alexa Identifcation Of Resistance Gene Analogs In Cabbage By PCR-SSCP Analysis
ISSN: 0974-276X

Journal of Proteomics & Bioinformatics
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World Congress on Biotechnology
21-23 March, 2011

Kaunain Roohie R and Umesha S
Track 4: JPB
DOI: 10.4172/jpb.1000240
Abstract
The class of R-genes encoding a Nucleotide Binding Site (NBS) and/or a Leucine Rich Repeat (LRR) region is responsible for a mechanism of resistance to pathogens in many crops. The use of degenerate primers designed on the conserved domains would be a fast techinque for the identification of candidate R-genes. The Resistance Gene Analogs (RGAs) of the NBS-LRR class from the genomic DNA of cabbage will be isolated using degenerrate primers . PCR-generated fragments arising from a multi-gene family will cloned into a plasmid vector. Followed by the fingerprinting using SSCP-analysis of the inserts in order to find out unique clones before sequencing. Specific-RGAs will be characterised by conformational polymorphism (SSCP analysis) in a panel of cabbge genotypes carrying different levels of resistance. The expression of R-genes in the presence or absence of Black rot pathogen will also be taken up in the present study.
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