Arpita Mishra, Dinesh Pandey, Anshita Goel and Anil Kumar*
Department of Molecular Biology & Genetic Engineering, G. B. Pant University of Agriculture & Technology, Pantnagar
Received Date: July 16, 2010; Accepted Date: August 30, 2010; Published Date: August 30, 2010
Citation: Mishra A, Pandey D, Goel A, Kumar A (2010) Molecular Cloning and In silico Analysis of Functional Homologues of Hypersensitive Response Gene(s) Induced During Pathogenesis of Alternaria Blight in Two Genotypes of Brassica. J Proteomics Bioinform 3: 244-248. doi: 10.4172/jpb.1000146
Copyright: © 2010 Mishra A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Plants possess a vast array of defense strategies to combat pathogen’s growth and colonization. One of the most efficient and immediate defense reactions of plants against the pathogen is the hypersensitive response which is defined as “the rapid death of plant cells in association with restriction of pathogen growth” (Goodman and Novacky, 1994). It is characterized by the presence of brown, dead cells at the site of infection which limits the growth of biotrophic pathogens. HR is a highly concerted complex defense response and is followed by the production of reactive oxygen species (Lamb and Dixon, 1997), modification of ion fluxes (Levine et al., 1996), activation of defense through the synthesis of (Dangl et al., 1996; Dixon et al., 1994) signalling molecules such as jasmonic acid, salicylic acid, protein kinases. Salicylic acid accumulation leads to the onset of systemic acquired resistance in distal plant tissue (Ryals et al., 1996). These events are accompanied by the activation of several plant defense genes, local accumulation of pathogenesis related (PR) proteins, activation of transcription factors, degradation of proteins by the polyubiquitin system and programmed cell death.
Although the molecular mechanism leading to the establishment of HR remains to be obscure, a few components have recently been elucidated. The hsr 203J gene of tobacco which is specially activated during the early stages of incompatible plant/pathogen interaction between tobacco and R. solanacearum has been shown to be a molecular marker of the hypersensitive response (Pontier et al., 1994). The expression of hsr 203J gene has been found to be tightly correlated with HR mediated programmed cell death. For example, the expression of Cladosporium fulvum avirulence avr9 gene product in the tomato line containing the Cf-9 defense resistance gene led to cell death with rapid hsr 203J gene activation (Pontier et al., 1998).
Rapeseed and mustard belonging to family Brassicaceae are one of the most important oilseed crops of India. However, the production and productivity of rapeseed and mustard has been greatly hampered by the disease “Alternaria blight” caused by a semibiotrophic pathogen Alternaria brassicae which is responsible for causing 30-70% yield loss in rapeseed and mustard at different locations of Northern India. Development of disease resistant lines so far, has been unsuccessful due to the absence of known source of resistant germplasm. It is being felt that biotechnological methods can successfully be utilized to develop resistant variety provided that the molecular mechanism of pathogenesis/defense is delineated. The molecular mechanism governing differential defense so far has not been studied at the molecular level implying hypersensitive response in Brassica. Present study is the first attempt to identify the hypersensitive response (hsr 203J) gene homologue triggered during pathogenesis of Alternaria blight in susceptible and tolerant genotypes of Brassica juncea and to perform molecular cloning and in silico analysis for establishing their functional roles.
Seeds of tolerant genotype, Brassica juncea cv. PAB 9511 and susceptible genotype Brassica juncea cv. Varuna were sown in plastic pots under glass house conditions and artificially inoculated by spraying the spore suspension (104 spores ml-1) derived from pure culture of Alternaria brassicae. Inoculated plants were incubated for 3 days in humid chamber at 90-100 percent RH followed by incubation, at the temperature ranging between minimum of 8°C and maximum 22°C. Healthy and infected leaves showing necrosis along with chlorosis symptoms from both varieties were harvested and used as source of plant material which was stored at -80°C until further use.
In order to design primers for amplification of hsr 203J like genes, the nucleotide sequences of different hsr 203J like genes were downloaded from NCBI and subjected to multiple sequence alignment using Mega align module of DNASTAR (Burland, 2000) to obtain a consensus sequences which was used to design primers using Primer3 software programme (Untergasser et al., 2007). The primer sequences used for amplification of hsr homologues from Brassica were 5’GTATTACCATGGCGGAGGATTC3’as forward primer and 5’CGGTGACTATGGGAGGACAAAC3’ as reverse primer having Tm of 62°C and 64°C respectively. The RNA was isolated from infected leaves of susceptible (Varuna) and tolerant genotype (PAB-9511) of Brassica juncea by QIAGEN RNeasy Plant Mini Kit. The RNA obtained was quantified and analyzed on agarose gel electrophoresis (Maniatis et al., 1989). For the isolation of hsr 203J like homologues, RT-PCR reactions were performed using QIAGEN One step RT-PCR kit. The amplified products were analyzed on agarose gel and gel eluted using Genei extraction kit. The amplified products were cloned in pGEMTeasy vector (Promega,USA) as per the kit instructions. Eluted PCR amplicons and cloned fragments were directly sequenced.
The sequenced hsr 203J like genes were subjected to homology search using BLASTX tool of NCBI (http://www.ncbi.nlm.nih.gov) (Pruitt et al., 2007). The gene sequence was translated into six possible reading frames using translate tool. (http://ca.expasy.org/ tools/dna.html). The sequences were further analyzed by software called GENESCAN (Stormo, 2000) and FGENESH (Solovyev et al., 2006) for fishing out the hypothetical protein of that gene. Further, the ORF that might encode this hypothetical protein was revealed by its comparison with the six reading frames. The protein sequence was subjected to protein functional analysis using INTERPROSCAN and PFAM version 23.0 (Finn et al., 2006).The sequences of Brassica hsr 203J like protein along with known hsr 203J like genes from databases were aligned using clustalW (Thompson et al.,1994) and phylogenetic tree was constructed using UPGMA method. A tree was inferred by Bootstrap phylogenetic inference using MEGA3.1 (Tamura et al., 2007). The motifs present in these sequences were analyzed using MEME software version 3.5.7 (Bailey and Gribskov, 1998). For motif analysis, the selection of maximum number of motif was set to 30 with minimum width of 6 amino acids while other factors were of default selection. The predicted gene was compared with BAC clones of Brassica rapa genome for finding out full length gene encoding hsr 203J like protein. Identified four BAC clones were screened for in silico characterization of cis acting elements in upstream region using PLANTCARE tool. For structural comparison, all four hsr 203J like protein sequences were modelled using homology modelling tool, SWISSMODEL. The hsr 203J like protein structures from tolerant and susceptible varieties were visualized and superimposed using SWISSPDB viewer.
In silico analysis of hsr gene homologues
Efforts were made to isolate and clone hsr 203J like homologues from Brassica leaves at late stage of infection of Alternaria blight disease. The expressed hsr 203J like gene sequences from infected leaves of tolerant and susceptible variety of Brassica juncea were amplified by RT-PCR by using gene specific primer. A single amplicon of ~400 bp was observed in Brassica juncea cv Varuna while three amplicons of ~400, 600 and 800 bp were observed in Brassica juncea cv PAB 9511 from infected leaves (Figure 1). All four amplicons obtained were gel eluted, purified and sequenced. All four nucleotide sequences were subjected to BLASTx to reveal the similarity at protein level with other existing hsr 203J like proteins respectively. The predicted hsr 203J like protein sequences from Brassica juncea cv Varuna showed 80% whereas the three sequences designated as hsr 203J R1, hsr 203J R2 and hsr 203J R3 from Brassica juncea cv PAB9511 respectively showed 79%, 70% and 72% homology with Arabidopsis hsr 203J like protein. Hence these sequences were considered to encode the homologues of hsr 203J like proteins in Brassica. These sequences were submitted to NCBI database and were assigned the accession numbers FJ357150, FJ812381, FJ812382 and FJ812383 respectively. The differential induction of hsr 203J gene homologues during HR mediated cell death in response to pathogen infection in susceptible and tolerant cultivars of Brassica juncea suggests its role in defense against Alternaria blight pathogen, however their actual functions are yet to be validated through knock out and knock in based functional approaches.
GENESCAN (Stormo, 2000) and FGENESH (Solovyev et al., 2006) were utilized for fishing out the hypothetical protein of that gene. This hypothetical protein was used as input parameter for INTERPROSCAN and PFAM version 23.0 (Finn et al., 2006) for finding their functional domains. It was observed that the protein sequence possess Alpha/beta hydrolase (abhydrolase) domain (Figure 2) which was also present in all hsr like proteins available in the database.
The αβhydrolase domain was common to a number of hydrolytic enzymes of widely different phylogenetic origin and catalytic function. All the four protein sequences along with known hsr 203J like protein sequences subjected to multiple sequence alignment and phylogenetic tree construction using UPGMA method revealed two major clusters. All four sequences were found to be clustered close to Arabidopsis thaliana hsr 203J like proteins while other lying in other cluster (Figure 3). It is worth to recall here that Arabidopsis thaliana also belongs to Brassicaceae to which Brassica spp. belong. Hence, this analysis reveals the role of species specific hsr 203J like homologues in triggering the defense response against various pathogens.
These sequences were further subjected to MEME program for motif analysis. Motif 2, 3, 12, 14, 7 were found to be conserved in all four hsr 203J like sequence as well as Arabidopsis thaliana bringing them together in one cluster (Figure 4). Motif 2 and 3 encode αβ hydrolase domain and esterase domain which are universally present in all hsr 203J like proteins. Motif 12 which is present in αβ hydrolase domain and in N-myristoylation site of proteins is present only in susceptible variety (Varuna) as well as in Arabidopsis hsr 203J like protein. Myristoylation plays a vital role in membrane targeting and signal transduction in plant responses to environmental stress (Podell and Gribskov, 2004). This motif might be responsible for putting them together in one cluster. Motif 19 is present only in hsr 203J like protein from tolerant genotype (PAB9511) of Brassica juncea and absent in hsr 203J like protein of Varuna as well as of other crop plants (Table 1). Motif 19 encodes protein prenyltransferases alpha subunit, which catalyzes the transfer of an isoprenyl moiety to a cysteine at or near the C-terminus of several eukaryotic proteins. Recent research has led to an explosion of information concerning prenylation signals, prenyl transferase enzymes and the role of prenylation in protein-membrane interactions. Experiments have examined the role of prenylation in protein function and the results suggest that protein prenylation may be involved in facilitating proper sub-cellular localization, promoting protein-protein and protein- membrane interactions and regulating protein function (Cox and Der, 1992). Motif 14 is present in BIG1 domain which is immunoglobulinlike (Ig) domain present in bacterial adhesion molecules involved in pathogenecity. Hence, the presence of motif 14 in hsr 203J like protein is suggestive of their defensive role during pathogenesis. The predicted gene was compared with BAC clones of Brassica rapa genome for finding out full length gene encoding hsr 203J like protein. Four full length hsr 203J like genes were identified in four BAC clones (no KBrB032A21, KBrB034A02, KBrB026C23, KBrB069J04) of Brassica rapa and screened for analysis of cis acting elements in upstream region (-1000/+200) using PLANTCARE tool and trans acting factors in downstream region by plant transcription factor database. Several cis acting elements like W box, TC rich repeats and TATA box which represent sites for interaction of defense and pathogenesis related transcription factors were identified in upstream region of putative hsr 203J like gene present within the BAC clone of Brassica rapa (Figure 5). This finding is supported by observation of similar kinds of cis acting elements in hsr 203J like proteins by other workers. For example, in silico analysis of hsr 203J like sequence in tobacco also revealed the presence of W boxes in promoter region that act as important element required for elicitor responsive expression of defense genes (Rushton and Somssich, 1998). It has been reported that the transcriptional factor called WRKY proteins, bind to W boxes and activate plant defense. In plants, a common TAATNN core motif is known to bind many homeodomain proteins and have been identified in parsley pathogenesis -related gene pr-2 (Korfhage et al., 1995). This motif has been found five times in hsr 203J like promoter in tobacco (Pontier et al., 2001).
|12||Abhydrolase(alpha/ beta hydrolase) N-myristoylation site.||YYHGGGFCLCSVDWQ|
|14||BIG1(bacterial immunoglobulin-like (Ig) domain 1) involved in bacterial pathogenecity||NSDDGWIG|
|19||Protein prenyltransferases alpha subunit||YLYCVAEKDVIKDREMEFC|
Table 1: Multilevel consensus sequences for the MEME defined motifs observed among different hsr203J like proteins.
Analysis of downstream sequence by Plant TFDB tool (Figure 6) indicated the presence of NAC domain which has recently been demonstrated to be present in the proteins involved in mediating various biotic and abiotic stress responses in plants. For example, a few NAC genes, such as At NAC072(RD26), At NAC019 At NAC055 from Arabidopsis (Fujita et al., 2004), Os NAC 6 from rice and Bn NAC from Brassica (Hegedus et al., 2003) were found to be involved in plant’s response to various environmental stresses. Presence of NAC domain in hsr 203J like protein suggests its possible involvement in HR resulting from plant pathogen interaction. This is supported by the recent finding in which Os NAC 4 is found to be induced during HR cell death against Acidovorax avenae in cultured rice cells (Kaneda et al., 2007).
These studies implicated that hsr 203J like proteins of Brassica might be regulated by various intracellular signalling proteins during defense response against Alternaria brassicae pathogen during pathogenesis of Alternaria blight. The modelled protein structures of resistant and susceptible hsr like proteins were visualized and superimposed using SWISSPDB viewer. The results indicate that these proteins differ with each other at several amino acid residues (Figure 7 and Table 2). These structural differences might lead to differential functions of different homologues of hsr 203J like proteins in Brassica during susceptibility and resistance response.
Table 2: Amino acid differences in structures of hsr proteins.
Hypersensitive response, a defense reaction of plants against the pathogen can be studied through analyzing the expression of its marker gene(s) like hsr 203J. Present study reveals the identification and cloning of hsr 203J homologues from tolerant and susceptible genotypes of Brassica juncea through RT-PCR analysis. Interestingly, it is the first report to identify structurally different hsr 203J homologues in response to Alternaria blight infection in Brassica. In silico analysis of the sequences isolated from susceptible and tolerant genotypes of Brassica juncea showed the presence of conserved abhydrolase domain having role in cell death. Motif analysis indicated that motif 19 that functions in prenylation is found exclusively in tolerant genotype and motif 12 having myristoylation site was found in susceptible genotypes. Various defense related important cis and trans acting factors were also found in these homologues. This suggests that these hsr 203J like homologues of Brassica play important role in differential defense response against Alternaria blight- a recalcitrant disease caused by Alternaria brassicae.