et al.32. Briefly, M. oryzae isolates were grown on oatmeal agar plates (BD Difco, NJ, USA) for 7 days at 21 to 24 °C under dark and white fluorescent light and were washed with 0.25% gelatin solution. Plants at 3- to 4- leaf stages33 were inoculated with 20 mL of the filtered spore suspensions (1 × 105 spores/mL) with an airbrush and placed inside a sealed black plastic bag for 24 h at 21 to 24 °C. Then, inoculated plants were moved out from the bags and transferred to the cooling room with an 8h light and 16h dark cycle with 80% relative humidity for additional 6 days. Disease reactions were determined on the second youngest leaf, using a categorical rating system from 0 (resistant) to 5 (susceptible), in which 0 = no visible lesion, 1 = a few small point lesions, 2 = lesion size smaller than 2 mm without obvious fungal mass, 3 = 10% of leaf area with lesions bigger than 2 mm, 4 = > 10% and <50% of the leaf with lesions bigger than 3 mm, and 5 = > 50% of leaf area with lesions >3 mm34. The disease reactions were repeated three times and its mean value was used for analysis.
Mapping and cloning of the Ptr gene
To map the Ptr gene, a bulk segregant analysis (BSA) was carried out using resistant (R) and susceptible (S) DNA pools, including 20 homozygous or heterozygous R and 20 homozygous S of the F2 derived from the cross of Amane with Katy, and phenotypes were confirmed in the F3 generation, respectively35. A total of 225 SSR markers distributing evenly on all 12 rice chromosomes were used to screen polymorphisms between R and S pools, and both parents. Five polymorphic SSR markers distinguishing R and S pools were identified. Linkage analysis was carried out using 162 individuals of F2 of the cross of Amane and Katy and the co-segregating and flanking markers in Fig. 1a were identified. To fine map Ptr, more SSR markers were developed or identified from the Gramene Markers Database (http://archive.gramene.org/markers/microsat/); InDel and CAPS markers were designed based on DNA variation within flanking markers in Fig. 1a between the japonica Nipponbare (http://rice.plantbiology.msu.edu/) and the indica IR64 (http://schatzlab.cshl.edu/data/rice/). Additionally, partial genomic sequences of the Ptr region of Katy and Amane were determined to identify more polymorphic markers. At the same time, an additional F2 population of 10,000 individuals was used to identify more recombinants because of a linkage block36. To identify the Ptr candidate gene, the genomic DNA fragments of all annotated genes predicted by MSU version 7.0 (http://rice.plantbiology.msu.edu/) between Katy and M2354 in the Ptr region were sequenced and analyzed. Additionally, the Ptr candidate gene in Amane and Pi-ta, Pi-ta2 differential rice varieties were also sequenced. All PCR primers and markers were designed using Primer Premier 5 software and were listed in the Supplementary Table 10.
RNA isolation and quantitative RT-PCR
Total RNA was extracted from various rice tissues using the RNeasy Plant Mini Kit (Qiagen, MD, USA) and treated with RNase-Free DNase (Qiagen). First-strand cDNA was synthesized using a PrimerScript II 1st Strand cDNA Synthesis Kit (Takara, CA, USA) with an oligo(dT) 18 primer according to the manufacture’s protocol. The qRT-PCR amplification was performed using SYBR® Premix Ex TaqTM II (Takara) with Roche LightCycler® 96 System (CT, USA) following the manufacturer’s instruction. The qRT-PCR amplification was performed with three biological replicates, and the rice Actin1 gene (LOC_Os03g50885) was used as an internal control for gene expression37.
Subcellular localization assays
To determine subcellular localization of Ptr, two predicted Ptr isoforms, A and B, corresponding to the entire protein coding region (2592 bp and 2715 bp, without stop codon) were amplified from cDNA of seedling leaves of Katy, Amane, and M2354, and cloned into EcoRI and SalI sites of the pYBA1132 vector to generate Ptr:EGFP, respectively. The fusion construct was transformed or co-transformed into rice protoplasts prepared from Nipponbare seedlings and Nicotiana using PEG-mediated or Agrobacterium-mediated methods as described38. The transformed protoplast cells were examined by a confocal laser-scanning microscope. The primers for localization study were listed in the Supplementary Table 11, and plasmid constructs were listed in the Supplementary Table 12.
Targeted mutagenesis of Ptr in rice with CRISPR/Cas9
The Ptr gene in the Katy cultivar was targeted with two gRNA spacers that span 811 bp in the third exon of the gene. The highly specific gRNA spacer sequences (Supplementary Table 13) were designed using the CRISPR-plant database and website39. The corresponding spacer sequences were fused with transfer RNAs (tRNAs) using the golden gate assembly method40. The resulting polycistronic tRNA-gRNA gene was then introduced into pRGEB32 (Addgene #63142) by digesting the gene with FokI and the plasmid with BsaI to release compatible overhangs before ligation with T4 Ligase (New England Biolabs, MA, USA). The resulting binary vector (pKO-Ptr) was introduced via electroporation into the Agrobacterium tumefaciens strain EHA105. Rice calli derived from mature seeds of the cultivar Katy were transformed with pKO-Ptr using the standard protocol40. The transformation events were selected based on hygromycin B resistance and the regenerated plants were analyzed for genome-edited mutations in the target gene. Chromosomal deletions were detected by PCR with primers flanking the two target sites of each gene. InDels on the target sites with RE sites were detected by PCR-RE assay after PCR products encompassing the target were digested with the appropriate RE for 2 to 3 h. Selected PCR products from the transgenic CRISPR-edited lines were sequenced to determine the specific mutation. Double peaks were resolved with degenerate sequence decoding method41. The primers for CRISPR/Cas9 study were listed in the Supplementary Table 13.
M. oryzae evaluation of CRISPR-edited transgenics
M. oryzae isolates IC-17 (ZN57) and IB-49 (ML1) were placed onto oatmeal agar (BD) plates and left to grow under constant white and UV light for eight to 9 days. Fungal spores from the agar were filtered with cheesecloth and collected into a 50 mL conical tube. Spore suspensions were measured with a hemocytometer and adjusted to a concentration of 1 × 105 spores/mL for both the spray- and spot-inoculations. Two-week-old wild-type plants and mutant lines were spray-inoculated with spore suspension using an air brush via a diaphragm compressor (Whirlwind II Model 80–2, Badger Air-Brush Co., IL, USA). Inoculated plants were placed into 30”x12”x18” plastic bins containing 2 in of water to act as a dew chamber. After 24 h plants were removed from the plastic bins and placed in an environmental chamber at 28 °C for five additional days. Disease susceptibility or resistance was evaluated based on blast disease rating and lesion development as previously described in an earlier methods section (Fungal material and disease evaluation). Blast symptoms were imaged using a Nikon camera with 60 mm f/2.8D AF Micro-Nikon lens. Image J and Microsoft Excel were used to analyze data and generate graphs. For spot-inoculation, rice leaves from two- and four-week-old wild-type plants and mutant lines were cut and placed into plastic containers containing filter paper and water to maintain a moist environment for disease development. Twelve leaves were inoculated and tested for wild-type and each mutant line. After inoculation of two spots on each leaf with 10 uL of spore suspension, leaves were incubated at room temperature (22 °C) for 6 days. Blast symptoms were recorded with photography and analyzed with ImageJ software to calculate the lesion area.
The entire coding region with 905 amino acids and partial coding sequence with 671 amino acids without predictive transmembrane domain of the N terminus of Ptr was cloned into SalI and EcoRI sites of the pMAL-c5X vector (NEB) to generate in-frame fusion proteins, respectively. The proteins were expressed at 20 °C and purified using amylose attached magnetic beads with an affinity for MBP fusion proteins according to the manufacturer’s protocol (NEB). In vivo ubiquitination was performed as described42. To detect ubiquitination, the products were run through stain-free SDS-PAGE gels (Bio-Rad) and transferred onto Nitrocellulose membranes (Thermo Fisher Scientific, NC, USA). The membranes were blotted with anti-ubiquitin (Boston Biochem, MA, USA) and anti-MBP (NEB), respectively. The images were detected using ChemiDoc Imaging System (Bio-Rad, CA, USA). The primers and plasmid constructs for the ubiquitination assay study are listed in the Supplementary Tables 11 and 12, respectively.
DNA sequence analysis
Because all functional polymorphism sites were identified in the fourth exon between Amane and Katy, we sequenced this exon to predict the origin and evolution of the Ptr gene. The fourth exon of the Ptr DNA sequences in various rice varieties was amplified using specific primers listed in the Supplementary Table 10. After gel purification, the DNA samples were sequenced at USDA-ARS Genomics and Bioinformatics Research Unit (Stoneville, Mississippi). The Ptr DNA sequences in O. barthii (OBART12G08790), O. glaberrima (ORGLA12G0083200), O. meridionalis (OMERI12G06260), O. longistaminata (KN539074.1_FG004), O. rufipogon (ORUFI12G09760), and O. nivara (ONIVA12G08670) were retrieved from the Oryza Map Alignment Project (OMAP)21 project on the Gramene website (http://www.gramene.org/). The DNA sequences were assembled using Vector NTI software and aligned with BioEdit version 7.2.5. A phylogenetic tree was constructed by the software MEGA 7.0. To determine the average number of nucleotide differences per site (Pi value) in Ptr, the entire coding region sequences of Ptr in Katy, YT14, YT16, Amane, Pi No.1, Pi No. 4, and BHA were used to build the sliding window with DNasp v5.
Ptr haplotype analysis in IRRI 3 K sequenced rice germplasm
To investigate the distribution of the resistant Ptr allele observed in Katy, we characterized haplotypes in the IRRI 3 K SNP Seek database19,20. The SNP data were extracted for the Ptr gene (LOC_Os12g18729) from the 4.8 M SNP database and haplotypes were characterized using 173 polymorphic sites within the exon regions of the gene. Data were obtained for 3,024 lines and lines that had missing data at SNP 10,833,409 were excluded, this SNP was correlated to the SNP InDel in sequence data presented in Supplementary Table 1. Lines with over 15% total missing data, with heterozygous alleles considered as missing, were excluded. Upon filtering, 2215 lines remained for haplotype characterization. Haplotypes were defined by having no SNP polymorphisms among lines in the same haplotype group. A total of 35 lines contained rare haplotypes (<10 lines within haplotype group) and these haplotype groups were not considered, and 13 lines were not able to be assigned to a haplotype group due to missing data. A total of 2167 lines were assigned to a haplotype group. The association of Ptr haplotypes to Pi-ta was conducted by comparing the functional Pi-ta SNP at 10,607,554 with the assigned Ptr haplotype group. Based on the sequence data, there appeared to be a single SNP difference between the haplotype groups that contained ‘Katy’ and ‘Drew’. These groups were not treated as separate haplotypes as it is known from pedigree that ‘Drew’ and ‘Katy’ contain the same allele through decent, as ‘Katy’ is the parent of ‘Drew’. SNPs of each Ptr haplotype of IRRI 3 K rice varieties in the coding regions were used to build the sliding window with DNasp v5 and a phylogenetic tree that was constructed with the software MEGA 7.0. See additional resource for varieties in each haplotype and predicted disease reaction and details of SNPs.
The full genomic sequence of the Ptr gene from Katy and Amane can be retrieved in GenBank (accession number: MG385185 and MG385186) (https://www.ncbi.nlm.nih.gov/search/?term=MG+385185). The coding region of rice varieties for sliding window in Fig. 5b can be retrieved from GenBank (accession number: MG385187 to MG385192) ((https://www.ncbi.nlm.nih.gov/search/?term=MG+385187). The fourth exon sequences for Fig. 5c can be retired from GenBank accession number: MG397008-MG397034 (https://www.ncbi.nlm.nih.gov/search/?term=MG+397008). The authors declare that all other data supporting the findings of this study are available within the manuscript and its supplementary files or are available from the corresponding author upon request.
Dangl, J. L., Horvath, D. M. & Staskawicz, B. J. Pivoting the plant immune system from dissection to deployment. Science 341, 746–751 (2013).
Pennisi, E. Armed and dangerous. Science 327, 804–805 (2010).
Dean, R. A. et al. The genome sequence of the rice blast fungus Magnaporthe grisea. Nature 434, 980–986 (2005).
Wang, B. H., Ebbole, D. J. & Wang, Z. H. The arms race between Magnaporthe oryzae and rice: Diversity and interaction of Avr and R genes. J. Integr. Agric. 16, 2746–2760 (2017).
Fjellstrom, R. et al. Development of DNA markers suitable for marker assisted selection of three Pi- genes conferring resistance to multiple Pyricularia grisea pathotypes. Crop. Sci. 44, 1790–1798 (2004).
Jia, Y. Artificial introgression of a large chromosome fragment around the rice blast resistance gene Pi-ta in backcross progeny and several elite rice cultivars. Heredity 103, 355–356 (2009).
Moldenhauer, K. A. K. et al. Registration of ‘Katy’ Rice. Crop. Sci. 30, 747–748 (1990).
Jia, Y. et al. Rice Pi-ta gene confers resistance to the major pathotypes of the rice blast fungus in the United States. Phytopathology 94, 296–301 (2004).
Kiyosawa, S. Gene analysis of blast resistance in exotic varieties of rice. Jpn. Agric. Res. Q. 6, 8–15 (1971).
Kiyosawa, S. et al. An attempt of classification of world’s rice varieties based on reaction pattern to blast fungus strains. Bull. Natl Inst. Agrobiol. Resour. 2, 13–39 (1986).
Orbach, M. J. et al. A telomeric avirulence gene determines efficacy for the rice blast resistance gene. Plant. Cell. 12, 2019-2032 (2000).
Jia, Y. & Martin, R. Identification of a new locus, Ptr(t), required for rice blast resistance gene Pi-ta-mediated resistance. Mol. Plant. Microbe Interact. 21, 396–403 (2008).
Ashikawa, I. et al. Two adjacent nucleotide-binding site-leucine-rich repeat class genes are required to confer Pikm-specific rice blast resistance. Genetics 180, 2267–2276 (2008).
Wang, X. et al. Dynamic changes in the rice blast population in the united states over six decades. Mol. Plant. Microbe Interact. 30, 803–812 (2017).
Dai, Y., Winston, E., Correll, J. C. & Jia, Y. Induction of avirulence by AVR-Pita1 in virulent U.S. field isolates of Magnaporthe oryzae. Crop J. 2, 1–9 (2014).
Bryan, G. T. et al. A single amino acid difference distinguishes resistant and susceptible alleles of the rice blast resistance gene Pi-ta. Plant Cell 12, 2033–2045 (2000).
Ning, Y. et al. A layered defense strategy mediated by rice E3 ubiquitin ligases against diverse pathogens. Mol. Plant 9, 1096–1098 (2016).
Zeng, L. et al. A tomato LysM receptor-like kinase promotes immunity and its kinase activity is inhibited by AvrPtoB. Plant J. 69, 92–103 (2012).
Mansueto, L. et al. Rice SNP-seek database update: new SNPs, indels, and queries. Nucleic Acids Res. 45, D1075–D1081 (2017).
Sun, C. et al. RPAN: rice pan-genome browser for ∼3000 rice genomes. Nucleic Acids Res. 45, 597–605 (2017).
Kim, H. et al. Construction, alignment and analysis of twelve framework physical maps that represent the ten genome types of the genus Oryza. Genome Biol. 9, R45 (2008).
Wang, J. C., Correll, J. C. & Jia, Y. Characterization of rice blast resistance genes in rice germplasm with monogenic lines and pathogenicity assays. Crop. Prot. 72, 132–138 (2015).
Peifer, M., Berg, S. & Reynolds, A. B. A repeating amino acid motif shared by proteins with diverse cellular roles. Cell 76, 789–791 (1994).
Dong, L. et al. Fine mapping of Pi57(t) conferring broad spectrum resistance against Magnaporthe oryzae in introgression line IL-E1454 derived from Oryza longistaminata. PLoS ONE 12, e0186201 (2017).
Rybka, K. et al. High resolution mapping of the indica-derived rice blast resistance genes II. Pi-ta2 and Pi-ta and a consideration of their origin. Mol. Plant. Microbe Interact. 10, 517–524 (1997).
Jia, Y., Wang, Z. & Singh, P. Development of dominant rice blast Pi-ta resistance gene markers. Crop. Sci. 42, 2145–2149 (2002).
Fukuoka, S. et al. Loss of function of a proline-containing protein confers durable disease resistance in rice. Science 323, 998–1001 (2009).
Xiao, S. et al. Broad-spectrum mildew resistance in Arabidopsis thaliana mediated by RPW8S. Science 291, 118–120 (2000).
Fu, D. et al. A kinase-START gene confers temperature-dependent resistance to wheat stripe rust. Science 323, 1357–1360 (2009).
Krattinger, S. G. et al. A putative ABC transporter confers durable resistance to multiple fungal pathogens in wheat. Science 323, 1360–1363 (2009).
Jia, Y. et al. Direct interaction of resistance gene and avirulence gene products confers rice blast resistance. EMBO J. 19, 4004–4014 (2000).
Wang, X. et al. Characterization of Pi-ta blast resistance gene in an international rice core collection. Plant Breed 129, 491–495 (2010).
Counce, P. A., Keisling, T. C. & Mitchell, A. J. A uniform, objective, and adaptive system for expressing rice development. Crop. Sci. 40, 436–443 (2000).
Wang, X. et al. Genome-wide association of rice blast disease resistance and yield-related components of rice. Mol. Plant. Microbe Interact. 28, 1383–1392 (2015).
Michelmore, R. W., Paran, I. & Kesseli, R. V. Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations. Pro. Natl Acad. Sci. USA 88, 9828–9832 (1991).
Jia, Y., Jia, M. H., Wang, X. & Liu, G. Indica and japonica crosses resulting in linkage block and recombination suppression on rice chromosome 12. PLoS ONE 7, e43066 (2012).
Zhao, H. et al. Disruption of OsSULTR3;3 reduces phytate and phosphorus concentrations and alters the metabolite profile in rice grains. New Phytol. 211, 926–939 (2016).
Liu, J. et al. The RhoGAP SPIN6 associates with SPL11 and OsRac1 and negatively regulates programmed cell death and innate immunity in rice. PLoS Pathog. 11, e1004629 (2015).
Xie, K., Minkenberg, B. & Yang, Y. Boosting CRISPR/Cas9 multiplex editing capability with the endogenous tRNA-processing system. Pro. Natl Acad. Sci. USA 112, 3570–3575 (2015).
Xie, K., Zhang, J. & Yang, Y. Genome-wide prediction of highly specific guide RNA spacers for CRISPR-Cas9-mediated genome editing in model plants and major crops. Mol. Plant 7, 923–926 (2014).
Ma, X. et al. Rapid decoding of sequence-specific nuclease-induced heterozygous and biallelic mutations by direct sequencing of PCR products. Mol. Plant 8, 1285–1287 (2015).
Zhou, B. et al. A subset of ubiquitin-conjugating enzymes are essential for plant immunity. Plant Physiol. 173, 1371–1390 (2017).
Li, L.-F. et al. Signatures of adaptation in the weedy rice genome. Nat. Genet. 49, 811–814 (2017).
We thank Michael Lin and Tracy Bianco and other members of USDA ARS Dale Bumpers National Rice Research Center and Drs. Miles Lange, and Adam Fuller and their supporting staff members of Harry K. Dupree Stuttgart National Aquaculture Research Center, Amber Delhagen of Pennsylvania State University, Melinda Dalby of Kansas State University, Drs. Lirong Zeng and Bangjun Zhou of University of Nebraska, and Xinglong Chen of China Agricultural University for their excellent technical assistance; and Fanny Liu and Brian Scheffler at USDA ARS Stoneville for all DNA sequencing. For critical reading of this manuscript, we thank Roger Thilmony, Dennis Halterman, Xianming Chen, and Anna McClung of USDA ARS. This project in part is supported by Agriculture and Food Research Initiative Competitive Grant number 2013-68004-20378 (Blast Integrated Project, “BIP”) from the USDA National Institute of Food and Agriculture, USDA-Agricultural Research Service NP301 in-house project, Louisiana Rice Research Board, and The OARDC Research Enhancement Competitive Grants Program (SEEDS) at the Ohio State University. This is contribution number 18-192-J from the Kansas Agricultural Experiment Station. USDA is an equal opportunity employer and provider.
The authors declare no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhao, H., Wang, X., Jia, Y. et al. The rice blast resistance gene Ptr encodes an atypical protein required for broad-spectrum disease resistance. Nat Commun 9, 2039 (2018). https://doi.org/10.1038/s41467-018-04369-4
Plant Disease (2020)
Genome‐wide association study identifies an NLR gene that confers partial resistance to Magnaporthe oryzae in rice
Plant Biotechnology Journal (2020)
Identification of the blast resistance gene Picl(t) from Chaling common wild rice ( Oryza rufipogon Griff.)
Journal of Phytopathology (2020)
Identification and Fine Mapping of Pi69(t), a New Gene Conferring Broad-Spectrum Resistance Against Magnaporthe oryzae From Oryza glaberrima Steud
Frontiers in Plant Science (2020)