An Integrated Approach to Comprehend MYMIV-Susceptibility of Blackgram Cv. T9 Possessing Allele of CYR1, the Cognate R-Gene ()
Received 7 October 2015; accepted 14 February 2016; published 17 February 2016
1. Introduction
Yellow mosaic disease of blackgram (Vigna mungo) is caused by Mungbean yellow mosaic India virus (MYMIV). Successful disease establishment resulted in irregular, chlorotic, yellow patches on the leaves, the characteristic phenotype of MYMIV-infected susceptible plants. The yield penalty reaches to the extent of cent percent when pathogenesis affects MYMIV-susceptible plants at the early stage of development. Interactions between blackgram and MYMIV can lead to establishment of the disease, i.e. compatible response; on the contrary, MYMIV-resistant plants exhibit complete resistance, the phenomenon referred to as incompatibility. In one of our previous studies we have isolated a candidate disease resistance (R) gene, CYR1 that co-segregates with MYMIV-resistant populations of V. mungo [1] . CYR1 that coded in silico translated protein sequence comprised of 1176 amino acids with coiled coil (CC) structure at the N-terminus, central nucleotide binding site (NBS) and C-terminal leucine-rich repeats (LRRs) that belongs to non-TIR (CC)-NBS-LRR subfamily of plant R genes. CYR1 transcripts were unambiguously expressed during incompatible plant virus interactions. Additional molecular and in silico studies suggest involvement of CYR1 in recognizing MYMIV-effector molecule thus contributing incompatible interaction with MYMIV. We have also introgressed this cognate R gene in the MYMIV-susceptible cultivar T9 through molecular breeding and raised number of agronomically useful recombinant inbred lines establishing the biological function of CYR1 [2] . These class of genes encodes CC-NBS- LRR proteins that recognize specific pathogen-derived products and initiate a resistance response that often includes a type of cell death known as the hypersensitive response (HR).
Under this backdrop we questioned the role of allele (cyr1) of CYR1, if any, present in the susceptible Cv. T9. Hence, at first, we detected the presence of an allele of CYR1 in Cv. T9 through Southern hybridization. However, we could neither detect any transcripts of CYR1 by RT-PCR nor by Northern hybridization techniques in the MYMIV challenged Cv. T9 or in segregating susceptible lines (raised by crossing T9 with the MYMIV-re- sistant line). Subsequently, we have isolated the allele through PCR amplification followed by genome walking and sequencing. It was revealed that cyr1 possess truncated N-terminal CC-region. It was suggested by Feys et al. [3] that N-terminus of NBS-LRR proteins influences downstream signaling components after recognizing pathogen effector proteins. The barley (Hordeum vulgare) Mla proteins bind to WRKY transcription factors through their CC domains [4] , although it was not clear that whether such interaction was involved in recognition or signaling. Similarly, N-terminal TIR domain of RPP1A, one of the R proteins of Arabidopsis thaliana plays a crucial role in the cell death signaling pathway [5] . Later, Swiderski et al. [6] have confirmed through a comprehensive study that the TIR domain is indeed an effector domain for cell death signaling, like CC domain.
Nevertheless, the genomic evidences of host-pathogen interaction could not unambiguously explain the inability of expression of cyr1 transcripts even after challenging with the virus, which led us to generate 3D models using comparative modelling of the CYR1 protein from the resistant and cyr1 from susceptible Cv. T9 along with the MYMIV-coat protein (CP), which is the most potent pathogen effector molecule. The models of the CYR1 and cyr1 proteins were then aligned and an alignment Z Score of 0.84 was obtained with an RMSD of 3.6 (Å); which indicated significant structural similarities. These were then docked separately with the MYMIV-CP and analyzed for intermolecular interactions which revealed strong associations involving hydrogen bonded and Van der Waals contact mediated interactions for the CYR1 and MYMIV-CP; and only non-bonded weak Van der Waals interaction between cyr1 and MYMIV-CP.
All these above evidences put together point towards the inability of cyr1 allele of T9 cultivar to confer resistance against MYMIV and hence showed compatible interaction.
2. Materials and Methods
2.1. Plant Materials
The MYMIV-susceptible Vigna mungo, Cv. T9 and MYMIV-resistant line VM1 [7] were grown in the insectary room with suitable growth conditions at the Madhyamgram Experimental Farm (MEF) of Bose Institute, Kolkata, India. In addition, one susceptible inbred line (B20) and two resistant inbred lines (VMR B33 and B38) [2] were used as experimental materials for studying transcript expression of targeted alleles of CYR1 amongst virus challenged V. mungo plants.
2.2. Artificial, Forced Inoculation of V. mungo with MYMIV
Experimental plants were challenged with the viruliferous whiteflies, vector of MYMIV, using the forced feeding method as described by Kundu and Pal [2] . Briefly, white fly populations (B. tabaci) were reared on susceptible blackgram plants, grown in insect proof cages and maintained at 27˚C in the insectary facility of the MEF. About 25 - 30 adult white flies were captured in transparent glass trappers and allowed for an acquisition access period of 24 h on symptomatic leaves of naturally infected blackgram plants. Subsequently, the trappers with viruliferous whiteflies were attached to the leaves of 3-week-old healthy plants of selected experimental lines and allowed to feed for 24 h inoculation access period, thereby transmitting the virus particles from the viruliferous flies to the plant. Likewise another set of experimental plants were forcefully fed by the starved, non-viruliferous whiteflies and referred to as mock inoculated control. Accumulation of MYMIV particles in the host plants after challenging with the virus was determined by qPCR as previously reported by Kundu et al. [8] .
2.3. Isolation of Genomic DNA
DNA was isolated from the seedlings of V. mungo Cv. T9 and MYMIV-resistant line VM1 using modified CTAB method of DNA isolation following Basak et al. [7] . Isolated DNA was quantified in a NanoDropTM 1000 Spectrophotometer (Thermo Scientific, USA) and diluted to a concentration of 0.1 µg/µl. The size and purity was checked by loading 1 µl of sample DNA and 1 µl of control genomic DNA (0.1 µg/µl; supplied with Genome Walking kit, Clontech) on a 0.6% agarose/EtBr gel along with 1 kb Plus DNA ladder (Fermentas, France). The purity of genomic DNA was checked by EcoRV digestion.
2.4. Southern Hybridization
Twenty-five µg genomic DNA was isolated separately from five experimental plants as stated above. These were subjected to restriction digestion with BamHI, EcoRI, HindIII and SmaI, separated on agarose gel and blotted onto a nylon membrane. The objective of these hybridization experiments was to check the presence and copy number of CYR1 and its allele within the whole genomes of VM1 and T9 Cv. respectively.
Following steps were performed sequentially to conduct the hybridization experiments. A PCR fragment amplified from VM1 genomic DNA, using 5’-GGGTGGATTGGGTAAGACCAC-3’ Forward and 5’-TCTGAAAAGTGTGTGGCGCT-3’ Reverse primer combinations. Amplified product was 1235bp length and labeled with αP32dCTP using Prime-a-gene labeling system kit (Promega, USA) as per manufacturer’s instructions. The membrane was incubated at 68˚C in pre-hybridization solution for 3 hr under constant rotation in a hybridization oven (Stuart Scientific, UK). The radio-labeled probe was denatured and added to the membrane and incubated at 68˚C. The membrane was washed on the following day and exposed to X-ray film.
2.5. Isolation of Total RNA
Leaf samples from control and MYMIV-infected plants were collected at 6, 9, 12, 18, 24 and 36 hr after forced inoculation. Experiments were performed three times on different dates to obtain three independent biological replications. Total RNA was isolated from mock inoculated and infected leaf tissues by using the Trizol reagent (Invitrogen, Carlsbad, CA) treated with DNase-I (Sigma-Aldrich, USA) to eliminate traces of genomic DNA and purified using the RNeasy Plant Mini Kit (Qiagen, USA) following manufacturer’s instruction. Integrity of the isolated RNA samples were assessed by agarose gel electrophoresis and purity and quantity of individual samples were determined spectrophotometrically (NanoDropTM 1000 Spectrophotometer, Thermo Scientific, USA).
2.6. Semi-Quantitative RT-PCR Analyses
Expression of CYR1 and its allele, cyr1 were analyzed by RT-PCR method from total RNA of control and MYMIV-infected MYMIV-resistant and -susceptible lines, respectively at 6, 9, 12, 18, 24 and 36 hr. Titan One Tube RT-PCR System (Boehringer Mannheim, USA) was used to synthesize the first strand of cDNA using AMV reverse transcriptase at 50˚C for 30 min followed by the pre-amplification of 10 cycles (denaturation at 94˚C for 30 sec, primer annealing at 60˚C for 30 sec, elongation at 68˚C for 1 min), amplification of 25 cycles with a blend of Taq DNA polymerase and Pwo DNA polymerase (denaturation at 94˚C for 30 sec, primer annealing at 60˚C for 30 sec and primer extension at 68˚C for 1 min with an increment of 5 sec in each cycle) and a final extension at 68˚C for 7 min. At the same time, actin amplification was done with the primers VActin-F (5’-ATGACTCAGATCATGTTTGAG-3’) and VActin-R (5’-AGCCTTCGCAATCCACATCTG-3’) were used in RT-PCR, reaction. The amplified products were analyzed using 1.5% agarose gel electrophoresis and stained with EtBr.
2.7. RNA Blot Hybridization
Total RNA (20 µg) from each sample was separated on a 1.0% agarose-formaldehyde gel and transferred to Hybond-N+Nylone membrane (Amersham, Pharmacia, UK). CYR1 gene specific dCTP-[α-32P]-labelled probe was generated and RNA blot hybridization was performed using the method described above for Southern hybridization.
2.8. Isolation of cyr1 Allele by PCR-Based Genome Walking
T9 cyr1 sequence has been elucidated using genomic DNA from Cv. T9 as template, using Genome Walking kit (Clonetech, USA) following manufacturer’s instruction to obtain full length sequence of the allele. The digested and purified DNA was ligated to Genome Walker Adaptor with T4 DNA ligase at 16˚C overnight in a thermal cycler. The reaction was stopped by adding TE buffer (pH 7.5) and incubated at 70˚C for 5 min, then vortexed at slow speed for 10 sec. The adapter was ligated at both ends of the entire digested product to create Genome Walker libraries. To screen the libraries, primary PCR was set up with outer adapter primer (AP1) and outer gene specific primer (GSP1). Secondary PCR was then set up from primary PCR product with nested adapter primer (AP2) and nested gene specific primer (GSP2). Major PCR product was sequenced in ABI automated DNA sequencer (ABI Prism 3100) and subsequently used for further genome walking using different primers (Table 1), which were designed from conserved regions of CYR1 (Table 1) and different primer combinations were used.
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Table 1. Primers used in genome walking.
2.9. Structural Analysis of Targeted Sequence Using Tools of Bioinformatics
The nucleotide sequence thus obtained was translated using ExPASy translate tool and referred to as cyr1, and conserved domains were analysed using BLASTP and CDS (Conserved Domain Search) tool of NCBI, respectively. To compare cyr1 with CYR1 multiple sequence alignment was done in ClustalW server.
2.10. Secondary Structural Analyses, Comparative Modelling and Simulation
Secondary structural analysis was performed using PSIPRED which uses a simple and accurate secondary structure prediction method, incorporating two feed-forward neural networks which perform an analysis on output obtained from PSI-BLAST (Position Specific Iterated-BLAST). Once the secondary structural features were identified, the proteins were modelled using Modeller 1.12 using multiple comparative modelling. The multiple templates used for the comparative modelling procedure were 4UO8A, 3SFZA, 4TZHA, 4MN8A and 4F3GA for the CYR1 protein and 1Z6TA, 4TZHA, 4FCGA and 4LXRA for the cyr1 protein respectively. Generated structures were subsequently analyzed for their geometries using RAMPAGE server. Following the analyses of geometry the structures were subjected to simulation using the consensus view of protein near-native dynamics obtained from 10-nanosecond MD simulations of all-atom, explicit water, for all protein metafolds using the four most popular force-fields (AMBERff99sb, Consistent Force Field, CHARMM and GROMOS). The model obtained following simulation using AMBERff99sb [9] was found to be the most suitable for further calculations.
2.11. 3D Structure Analyses
Following this the CASTp server was used for the analyses of 3D structural motifs present in the structures. CASTp uses a combination of Delaunay Triangulation scoring scheme based on the basic voronoi diagram architecture which enables the proper detection of concavities and depressions in protein 3D structures along with the calculations of the area and volume of the predicted pockets.
2.12. Fast Fourier Transformation Based Docking
For the study of protein-protein interaction rigid body docking calculations were used in a background Fast Fourier transform (FFT) approach. Here for each molecule encoding of both surface shape and electrostatic charge and potential distributions was modeled using 3D expansions of real orthogonal spherical polar basis functions; which enables the representation of each property by a coefficient vector. The Van der Waals steric density model and the classical electrostatic theory was used for surface calculations and representations. The overlap of parametric functions were represented as expressions to generate the overall docking score as a function of the six degrees of freedom in a rigid body docking search. With suitable scaling factors, this docking score was then interpreted as gradually minimized interaction energy. The docking calculations were performed using HEX and were validated with PATCHDOCK server and filtered through Firedock.
2.13. Studies on Interactions Using DIMPLOT
The DIMPLOT program was used to plot the interactions across the protein-protein interface; i.e. the interface between the CYR1 and MYMIV-CP as well as the interactions between the T9 cultivar cyr1 and MYMIV-CP. The interactions plotted were hydrogen bonds and non-bonded contacts through Van der Waal’s Interactions. They were extracted from the usual HBPLUS output by the program DIMER; and the plot was generated by LIGPLOT.
2.14. In Silico Mutagenesis and Calculation of Interaction Hotspots
In silico mutagenesis was performed using SPDB viewer and the proteins were then simulated using GROMACS. Separate models were generated for each interacting residue. This resulted in 3 different models of the CYR1 protein. However, in case of T9 CYR1 protein no residues were mutated since hydrogen-bonding pattern were not identified. Thus 3 distinct docking calculations were reperformed and hotspots were identified (Amino acid residue―the change which causes ΔΔG > 2.5 kcal/mol change in free energy of docking is accepted to be a hotspot) [10] .
A single residue N112 was found to be present in the unaligned portion of the CYR1 protein which was involved in Van der Waal’s contact with the cognate MYMIV-CP protein. The corresponding segment in the N terminal domain of the cyr1 protein was truncated. To test the importance of this particular residue, it was mutated to alanine, simulated using the Amberff99sb force field and redocked with the MYMIV protein.
3. Results and Discussion
Southern hybridization with labeled “CYR11235” fragment of the digested genomic DNA with all the four different restriction enzymes (BamHI, EcoRI, HindIII and SmaI) revealed presence of single copy CYR1 gene within the genomes of MYMIV-resistant lines of V. mungo, VM1, B30 and B38 (Figures 1(a)-(d)). Faint signals were also observed in the genomes of susceptible cultivar T9 and susceptible line B20. However there were differences in the migration of signals between MYMIV-resistant and -susceptible plants, especially in HindIII digested genomes of susceptible lines, which moved faster in the gel than that of the resistant lines. Thus Southern hybridization revealed presence of an allele of CYR1 in the susceptible Cv. T9 and in the inbred susceptible line B 20, which is referred to as cyr1 allele in the following text.
In order to investigate expression profiles of transcripts of CYR1 after MYMIV infection, reverse transcription PCR was conducted. CYR1 transcripts were expressed in the resistant plants (VM1, B30 and B38) at 9 hpi after virus infection (Figure 2). Highest expression level was observed at 18 and 24 hpi and declined subsequently at 36 hpi. Transcript expression was undetectable in the susceptible plants, Cv. T9 and B20 (Figure 2). None of the mock inoculated and wounded plants showed CYR1 transcript expression (data not shown).
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Figure 1. Southern hybridization analysis of genomic DNA of Vigna mungo, digested with BamHI (a), EcoRI (b), HindIII (c) and SmaI (d), probed with aP32-labeled CYR1 fragment of candidate R genes. Lane number in each blot represents: 1) positive control (PC); 2) T9, MYMIV susceptible cultivar; 3) VM1, MYMIV resistant line; 4) B20, a susceptible inbred line; 5) and 6) B30 and B38 resistant inbred lines. The solid arrows indicate the hybridization signal of the target gene.
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Figure 2. CYR1 transcript accumulation at different hours after MYMIV infection in resistant and susceptible V. mungo plants (upper panel). T9 is the susceptible parent and VM1 is the resistant parent, whereas B20 is a susceptible inbred line and B30 and B38 are the resistant inbred lines of V. mungo. Actin gene amplification by RT-PCR has been shown (lower panel) as positive control from same RNA samples.
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Figure 3. CYR1 transcript expression by Northern hybridization at different hours after MYMIV infection in resistant and susceptible V. mungo plants. Twenty microgram aliquots of total RNA extracted from leaf tip tissues of experimental plants at 0, 3, 6, 9, 12, 18 and 24 hpi were used for northern assay. The blot was hybridized with αP32-labeled CYR1 marker fragment. Equal loading of RNA is shown in ethidium bromide-stained RNA gel (lower panel).
In a previous study we had shown that the candidate resistant gene CYR1 is intron less [1] , hence the allele cyr1 was isolated from the genomic DNA of Cv. T9 by genome walking and submitted to NCBI (GenBank ID: KR350634).
The predicted aminoacid sequence (5’-3’ Translational Frame 1) of cyr1 also shows homology with NBS and LRR domains like that of CYR1 (Figure 4). Although cyr1 has characteristic conserved motifs of CC-NBS- LRR class of disease resistance (R) protein, yet definite mismatches are noted within the sequence when compared with amino acid sequence of CYR1. A stretch of 128 amino acids is absent in N-terminal CC domain (Figure 4). Such truncated N-terminal CC-region indicates functional impairment with respect to the signal transduction presumably even after recognizing the effector protein of the virus. Role of N-terminal CC domain of R protein has been implicated in plant pathogen interaction by several researchers. Moffett et al. [11] have shown activation of R proteins in presence of coat protein of Potato virus X (PVX-CP), which they presumed due to the induction of a conformational change in the CC-type R proteins of potato Rx. They have further demonstrated that the isolated CC domain complemented a copy of Rx lacking NBS-LRR. CC domain complements NBS-LRR leading to pathogen-dependant HR during intramolecular interactions of Rx protein of potato [11] [12] and BS2 protein of Nicotiana benthamiana [13] . Similar inter-domain interactions appear to take place in TIR-NBS-LRR protein as well [14] .
While, in RNBS-A motif, serine of CYR1 is replaced by isoleucine in cyr1; and in RNBS-C phenylalanine residue is replaced by serine (Figure 4). In the C terminal of LRR domain valine, tyrosine and serine is replaced by isoleucine, histidine and phenylalanine, respectively. Also a short stretch of amino acid residues, FVYW, is replaced by LSIG.
3-D structures of CYR1, cyr1 and MYMIV-CP generated using comparative modeling are depicted in Figure 5. Distinct differences in the β-sheet conformations between CYR1 and cyr1 are evident. This is perhaps due to the truncated CC region of cyr1. Although structural alignment between these two plant proteins has conformational similarity (Figure 6).
Molecular recognition is one of the major facets behind the key biological processes that occur in an organism. The molecular switch that operates in plants to recognize pathogen invasion depends on the kind of pathogen [15] . In case of virus pathogens, host’s NBS-LRR genes either induce HR or complete resistance as phenotypic
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Figure 4. Alignment of of CYR1 predictive protein from the MYMIV-resistant genotype of Vigna mungo with cyr1 from MYMIV-susceptible Cv. T9. The underlined region at the start of the alignment indicates the truncated portion of the N-terminal coiled coil domain of the cyr1 sequence, the framed regions indicate the conserved motifs of central NBS domain and LRR repeats at the C-terminal region are shaded. Interacting residues of the cyr1 protein are marked in green and those of the CYR1 protein are marked in blue.
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(c)
Figure 5. 3-D structures of the interacting partners generated using comparative modelling. CYR1 protein (a); cyr1 protein (b) and MYMIV-coat protein (c); Colour schemes according to secondary structural conformations: Yellow: β-sheet, Sea green: ?-helix, forest green: coils.
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Figure 6. Structure alignment between CYR1 protein of MYMIV-resistant and cyr1 of MYMIV-susceptible cultivar showing similar conformations.
response against virus infection [15] . TheHSP90 (heat-shock protein 90) proteins are involved in the protein folding and modulate innate immune responsive proteins in plants [16] - [18] . In a previous study we have shown that in MYMIV-resistant genotype of blackgram HSP 90 was over-expressed at early hours of viral infection than in Cv. T9 [8] . This further indicates the possibility of functional inability of cyr1 in recognizing MYMIV- CP, perhaps due to folding impairment.
Most molecular recognition processes are based on either electrostatic or geometric complementarities. Cellular proteins are involved in their interactions with other cellular proteins or small molecular agonists, antagon- ist cofactors or even drugs. For most of such interactions, there are either one or two or multiple (allosteric) binding sites, which represent a precise 3D conformation that enables the protein to get a good grip of its inte racting molecule. However, the surrounding environment where the interaction is to take place also plays a big role and properties such as pH, ionic strength and ordered water have been reported to influence the binding process [19] .
In this work the efficacy of interactions between the defense protein of blackgram and a viral pathogen, MYMIV-CP was investigated. It was found that the interactions of the two proteins were mediated in the MYMIV-resistant blackgram through two hydrogen bonded and nine Van der Waals contact. The total free energy of interactions was found to be ?1535.1 KJ/mol, indicative of a stable complex (Figure 7). The residues involved in the hydrogen bonded interactions―Lys519 and Thr490 were identified to be present in the largest pocket of the protein. When these residues were replaced with alanine following the principle of in silico mutagenesis, the stability of the formation of the complex suffered as indicated by the lack of formation of the hydrogen bond at the respective positions and the increase in the free energy of complex formation from
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Figure 7. (a): Showing major pockets of CYR1; (b): Showing amino acids involved in the active pockets; (c): Macromolecular complex involving CYR1 and MYMIV coat-protein; (d): Van der Waal’s interactions between CYR1 and MYMIV coat-protein.
−1535.1KJ/Mol to −1237.25 KJ/mol (Lys519Ala) and from −1535.1 KJ/Mol to ?1146.3KJ/mol (Thr490Ala). These results indicate that both the residues were interacting hotspots and played significant role in regulating the interactions of the interacting partners. However, in case of cyr1 and MYMIV-CP interactions, distinct differences were observed: the lack of formation of any intermolecular hydrogen bonds between the two proteins and a marked increase in the total free energy of interactions: 1291.35 KJ/mol. Of the six residues involved in Van der Waals interaction only Lys201 was identified to be present in a predicted pocket of the protein (Figure 8). A domain specific study of interacting residues led to the observation that two residues (marked in green) of the cyr1 protein Asp777 and Thr778 part of the NBS-LRR region are involved in protein-protein interactions whereas only the Ile 558 (marked in blue) of the CYR1 protein NBS-LRR region is involved in Van der Waal’s interaction (Figure 4).
The truncated N terminal coil coiled domain of the cyr1 protein is probably responsible for the lack of conformational stability as an aspartate at position 112 is involved in CYR1-MYMIV interaction which is lacking for the cyr1 protein. This residue when mutated to alanine resulted in alteration of the binding energy from 1535.1 KJ/Mol to −1357.25 KJ/mol, indicating that apart from the hydrogen bonded residues mentioned earlier this residue, is also an important hotspot for the protein-protein interaction and as none of the three hotspot re- sidues are involved in protein binding in case of the cyr1 protein, the efficacy of interaction is poor, resulting in susceptibility.
The present study further augments the observations of Maiti et al. [1] , where we have studied the interactions of the isolated LRR domain of the CYR1 protein and the MYMIV-CP under the backdrop that the LRR domain mediates protein-protein and protein-ligand interactions and is involved in the specific recognition of pathogen-derived elicitors [20] - [22] . Since the work of Maiti et al. [1] was done using only the LRR domain, specific calculations and conformations of the macromolecular complex formation between the cognate interacting partners were not estimated.
Over the years several workers have indicated that true protein-protein interactions when simulated in silico is actually a successful energetic ensemble which has optimized representation and balance of both shape and physico-chemical complementarities, including Van der Waals electrostatic, hydrogen bonding, hydrophobic and solvent interactions [19] [23] . Since in case of cyr1 and MYMIV interactions the complex formation is solely
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Figure 8. (a): Showing major pockets of cyr1; (b): Showing amino acids involved in the active pockets; (c): Macromolecular complex involving cyr1 and MYMIV coat-protein; (d): Van der Waal’s interactions between cyr1 and MYMIV coat-protein.
dependent upon the Van der Waals contacts the stability stands compromised, which is not the case in the interactions between the CYR1 protein and MYMIV-CP. Thus, from the above data we can conclude that the lack of proper molecular recognition of the pathogen effector protein by cyr1 of blackgram Cv. T9 leads to the establishment of host-pathogen compatible interaction. This study also confirms presence of the cyr1 allele of a cognate MYMIV-resistance gene, CYR1 in blackgram Cv. T9.
4. Conclusion
Thus, the present study revealed that due to the truncation in the cognate “R” gene, that recognizes MYMIV effector protein, resulting in structural difference in the N-terminal of CC-domain of the protein cyr1 the widely cultivated T9 variety of blackgram shows compatible interaction with MYMIV, i.e. susceptible to the virus.
Acknowledgements
This work was supported by the Council of Scientific and Industrial Research, New?Delhi, India for the Emeritus Scientist’s Scheme to AP (Sanction No. 21(0884)/12/EMR?II) and also by the Department of Biotechnology, India (Sanction no. BT/01/COE/06/03). We are thankful to the Director, Bose Institute for providing all infrastructural facilities.
NOTES
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*Both these authors are equal contributors.
#Corresponding author.