January 14-18, 2006
Town & Country Convention Center
San Diego, CA
Prasanna Ramachandra Bhat1,2 , Krishnakumar V1 , Prasad Suresh Hendre1 , Rajendrakumar P1 , Ramesh Kumar Aggarwal1
Recent studies have shown that R-genes conferring resistance to diverse pathogens in different plant species share a number of common functional motifs and are frequently clustered in the genome. This considerable conservation at the DNA sequence/protein level in R-genes has led to the development of novel PCR-based molecular approaches to isolate putative resistance gene analogues (RGAs) from new plant sources with considerable ease. We have successfully used one such approach to amplify putative RGAs from Coffea and four related endemic Psilanthus taxa with degenerate primer pairs designed from conserved P-LOOP and GLPL region of NBS-LRR type resistance gene. We tested both the total genomic DNA, as well as cDNA as templates in coffee and only genomic DNA for the four related taxa. The PCR-amplified products of expected size range of 500bp were cloned in to pMOS plasmid vector. The cloned fragments were amplified from the recombinant plasmid DNA using M13 universal primers and were sequenced for both strands on an automated DNA sequencer ABI3700 using fluorescencedideoxy terminator chemistry. The sequences were partially characterized by BLASTn homology searches. Of the 434 sequences, thus analyzed, there were twenty-seven sequences that had all the characteristic features of the known NBS-LRR type of R-genes. Of these 27 putative RGAs, 24 had complete uninterrupted reading frame, while remaining 3 sequences showed one or more stop codons. The sequence comparisons with known reference RGAs of coffee and other plant species revealed considerable variability in the putative RGAs amplified in the study, especially for those from related, wild Psilanthus taxa. The data thus suggest the potential of the secondary genepool as donors of possible resistance genes to the present day cultivated species of coffee.