versão On-line ISSN 1678-4685
Genet. Mol. Biol. v.28 n.3 supl.0 São Paulo 2005
Adriano Barbosa-da-Silva; Ana C. Wanderley-Nogueira; Raphaela R.M. Silva; Luiz C. Berlarmino; Nina M. Soares-Cavalcanti; Ana M. Benko-Iseppon
Universidade Federal de Pernambuco, Centro de Ciências Biológicas, Departamento de Genética, Laboratório de Genética e Biotecnologia Vegetal, Recife, PE, Brazil
A major goal of plant genome research is to recognize genes responsible for important traits. Resistance genes are among the most important gene classes for plant breeding purposes being responsible for the specific immune response including pathogen recognition, and activation of plant defence mechanisms. These genes are quite abundant in higher plants, with 210 clusters found in Eucalyptus FOREST database presenting significant homology to known R-genes. All five gene classes of R-genes with their respective conserved domains are present and expressed in Eucalyptus. Most clusters identified (93) belong to the LRR-NBS-TIR (genes with three domains: Leucine-rich-repeat, Nucleotide-binding-site and Toll interleucine 1-receptor), followed by the serine-threonine-kinase class (49 clusters). Some new combinations of domains and motifs of R-genes may be present in Eucalyptus and could represent novel gene structures. Most alignments occurred with dicots (94.3%), with emphasis on Arabidopsis thaliana (Brassicaceae) sequences. All best alignments with monocots (5.2%) occurred with rice (Oryza sativa) sequences and a single cluster aligned with the gymnosperm Pinus sylvestris (0.5%). The results are discussed and compared with available data from other crops and may bring useful evidences for the understanding of defense mechanisms in Eucalyptus and other crop species.
Key words: serine-threonine kinase, nucleotide binding site, leucine-rich repeats, gene-for-gene interaction.
Pathogen attack can severely affect crop production, with losses that can achieve 80% of the production especially in tropical countries. At the global level, losses have been estimated to accomplish around 12% of the world crop production (James et al., 1990). The most important group of genes that has been used by breeders for disease control is the plant resistance (R) genes: single determinant of an effective and specific resistance that can often be characterized by localized necrosis at attempted infection sites (Rommens and Kishore, 2000).
It is proposed that pathosystems are usually highly specific, with a matching R-gene on vegetal cell that recognizes elicitor proteins (called Avr-effector) of each infective pathogen. Plant will be resistant and the growth of the pathogen will be arrested only when both genes, R and Avr, are present (Ellis et al., 2000a). So, for each R-gene a correspondent Avr gene co-exists: this is the basis of the gene-for-gene concept, suggested by Flor (1956, 1971).
Avirulence gene products actually described do not comprise a defined family of related proteins, since no sharing similar motifs or domains could be found. On the opposite, R-gene products are separated into distinct but related protein classes, according to their conserved structural domains. Conserved domain function identified for R proteins suggests two fundamental mechanisms during pathogenic infection: (I) the pathogen recognition, conducted mainly by leucine-rich repeats (LRR) regions, which play a direct role in protein-protein specific recognition event; and (II) signaling of pathogen presence in order to activate defense related genes (Richter and Ronald, 2000).
The TIR (Toll interleukine 1-receptor) and CC (coiled coil) regions are involved in signal transduction during many cell processes (Martin et al., 2003), while the NBS (Nucleotide Biding Site) usually signalizes for programmed cell death in animal cells (van der Biezen and Jones, 1998). Additionally, a kinase catalytic region is present in some R-genes. This domain plays a direct role in both signaling processes and pathogen effectors. Additionally the NBS region contains not only the three motifs involved in nucleotide binding but additional motifs as well. This extended region of homology is referred to as the NB-ARC domain (Richter and Ronald, 2000). Sometimes this domain contains a distinct predicted nucleoside triphosphatase (NTPase) domain known as NACHT, common in animal, fungal and bacterial proteins, implicated with apoptosis induction and transcription activation (Koonin and Avarind, 2000).
Resistance genes are members of a very large multigene family, are highly polymorphic and have diverse recognition specificities. They are commonly clustered in the genome, often in tandem direct repeats, what is consistent with the theory that they originated through gene duplication and that they are continuously evolving through unequal exchange (Song et al., 1997).
Most of the resistance genes that have been cloned and characterized resemble components involved in signal transduction. These can be classified into five categories based on their predicted protein structure (Song et al., 1997, Ellis and Jones, 1998).
The first class is represented by the Pto gene of tomato, which encodes a protein with a catalytic serine-threonine kinase (ser-thre-kinase) and a myristoylation motif in his amino terminal region (Martin et al., 1993).
The second class comprises many proteins that present a region rich in repetitions of leucine (LRR, Leucine-rich repeats), a Nucleotide Binding Site (NBS) and a leucine zipper (LZ) or a coiled-coil (CC) sequence. Many genes encode proteins of this class: I2 (Ori et al., 1997), Mi (Milligan et al., 1998) and Sw5 (Brommonschenkel et al., 2000) from tomato; RPM1 (Grant et al., 1995), RPP8 (McDowell et al., 1998), RPS2 (Mindrinos et al., 1994) and RPP13 (Bittner-Eddy et al., 2000) from Arabidopsis thaliana; Pib (Wang et al., 1999), Pi-ta (Bryan et al., 2000) and Xa1 (Yoshimura et al., 1998) from Oryza sativa (rice); Gpa2 (Van der Vossen et al., 2000), Hero (Ernst et al., 2002), R1 (Ballvora et al., 2002), Rx1a (Bendahmane et al., 1995) and Rx2 (Bendahmane et al., 2000) from potato; Rp1 from maize (Collins et al., 1999); Mla from barley (Halterman et al., 2001) and Dm3 from lettuce (Meyers et al., 1998).
The third class includes similar proteins as described for class II, presenting a toll receptor for interleukine-I (IL-1R) instead of a CC sequence at the amino terminal region (Meyers et al., 1999). This class is referred as TIR-NBS-LRR, including the genes L (Lawrence et al., 1995), and P (Dodds et al., 2001) of flax; RPP1 (Botela et al., 1998), RPP4 (van der Biezen et al., 2002), RPP5 (Parker et al., 1997) and RPS4 (Gassmann et al., 1999) of A. thaliana and N (Whithan et al., 1996) of tobacco. This class (also present in animals) is supposed to be absent in monocotyledonous plants (Ellis and Jones, 1998), being present in all dicotyledonous taxa actually studied.
The proteins encoded by the three classes of genes previously cited do not present a transmembrane sequence and are therefore classified as intracellular R-proteins (Martin et al., 2003).
The fourth class of resistance genes belongs to the tomato Cf-family, encoding similar proteins with an extracellular LRR and a short cytoplasmatic tail, but no NBS or any further recognizable domain (Dixon et al., 1996). Member of this family are Cf-2 (Dixon et al., 1998), Cf-4 (Joosten et al., 1994; Thomas et al., 1997), Cf-5 (Dixon et al., 1998) and Cf-9 (Jones et al., 1994).
The fifth class includes a single gene, Xa21 from rice that presents an extracellular LRR, a transmembrane region (TM) and a cytoplasmatic ser-thre-kinase. Thus, the structure of Xa21 indicates an evolutionary link between different classes of plant disease resistance genes (Song et al., 1997).
There is still a sixth class that presents genes with no conserved domains, as described for the previous five classes. This group comprises the gene Hm1 from maize, a reductase that confers resistance to the fungus Cochliobolus carbonum (Johal and Briggs, 1992); Mlo from barley, a putative regulator of defense against Blumenaria graminis (Piffanelli et al., 2002) possibly associated to the plasma membrane (Buschges et al., 1997); and RPW8 from A. thaliana, that confers non-specific resistance to the fungus Erysyphe chicoracearum (Xiao et al., 2001).
Due to its qualities as high level of adaptability, fast growing capacity and wood quality, Eucalyptus plantations are carried out in all tropical areas in diverse continents. Eucalyptus is the most widely used tree for delivering raw material for the paper industry used in the production of cellulose and to regenerate degraded areas. Over the past 50 years large-scale planting of fast growing exotic E. grandis, E. urophyla, E. saligna and many hybrids (particularly grandis x urophyla) has occurred in Brazil aiming to reforest some regions and to create an adequate supply of wood, timber and fuel for different purposes (McNabb, 2002). In the late 2001s growing areas reached 138.132 ha, generating more than 7,398 direct employments (BRACELPA, 2004).
The advance of plantations to hot and humid areas resulted in favourable conditions to the development of diseases especially in young individuals that are often severely attacked by fungal (e.g. Mycosphaerella cryptica, Dichomera versiformis, Cylindrocladium spp. and Phaeophleospora epicpccoides) and bacterial pathogens (Barber et al., 2003, Mafia and Alfenas, 2003).
Eucalyptus Genome Sequencing Consortium (FOREST) aimed to identify over 15,000 expressed genes from 100,000 sequenced EST from 19 libraries from specific tissues and stages.
The present work aimed to perform a data mining-based identification of plant disease R-genes in FOREST database, by using well known R-genes sequences as template, comparing the identified sequences with known R-genes deposited in public DNA and protein databases.
Materials and Methods
Amino-acid sequences of known genes have been used as query in the search for R-gene homologues and analogs in Eucalyptus transcriptome database. Accession numbers at NCBI (National Center for Biotechnology Information; http://www.ncbi.nlm.nih.gov) of sequences used are shown in Table 1, together with sequences features and accession numbers. They are grouped according to the conserved domains previously described. Members of the sixth class (reductases and other R-genes with no recognizable conserved domains) have not been included in the present evaluation.
All Eucalyptus sequences used during this work were obtained from FOREST project and derived from cDNA libraries specific to different tissues, organs or conditions of growth from the species E. grandis, E. globulus, E. saligna and E. urophylla. For detailed information see https://forests.esalq.usp.br/Librariesinfo.html.
Reverse alignments were realized on 'FOREST EG_Clusters' database using the program TBLASTN (Altschul et al., 1990), the e-value cutoff adopted was 1e-23. Matching clusters to query sequences were then annotated on a local database called 'non-redundant' made with aid of the Microsoft Access® program. Cluster name was adopted as primary key in order to prevent data redundancy regarding clusters aligning with more than one query sequence. In the few cases when this occurred the name of both queries has been also annotated for the respective cluster.
The clusters frame of the TBLASTN alignment was used to predict the Open Reading Frames (ORFs) for each searched cluster. For this purpose, the Expasy Translate Tool (bo.expasy.org/tools/dna.html) was used, which predicts the correct ORF for a DNA sequence in the corresponding amino acid FASTA sequence. The obtained ORFs were subsequently submitted to a Reverse Position Specific BLAST (RPS-BLAST) against Conserved Domain Database (Marchler-Bauer et al., 2002) aiming to identify patterns or motifs in predicted cluster products.
Reciprocal alignments were conducted for ORFs by downloading the nr databank and stand alone BLAST package from NCBI ftp site for local use at our server (Laboratório de Genética e Biotecnologia Vegetal, UFPE) performing a high-throughput alignment approach. Matched sequences were annotated for latter comparison.
Predictions of subcellular localization have been inferred by using TargetP program available at CBS (Center for Biotechnology Sequence Analysis) Prediction Servers site (http://www.cbs.dtu.dk/services/). Additionally, transmembrane helix segments were inferred with aid of the TMHMM program as well.
After the TBLASTN alignments performed at FOREST EG_Clusters database, a total of 478 clusters aligned with the diverse R-genes (Table 1) used as query (data not showed). These clusters were, as described in section 'Material and Methods', inserted on a local database called 'non-redundant'. This procedure generated a set of 210 non-redundant clusters which have been annotated for one or more than one R-gene (data summarized in Figure 1 and Tables 2 and 3).
Clusters representing exclusive R-gene classes were: (I) serine-threonine kinase (here named KINASE): 49; (II) LRR+NBS: 21; (III) LRR+NBS+TIR: 93; (IV) Only LRR + Transmembrane (LRR+TM): 17 and (V) LRR+TM+ Kinase: 8 (Figure 1).
Regarding the sequence identity of the best alignment, 22 clusters showed equally significant similarity to two different classes of R-genes. From these, 18 included LRR plus LRR-Kinase here called MIX I (sequence data presented in Table 3); three included NBS-LRR plus TIR-NBS-LRR (called MIX II) and one LRR plus Kinase (called MIX III).
Sizes of Eucalyptus clusters aligned to R-genes varied from 3,316 (cluster EGEQRT3301C03 classified to group MIX-III) to 520 nucleotides. The prediction of clusters coding regions revealed that ORFs were coded in both forward and reverse reading frames, with an average of 304 amino acids (aa) in length. ORF sizes varied from 990 (cluster EGEQRT3301C03 of the LRR-KINASE class) to 134aa. Regarding the average ORF length in each R-gene class, we observed 417aa for KINASE, 276aa for NBS, 238aa for TIR-NBS-LRR, 247aa for LRR-TM, 352aa for LRR-KINASE, 372aa for MIX I, 343aa for MIX II and 990aa for MIX III class.
The search for conserved domains (CD-Search) revealed conserved regions (Figure 1, Table 1) in 166 of the 210 here analyzed clusters. A total of 40 clusters presented the kinase domain, 37 of them matched to Pto gene (class I) after the TBLASTN alignment, with only three grouping into KINASE-LRR (two of them) and MIX III (one of them) classes. These two classes also showed associated LRR segments as well. Regarding the LRR domains, these could be identified in 67 different clusters in all classes (except KINASE class I, represented by Pto) with a total of 442 occurrences. This number is higher than the number of clusters due to their occurrence in tandem repetitions. Sometimes these sequences are imperfect and may be difficult to recognize with available in silico tools, so it is possible that a larger number may be identified manually.
Twenty clusters showed the NB-ARC domain. In a specific case, this domain occurred associated to a different TIR domain as was cited above. Additionally, a NACHT domain (closed-related to NB-ARC) was identified exclusively in two TIR-NBS-LRR related clusters (EGCCCL1328B05.g and EGSBRT3118H01).
Most of the 44 clusters with no conserved domains presented shorter ORFs (262 aa in average), with four of them presenting a putative transmembrane region.
A graphic representation of the distribution of conserved domains as compared with class-grouped clusters is presented in Figure 2.
Considering the best matches to the 210 clusters identified, 198 were from plants of Dicotyledonous families, with emphasis on A. thaliana. From monocots only rice (O. sativa) sequences appeared as best matches (11 clusters). One of the sequences from MIX III group aligned with Pinus silvestris (Gymnosperm), the only non-Angiosperm included in the present study. A comprehensive inventory of all species that aligned with Eucalyptus with their taxonomic affiliation and habit (herbaceous or woody) is presented in Table 4.
The post-translational inferences carried out for cluster products (TargetP program) revealed a large number of predictions (Figure 3). The reliability class (RC), which is a confidence measure for the prediction, showed that only 11 sequences were defined into RC1 (higher than 80%), and 53 for RC2 (higher than 60%) class. Most of the sequences are predicted to be located at unspecific subcellular localization (133 sequences) while 35, 20 and 19 were predicted to contain mitochondrial targeting, signal and chloroplast transit peptides, respectively (Figure 3).
After evaluation with the TargetP program, sequences with motifs specific for transmembrane anchoring could be identified in 44 of all analyzed sequences. From these 19 belonged to LRR or LRR-KINASE-related sequences and, unexpectedly, five showed to be TIR-NBS-LRR and 20 to be KINASE-related sequences.
The reverse alignment (TBLASTN) strategy (Altschul et al., 1997) adopted by our group identified a set of 210 clusters similar to the major classes of disease R-genes in the current version of the FOREST database, what comprises 0.63% of the actually generated clusters. This approach allowed the identification of a large set of candidate sequences by using various representative genes per class, while some recent works employed few genes (Koczyk and Chelkowski, 2003). Using several previously described and sequenced R-genes as template was a useful and low-time consuming strategy in the search for R-genes candidates in plants. In this approach it was expected that some similar genes grouped at the same class should cause some level of redundancy (Meyers et al., 1999). The strategy of generating a local database (called non-redundant) by adopting the cluster number as a primary key register was very effective in the solution of this problem. Additionally, this approach was useful in the identification of the respective R-gene class for each Eucalyptus cluster.
The number of R-genes here identified is quite high, especially considering that none of the 19 libraries were obtained under pathogen stress condition. By the other hand, when additional ESTs are generated especially under infection by pathogen, many of the identified clusters may be united in larger clusters of R-genes that may include more domains.
Evidences have shown that R-genes are quite abundant in higher plants, but the most functionally defined R-genes belong to the supergene LRR-NBS family. After completing the whole genome sequencing of the model plant A. thaliana a total of 85 TIR-NBS-LRR have been identified (The Arabidopsis Genome Initiative, 2000), less than the number of clusters (93) actually identified in Eucalyptus. Especially genes containing NBS-LRR domains were estimated to be in number of ca.166 for A. thaliana and ca.600 for rice (O. sativa) by Richly et al. (2002), but this later number is still not confirmed.
A recent work reevaluated and reannotated all NBS-LRR encoding genes in A. thaliana genome database, revealing 149 genes of this class (including 94 TIR and 55 non-TIR sequences) in the genome of A. thaliana (Meyers et al., 2003). In our evaluation of FOREST database we found 114 clusters (93 and 21, respectively) of this class. It is interesting to note that in the evaluation of Meyers et al. (2003) not only the presence of the TIR or of the CC motif was determinant for the grouping of both distinct classes. Also the NBS-LRR domains co-evolved and were determinant in the divergent evolution of the two groups, with the CC-bearing sequences forming four subgroups and the TIR-bearing sequences forming eight subgroups, regarding the size, composition and order or introns and exons.
Pan et al. (2000) compared tomato and Arabidopsis sequences of this class by systematically amplifying the tomato genome using a variety of primer pairs based on ubiquitous NBS motifs, generating 70 sequences, from which 10% were putative pseudogenes. The sequences were also used in mapping approaches, revealing a clustering R-gene homologues between tomato and potato (Solanum tuberosum, also from the Solanaceae family). Clustering of R-genes was also detected in A. thaliana, with most of the genes located in chromosomes 1 (49) and 5 (55), confirming the initial hypothesis that these genes are clustered in few chromosomes (The Arabidopsis Genome Initiative, 2000). This fact was also observed in other crops, as chickpea (Cicer arietinum; Benko-Iseppon et al., 2003). In this last case, with some synteny and colinearity within this species and Arabidopsis. The clustering of R-genes in specific chromosomes and the existence of conserved domains have allowed the establishment of interesting strategies for identification, mapping and breeding directed to the incorporation of such genes from wild relatives. Considering the number of genes from this group in this last species, it is to expect that they are also clustered in Eucalyptus, what can also be valuable for the establishment of Eucalyptus breeding strategies in the future, especially considering the previous existence of mapping populations for this crop.
Overall annotation revealed that Arabidopsis also carries homologues of other R-gene classes, including 174 genes encoding LRR-kinases (Xa21 group), but many of which are likely to play a role in development rather than defense (Jones, 2001). The present work revealed only eight clusters with significant homology to Xa21 but this number can increase if only the kinase sequence is used as template, since the LRR may be quite variable between rice and Eucalyptus. Exceptional R-genes have proven to provide durable disease control, due to the fast evolving pathogen genome that breaks resistance. The Xa21 gene is an important exception to this rule that reveals the full potential of R-genes for breeding purposes (Rommens and Kishore, 2000). This may be very valuable especially considering the possibility of pyramidization of such genes in important crops, increasing the potentiality of an effective specific R-Avr intection.
Another abundant family of R-genes in plants is the ser-thr-kinase with about 50 genes in Arabidopsis encoding protein kinases that are strongly homologous to tomato's Pto gene (Jones, 2001). In Eucalyptus we found almost the same number (49) of clusters also with high homology to the Pto sequence.
Regarding R-gene classes identified in Eucalyptus, an interesting phenomenon was observed in the present work: R-genes pertaining to different classes were able to align significantly to the same cluster on Eucalyptus database. This can be explained by the evidences that known R-genes combine a limited number of related functional domains (Ellis et al., 1999, 2000a). Then, similar motifs would be present in different R-genes, and it is possible that a gene resembling to a determined class may search another belonging to a different class by local similarity at the site of the conserved motif. But in the practice, previous works do not speculate this possibility, once that the genes identified for specific R-genes are directly assigned to its own class as shown by evidences raised from works previously reported (Ronald, 1997; Jones, 2001; Romeis, 2001).
The MIX class one (MIX I) included 18 clusters resembling to genes which belong to both LRR and LRR-KINASE classes. These clusters were searched basically by using Cf (Jones et al., 1998) and Xa21 (Song et al., 1995) amino acid sequences as queries. In this case, the most plausible explanations would be the presence of the LRR domain, common to both classes, being responsible for the alignment and grouping of some clusters in both classes. By the other hand, LRRs are referred as fast evolving sequences and are in some cases quite imperfect, making manual annotation necessary. Often their amino-acid sequences are quite specific to their gene group (Dixon et al., 1998; Ellis et al., 1999). For example, using the LRR of Xa21 against GenBank database will reveal significant alignments only to Xa21 genes of rice (and some other Poaceae) and less significantly to Arabidopsis, but no sequence including other gene classes align significantly. A similar approach to the present work was used for the analysis of SUCEST (Sugarcane EST project, also running in Brazil) database (Morais, 2003) with no similar results. Song et al., (1997) suggested that the structure of Xa21 (here referred as class V) itself indicates an evolutionary link between different classes (I and IV) of plant disease resistance genes. May this be the case of this cluster that present a new link between two classes and can represent a new gene for Angiosperms?
Another surprising result was obtained by analyzing the unique cluster with both domains LRR and KINASE. It would be expected to find both domains in genes resembling Xa21 but this cluster (EGEQRT3301C03.g) showed itself similar to both Pto (class I, described by Martin et al., 1993) and Cf (Class IV, described by Jones et al, 1994) genes. This double similarity occurred on different motifs. The Pto gene is known to encode a ser-thre-kinase protein (Martin et al., 1993) and it was at this motif that the cluster showed similarity to this gene. On the other hand, Cf genes encode extracellular LRRs and it was at the LRR motif that the similarity was found. This cluster could be grouped in the LRR-KINASE class. So, why did it not align with Xa21, the single known gene with both LRR-KINASE domains? It should be answered by analyzing the KINASE-related clusters. Despite of the conservation of this region (Romeis, 2001), none of the Pto (KINASE) or Xa21 (LRR and a receptor-KINASE) related clusters were mixed (aligned together) during the annotation process. This shows that the kinase segment is less-redundant than LRR at least during our in silico gene prediction, once that the kinase CD is present in both Pto and Xa21 genes, they do not caused the mixture of their matching clusters on a mixed class.
The last case of mixture occurred to MIX class II including the motif TIR-NBS-LRR. Two of the three clusters pertaining to this mixed class (EGEQST6001H02.g and EGJECL1208G03.g) were searched at the FOREST database by the genes RPP5 (TIR-NBS-LRR; Parker et al., 1997) and RPS5 (NSB-LRR; Noel et al., 1999). The third cluster (EGEZRT3006B12.g) was obtained through search using RPP5 and RPS4 (both TIR-NBS-LRR; Gassmann et al., 1999) and I2 (NBS-LRR; Simmons et al., 1998) queries. We initially supposed that the redundancy was due to the presence of NB-ARC (NBS) conserved motif. However, the first two clusters did not show any motif after in silico CD-search and, again, the region that apparently caused the mixture of the classes was the LRR motif, once that it was predicted in cluster EGEZRT3006B12.g.
In view of the results discussed above, could we speculate that Eucalyptus bears some new classes of R-genes? Before taking further conclusions and in order to solve the questions raised by the present work, we intend to evaluate these groups of clusters in regard to their domain and interdomain structure and organization, evaluating also the clusterization process, before taking further conclusions.
The conserved domains (CDs) identified during our investigation showed that most of the Eucalyptus predicted sequences possess the same motifs shared by disease R-genes. The CD with the higher level of sampling was LRR, which was present in all classes (except KINASE class I, represented by Pto) with a total of 442 occurrences. The other frequent domain shared by R-genes, the NB-ARC, was observed in 27 sequences, notably in TIR-NBS-LRR and NBS-LRR predicted clusters. This motif is commonly found in such sequences, and it is proposed that NB-ARC plays a role in activation of downstream effectors (van der Biezen and Jones, 1998) by their sequence similarity to mammalian CED-4 and APAF-1 proteins which are involved in apoptosis (Chinnaiyan et al., 1997). In plants the TIR motif is found only associated to NBS regions of dicotyledones, being possibly absent in monocotyledones (Meyers et al., 1999). In Eucalyptus (a eudicot genus of the Myrtaceae family) TIR domains were quite abundant, as expected, being found in 39 clusters (all from TIR-NBS-LRR-class).
Another very common motif present in two classes of disease R-genes is the kinase domain. This motif is shared by Pto (ser-thre-kinase) and Xa21 (receptor-kinase) genes, members of the KINASE and LRR-KINASE classes, respectively. We found that all kinase domains found were associated to the classes KINASE, LRR-KINASE and MIX III. As commented here, despite of its conservation, this domain generally does not cause redundancy while searching in databases.
Transmembrane motifs were found only in 44 of all analyzed sequences. Of these clusters five TM were, unexpectedly, found in TIR-NBS-LRR-related sequences (a group of R-genes that acts at the intracellular level), while the remaining 19 were as expected LRR or LRR-KINASE-related sequences.
Information regarding the localization of disease resistance proteins in plant cells is still scarce (Martin, 1999). Spatial organization is usually variable among distinct gene classes and tissues affected, and there are no strong evidences in favor of conserved correspondence between R and Avr products spatial occurrence (Bonas and Lahaye, 2002). However, immunocytochemistry approaches allowed the subcellular localization of some Avr and R components (Boyes et al., 1998). Here, we adopted an in silico approach which uses neural network-based methods to predict the topology (i.e. localization) of protein sequences of the selected clusters. In spite of the large number of predictions obtained, only 11 sequences were defined into RC1 (reliability class 1 > 80%), and 53 for RC2 (> 60%). Of these significant predictions, we observed that neural network was able to predict the localization of only a small number of proteins (29.62%) compared to the total sample of Eucalyptus R-genes. This percentage of representation is much lower than the 80% obtained for plant test sets carried out by Emanuelsson et al. (2000) with the same approach. It is important to note that these predictions are based on the N-terminal information available for sequences. Thus, this low number of predictions can be explained by the fact that the FOREST database was obtained from expressed sequence tags, an approach that usually do not include N-termini for many EST generated.
Our Eucalyptus transcriptome cDNA sequence analysis revealed that there are 210 clusters with significant alignment to major classes of plant disease R-genes. Differentially from the other genomic efforts, as O. sativa (Goff et al., 2002) we used a redundant set of well described R-genes to screen for RGAs (Resistance Genes Analogs) on FOREST database. This proved to be a very sensitive approach, since best matches in NCBI present sometimes annotation mistakes and we also observed during the present work that some of the best GenBank matches to Eucalyptus R-clusters presented no conclusive description of function. This was also the case also of the first annotation of Arabidopsis genome sequences, as pointed out by Meyers et al., (2003). After reannotation of NBS-LRR sequences a total of 56 of the A. thaliana R-genes had to be corrected from earlier evaluations on GenBank (Meyers et al., 2003). These results show how important procedures as annotation and detailed evaluation of generated sequences are. These evidences bring to reflections about the strategic design of many genome and transcriptome projects, considering that the data mining is not expensive (normally only fellowships are needed) but still receive few investments from financing agencies, diminishing the final impact of the results.
The comparison of our results regarding the number (and maybe the organization) of identified Eucalyptus clusters was mainly with A. thaliana, especially due to the lack of open databases for other plant species with EST projects. Many differences considering the here analyzed R-related sequences can be explained by using diverse arguments: (i) The larger genome of Eucalyptus (e.g. E. grandis with 640 Mbp; Myburg et al., 2003) in contrast with the small and "compact" genome of A. thaliana (120 Mbp) (ii) The distant taxonomic position: both are dicots, but distantly related families (Brassicaceae and Myrtaceae) and finally (iii) the different levels of complexity: Eucalyptus is a wood perennial plant species and Arabidopsis is an annual herb. Herbaceous species are often regarded as faster evolving than woody species considering different morphological and genetic aspects (Bennet, 1972, Enrendorfer, 1982, Morawetz 1984, 1986, Bennet and Leitch, 1995, 2000).
Considering these evidences we observed that most of the information regarding R-genes available in databases refer to herbaceous (not woody) crop plants (few wild plants), maybe because most identified and sequenced R-genes were consequence of mapping approaches that are very time consuming in woody plants and difficult to realize in open pollinated species. The larger number of sequences from A. thaliana representing best alignments to Eucalyptus does not represent a higher similarity to this plant species, moreover it reflects the large number of sequences of this model plant deposited in GenBank. In our evaluation, only 23 woody species appeared as best matches for the clusters studied, including 22 species from different dicotyledonous families and one Gymnosperm species (Pinus sylvestris). This may justify some of the surprising results obtained in the present work and suggest that identification of R-genes in a larger number of taxonomic groups may be a very promissory approach to understand the natural evolution of these sequences when not affected by the influence of man. Regarding the actual knowledge of R-gene structure and diversity, some authors suggested that this gene class evolves faster than other genes (Ellis et al., 2000b) what should be evaluated in a larger number of taxonomic entities including wild species and also primitive taxa.
Using bioinformatic tools it was possible to identify classify and verify the actually sequenced R-genes in Eucalyptus transcriptome. No previous sequences of this type could be found in protein or nucleotide databases for this crop. The identified sequences will be valuable resources for the development of markers for molecular breeding and identification of RGAs (resistance gene analogs) in Eucalyptus and other related species. The identified clusters constitute also excellent probes for physical mapping of genes in this species, giving support to genetic mapping programs and synteny studies. Considering the size of some clusters, they may also be used for fluorescent in situ hybridization (FISH) on Eucalyptus chromosomes, helping also in the comparison of different parental species and the respective hybrids.
The present work on Eucalyptus, based on FOREST database brought some light to the existing R-gene group in this important crop species and also regarding resistance response in higher plants, leading to the following conclusions:
All five gene classes of R-genes with their respective conserved domains are present and expressed in Eucalyptus.
Some new combinations of domains and motifs of R-genes may be present in Eucalyptus and could represent novel R-gene structures, what should be analyzed in detail.
Despite the lack of libraries from tissues ellicitated by pathogens a high number of R-genes was found in different libraries of FOREST project. This may suggest, that the identified clusters are expressed constitutively but also leads to the supposition that a higher number of R-genes may be present in Eucalyptus under other experimental conditions.
Besides the detailed analysis of different groups of genes and domains we intend to evaluate the expression of the selected clusters in the different libraries of the project. Furthermore, some additional efforts may be necessary to complete some sequences of R-genes, especially considering that their size vary between 321 (in case of Pto) and 1802 amino-acids (in case of Xa1 gene) and many identified sequences possibly present incomplete domains.
Further in silico, in vitro and in vivo evaluations of Eucalyptus genome may be a very promissory approach. Manipulation of the expression of these genes in economically important woody plant species aiming to improve disease resistance is necessary. Despite of the challenge that this mission may represent, some reports indicate that this strategy is feasible.
The present authors thank Ms. David Anderson de Lima Morais and Dr. Valdir Queiroz Balbino for interesting discussions and instructions about some of the programs and tools used in the present work. To Dr. Reginaldo de Carvalho and Claudete Maria Marques da Silva we thank for valuable technical support. We thank also CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) for the concession of a fellowship to the last author (Grant no. 478895/2003).
Altschul SF, Gish W, Miller W, Myers EW and Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403-410. [ Links ]
Altschul SF, Madden TL, Schaffer AA, Zhang J, Mille W and Lipman DJ (1997) Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res 25:3389-3402. [ Links ]
Ballvora A, Ercolano MR, Weiss J, Meksem K, Bormann CA, Oberhagemann P, Salamini F and Gebhardt C (2002) The R1 gene for potato resistance to late blight (Phytophthora infestans) belongs to the leucine zipper/NBS/LRR class of plant resistance genes. Plant J 30:361-371. [ Links ]
Barber PA, Smith IW and Keane PJ (2003) Foliar diseases of Eucalyptus spp. grown for ornamental cut foliage. Austral Plant Pathol 32:109-111. [ Links ]
Bendahmane A, Kohn BA, Dedi C and Baulcombe DC (1995) The coat protein of potato virus X is a strain-specific elicitor of Rx1-mediated virus resistance in potato. Plant J 8:933-941. [ Links ]
Bendahmane A, Querci M, Kanyuka K and Baulcombe DC (2000) Agrobacterium transient expression system as a tool for the isolation of disease resistance genes: Application to the Rx2 locus in potato. Plant J 21:73-81. [ Links ]
Benko-Iseppon AM, Winter P, Huettel B, Staginnus C, Muehlbauer FJ and Kahl G (2003) Molecular markers closely linked to fusarium resistance genes in chickpea show significant alignments to pathogenesis-related genes located on Arabidopsis chromosomes 1 and 5. Theor Appl Genet 107:379-386. [ Links ]
Bennett MD (1972) Nuclear DNA content and minimum generation time in herbaceous plants. Proc R Soc Lond Bot 181:109-135. [ Links ]
Bennet MD and Leitch IJ (1995) Nuclear DNA Amounts in Angiosperms. Ann Bot 76:113-176. [ Links ]
Bennet MD and Leitch, IJ (2000) Variation in nuclear DNA amount (C-value) in monocots and its significance. In: Wilson KL and Morrison DA (eds) Monocots: Systematics and Evolution. 1st edition. CSIRO Publishers, Sydney, pp 137-146. [ Links ]
Bittner-Eddy PD, Crute IR, Holub EB and Beynon JL (2000) RPP13 is a simple locus in Arabidopsis thaliana for alleles that specify downy mildew resistance to different avirulence determinants in Peronospora parasitica. Plant J 21:177-88. [ Links ]
Bonas U and Lahaye T (2002) Plant disease resistance triggered by pathogen-derived molecules: Refined models of specific recognition. Curr Opin Microbiol 5:44-50. [ Links ]
Botella MA, Parker JE, Frost LN, Bittner-Eddy PD, Beynon JL, Daniels MJ, Holub EB and Jones JD (1998) Three genes of the Arabidopsis RPP1 complex resistance locus recognize distinct Peronospora parasitica avirulence determinants. Plant Cell 10:1847-1860. [ Links ]
Boyes DC, Nam J and Dangl JL (1998) The Arabidopsis thaliana RPM1 disease resistance gene product is a peripheral plasma membrane protein that is degraded coincident with the hypersensitive response. Proc Natl Acad Sci USA 95:15849-15854. [ Links ]
BRACELPA (2004), Associação Brasileira de Celulose e Papel. Brazil. Available from World Wide Web: http://www. bracelpa.org.br, release date 20/March/2004, cited 25/April/ 2004.
Brommonschenkel SH, Frary A and Tanksley SD (2000) The broad-spectrum tospovirus resistance gene Sw-5 of tomato is a homolog of the root-knot nematode resistance gene Mi. Mol Plant-Microbe Interact 13:1130-38. [ Links ]
Bryan GT, Wu KS, Farrall L, Jia Y, Hershey HP, McAdams SA, Faulk KN, Donaldson GK, Tarchini R and Valent B (2000) A single amino acid difference distinguishes resistant and susceptible alleles of the rice blast resistance gene Pi-ta. Plant Cell 12:2033-2046. [ Links ]
Buschges R, Hollricher K, Panstruga R, Simons G, Wolter M, Frijters A, van Daelen R, van der Lee T, Diergaarde P, Groenendijk J, Topsch S, Vos P, Salamini F and Schulze-Lefert P (1997) The barley Mlo gene: A novel control element of plant pathogen resistance. Cell 88:695-705. [ Links ]
Chinnaiyan AM, Chaudhary D, O'Rourke K, Koonin E and Dixit M (1997) Role of CED-4 in the activation of CED-3. Nature 388:728-729. [ Links ]
Collins N, Drake J, Ayliffe M, Sun Q, Ellis J, Hulbert S and Pryor T (1999) Molecular characterization of the maize Rp1-D rust resistance haplotype and its mutants. Plant Cell 11:1365-1376. [ Links ]
Dixon MS, Jones JGD, Keddie JS, Thomas CM, Harisson K and Jones JGD (1996) The tomato Cf-2 disease resistance locus comprises two functional genes encoding leucine-rich repeat proteins. Cell 84:451-459. [ Links ]
Dixon MS, Hatzixanthis K, Jones DA, Harisson K and Jones JGD (1998) The tomato Cf-5 disease resistance gene and six homologs show pronounced allelic variation in leucine-rich repeat copy number. Plant Cell 10:1915-1925. [ Links ]
Dodds P, Lawrence G and Ellis J (2001) Six amino acid changes confined to the leucine-rich repeat beta-strand/beta-turn motif determine the difference between the P and P2 rust resistance specificities in flax. Plant Cell 13:163-78. [ Links ]
Ehrendorfer F (1982) Speciation patterns in woody angiosperms of tropical origin. In: Barigozzi C (ed) Mechanisms of Speciation. Alan R. Liss. Inc., New York, pp 479-509. [ Links ]
Ellis J and Jones D (1998) Structure and function of proteins controlling strain-specific pathogen resistance in plants. Curr Opin Plant Biol 1:288-293. [ Links ]
Ellis JG, Lawrence GJ, Luck JE and Dodds N (1999) Identification of regions in alleles of the flax rust resistance gene L that determines differences in gene-for-gene specificity. Plant Cell 11:495-506. [ Links ]
Ellis J, Dodds P and Pryor T (2000a) The generation of plant disease resistance genes specificities. Trends Plant Sci 5:373-379. [ Links ]
Ellis J, Dodds P and Pryor T (2000b) Structure, function and evolution of plant disease resistance genes. Curr Opin Plant Biol 3:278-284. [ Links ]
Emanuelsson O, Nielsen H, Brunak B and von Heijne G (2000) Predicting subcellular localization of proteins based on their N-terminal amino acid sequence. J Mol Biol 300:1005-1016. [ Links ]
Ernst K, Kumar A, Kriseleit D, Kloos DU, Phillips MS and Ganal MW (2002) The broad-spectrum potato cyst nematode resistance gene (Hero) from tomato is the only member of a large gene family of NBS-LRR genes with an unusual amino acid repeat in the LRR region. Plant J 31:127-136. [ Links ]
Flor HH (1956) The complementary genetic systems in flax and flax rust. Adv Genet 8:29-54. [ Links ]
Flor HH (1971) Current status of the gene-for-gene concept. Annu Rev Plant Pathol 9:275-296. [ Links ]
Gassmann W, Hinsch ME and Staskawicz BJ (1999) The Arabidopsis RPS4 bacterial-resistance gene is a member of the TIR-NBS-LRR family of disease-resistance genes. Plant J 20:265-277. [ Links ]
Goff SA, Ricke D, Lan TH, Presting G, Wang R, Dunn M, Glazebrook J, Sessions A, Oeller P, Varma H, Hadley D, Hutchison D, Martin C, Katagiri F, Lange BM, Moughamer T, Xia Y, Budworth P, Zhong J, Miguel T, Paszkowski U, Zhang S, Colbert M, Sun WL, Chen L, Cooper B, Park S, Wood TC, Mao L, Quail P, Wing R, Dean R, Yu Y, Zharkikh A, Shen R, Sahasrabudhe S, Thomas A, Cannings R, Gutin A, Pruss D, Reid J, Tavtigian S, Mitchell J, Eldredge G, Scholl T, Miller RM, Bhatnagar S, Adey N, Rubano T, Tusneem N, Robinson R, Feldhaus J, Macalma T, Oliphant A and Briggs S (2002) A draft sequence of the rice genome (Oryza sativa L. ssp. japonica). Science 296:92-100. [ Links ]
Grant MR, Godiard L, Straube E, Ashfield T, Lewald J, Sattler A, Innes RW and Dangl JL (1995) Structure of the Arabidopsis RPM1 gene enabling dual specificity disease resistance. Science 269:843-846. [ Links ]
Halterman D, Zhou F, Wei F, Wise RP and Schulze-Lefert P (2001) The MLA6 coiled-coil, NBS-LRR protein confers AvrMla6-dependent resistance specificity to Blumeria graminis f. sp. hordei in barley and wheat. Plant J 3:335-348. [ Links ]
James WC, Teng PS and Nutter FW (1990) Estimated losses of crops from plant pathogens. In: Pimentel D (ed) CRC Handbook of Pest Management, CRC Press, Boca-Raton, pp 15-50. [ Links ]
Johal GS and Briggs SP (1992) Reductase activity encoded by the HM1 disease resistance gene in maize. Science 158:958-987. [ Links ]
Jones DA, Thomas CM, Hammond-Kosac KE, Balint-Kurti J and Jones JGD (1994) Isolation of the tomato Cf-9 gene for resistance to Cladosporium fulvum by transposon tagging. Science 266:789-793. [ Links ]
Jones DG (2001) Putting the knowledge of plant disease resistance genes to work. Curr Opin Plant Biol 4:281-287. [ Links ]
Jones JB, Stall RE and Bouzar H (1998) Diversity among xanthomonads pathogenic on pepper and tomato. Ann Rev Phytopathol 36:41-58. [ Links ]
Joosten MH, Cozijnsen TJ and De Wit PJ (1994) Host resistance to a fungal tomato pathogen lost by a single base-pair change in an avirulence gene. Nature 367:384-386. [ Links ]
Koczyk G and Chelkowski J (2003) An assessment of the resistance gene analogues of Oryza sativa ssp. japonica, their presence and structure. Cell Mol Biol Lett 8:963-972. [ Links ]
Koonin EV and Aravind L (2000) The NACHT family - A new group of predicted NTPases implicated in apoptosis and MHC transcription activation. Trends Biochem Sci 25:223-224. [ Links ]
Lawrence GJ, Finnegan EJ, Ayliffe MA and Ellis JG (1995) The L6 gene for flax rust resistance is related to Arabidopsis bacterial resistance gene RPP2 and tobacco viral gene N. Plant Cell 7:1195-1206. [ Links ]
Mafia RG and Alfenas AC (2003) Diferenciação sintomatológica de manchas foliares em Eucalyptus spp. causadas por patógenos fúngicos e bacterianos. Fitopatol Bras 28:688-688. [ Links ]
Marchler-Bauer A, Panchenko AR, Shoemaker BA, Thiessen PA, Geer LY and Bryant SH (2002) CDD: A database of conserved domain alignments with links to domain three-dimensional structure. Nucl Acids Res 30:281-283. [ Links ]
Martin GB (1999) Functional analysis of plant disease resistance genes and their downstream effectors. Curr Opin Plant Biol 2:273-279. [ Links ]
Martin GB, de Vicente MC and Tanksley SD (1993) Hight resolution linkage analysis and physical characterization of the Pto bacterial locus in tomato. Mol Plant-Microbe Interact 6:26-34. [ Links ]
Martin GB, Bogdanove AJ and Sessa G (2003) Understanding the functions of plant disease resistance proteins. Annu Rev Plant Physiol Plant Mol Biol 54:23-61. [ Links ]
McDowell JM, Dhandaydham M, Long TA, Aarts MG, Goff S, Holub EB and Dangl JL (1998) Intragenic recombination and diversifying selection contribute to the evolution of downy mildew resistance at the RPP8 locus of Arabidopsis. Plant Cell 10:1861-1874. [ Links ]
McNabb K (2002) Clonal propagation of Eucalyptus in Brazilian nurseries. In: Dumroese RK, Riley LE and Landis TD (eds) National Proceedings: Forest and Conservation Nursery Associations. USDA Forest Service, Rocky Mountain Research Station, Ogden, pp 165-168. [ Links ]
Meyers BC, Chin DB, Shen KA, Sivaramakrishnan S, Lavelle DO, Zhang Z and Michelmore RW (1998) The major resistance gene cluster in lettuce is highly duplicated and spans several megabases. Plant Cell 10:1817-32. [ Links ]
Meyers BC, Diekcman AW, Michelmore RW, Sivaramakrishnan S, Sobral BW and Young ND (1999) Plant disease resistance genes encodes members of an ancient and diverse protein family within the nucleotide-biding superfamily. Plant J 20:317-332. [ Links ]
Meyers BC, Kozik A, Griego A, Kuang H and Michelmore RW (2003) Genome-wide analysis of NBS-LRR-encoding genes in Arabidopsis. Plant Cell 15:809-834. [ Links ]
Milligan SB, Bodeau J, Yaghoobi J, Kaloshian I, Zabel P and Williamson VM (1998) The root knot nematode resistance gene Mi from tomato is a member of the leucine zipper, nucleotide binding, leucine-rich repeat family of plant genes. Plant Cell 10:1307-19. [ Links ]
Mindrinos M, Katagiri F, Yu GL and Ausubel FM (1994) The A. thaliana disease resistance gene RPS2 encodes a protein containing a nucleotide-biding site and leucine-rich repeats. Cell 78:1089-1099. [ Links ]
Morais DAL (2003) Análise bioinformática de genes de resistência a patógenos no genoma da cana-de-açúcar. Master Dissertation, Universidade Federal de Pernambuco, Recife. [ Links ]
Morawetz W (1984) How stable are genomes of tropical woody plants? Heterozygosity in C-banded Karyotypes of Porcelia as compared with Annona (Annonaceae) and Drymys (Winteraceae). Pl Syst Evol 145:29-39. [ Links ]
Morawetz W (1986) Remarks on karyological differentiation patterns in tropical woody plants. Pl Syst Evol 152:49-100. [ Links ]
Myburg AA, Griffin AR, Sederoff RR and Whetten RW (2003) Comparative genetic linkage maps of Eucalyptus grandis, Eucalyptus globulus and their F1 hybrid based on a double pseudo-backcross mapping approach. Theor Appl Genet 107:1028-1042. [ Links ]
Noel L, Moores TL, van Der Biezen EA, Parniske M, Daniels MJ, Parker JE and Jones JD (1999) Pronounced intraspecific haplotype divergence at the RPP5 complex disease resistance locus of Arabidopsis. Plant Cell 11:2099-2112. [ Links ]
Ori N, Eshed Y, Paran I, Presting G, Aviv D, Tanksley S, Zamir D and Fluhr R (1997) The I2C family from the wilt disease resistance locus I2 belongs to the nucleotide binding, leucine-rich repeat superfamily of plant resistance genes. Plant Cell 9:521-532. [ Links ]
Pan Q, Liu YS, Budai-Hadrian O, Sela M, Carmel-Goren L, Zamir D and Fluhr R (2000) Comparative genetics of nucleotide binding site leucine-rich repeat resistance gene homologues in the genomes of two dycotyledons: Tomato and Arabidopsis. Genetics 155:309-322. [ Links ]
Parker JE, Coleman MJ, Dean C and Jones JGD (1997) The Arabidopsis downy mildew resistance gene RPP5 shares similarity to the Toll and interleukin-1 receptors with N and L6. Plant Cell 9:879-894. [ Links ]
Piffanelli P, Zhou F, Casais C, Orme J, Jarosch B, Schaffrath U, Collins NC, Panstruga R and Schulze-Lefert P (2002) The barley MLO modulator of defense and cell death is responsive to biotic and abiotic stress stimuli. Plant Physiol 129:1076-1085. [ Links ]
Richly E, Kurth J and Leister D (2002) Mode of amplification and reorganization of resistance genes during recent Arabidopsis thaliana evolution. Mol Biol Evol 19:76-84. [ Links ]
Richter TE and Ronald PC (2000) The evolution of disease resistance genes. Plant Mol Biol 42:195-204. [ Links ]
Romeis T (2001) Protein kinases in the plant defense response. Curr Opin Plant Biol 4:407-414. [ Links ]
Rommens CM and Kishore GM (2000) Exploiting the full potential of disease resistance genes for agricultural use. Curr Opin Biotechnol 11:120-125. [ Links ]
Ronald PC (1997) The molecular basis of disease resistance in rice. Plant Mol Biol 35:179-186. [ Links ]
Simmons G, Groenendijk J, Wijbrandi J, Reijans M, Groenen J, Diergaarde van der Lee T, Bleeker M, Onstenk J, De Both M, Haring M, Mes J, Cornelissen B, Zabeau M and Vos P (1998) Dissection of the fusarium I2 gene cluster in tomato reveals six homologs and one active gene copy. Plant Cell 10:1055-1068. [ Links ]
Song WY, Pi LY, Wang GL, Gardner J, Holsten T and Ronald PC (1997) Evolution of the rice Xa21 disease resistance genes family. Plant Cell 9:1279-1287. [ Links ]
Song WY, Wang GL, Chen LL, Kim HS, Pi LY, Holsten T, Gardner J, Wang B, Zhai WX, Zhu LH, Fauquet C and Ronald PC (1995) A receptor kinase-like protein encoded by the rice disease resistance gene Xa21. Science 270:1804-1806. [ Links ]
The Arabidopsis Genome Iniciative (2000) Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408:796-815. [ Links ]
Thomas CM, Jones DA, Parniske M, Harrison K, Balint-Kurti PJ, Hatzixanthis K and Jones JD (1997) Characterization of the tomato Cf-4 gene for resistance to Cladosporium fulvum identifies sequences that determine recognitional specificity in Cf-4 and Cf-9. Plant Cell 9:2209-2224. [ Links ]
van der Biezen EA and Jones JGD (1998) The NB-ARC domais: A novel signaling motif shared by plant resistance gene products and regulators of cell death in animals. Curr Biol 8:R226-R227. [ Links ]
van der Biezen EA, Freddie CT, Kahn K, Parker JE and Jones JD (2002) Arabidopsis RPP4 is a member of the RPP5 multigene family of TIR-NB-LRR genes and confers downy mildew resistance through multiple signaling components. Plant J 29:439-51. [ Links ]
van der Vossen EA, van der Voort JN, Kanyuka K, Bendahmane A, Sandbrink H, Baulcombe DC, Bakker J, Stiekema WJ and Klein-Lankhorst RM (2000) Homologues of a single resistance-gene cluster in potato confer resistance to distinct pathogens: A virus and a nematode. Plant J 23:567-576. [ Links ]
Wang ZX, Yano M, Yamanouchi U, Iwamoto M, Monna L, Hayasaka H, Katayose Y and Sasaki T (1999) The Pib gene for rice blast resistance belongs to the nucleotide binding and leucine-rich repeat class of plant disease resistance genes. Plant J 19:55-64. [ Links ]
Whithan S, McCormick S and Baker B (1996) The N gene of tobacco confers resistance to tobacco mosaic virus in transgenic tomato. Proc Natl Acad Sci USA 93:8776-81. [ Links ]
Xiao S, Ellwood S, Calis O, Patrick E, Li T, Coleman M and Turner JG (2001) Broad-spectrum mildew resistance in Arabidopsis thaliana mediated by RPW8. Science 291:118-20. [ Links ]
Yoshimura S, Yamanouchi U, Katayose Y, Toki S, Wang ZX, Kono I, Kurata N, Iwata N and Sasaki T (1998) Expression of Xa1, a bacterial blight-resistance gene in rice, is induced by bacterial inoculation. Proc Natl Acad Sci USA 95:1663-1668. [ Links ]
Send correspondence to
Ana Maria Benko-Iseppon
Universidade Federal de Pernambuco, Centro de Ciências Biológicas, Departamento de Genética, Laboratório de Genética e Biotecnologia Vegetal
Av. Prof. Moraes Rego s/ n.
50732-970 Recife, PE, Brazil
Received: May 28, 2004; Accepted: March 28, 2005.
Associate Editor: Marcio de Castro Silva Filho