Abstract

Fusarium wilt (FW) and sterility mosaic diseases (SMD) are key biotic constraints to pigeonpea production. Occurrence of these two diseases in congenial conditions is reported to cause complete yield loss in susceptible pigeonpea cultivars. Various studies to elucidate genomic architecture of the two traits have revealed significant marker–trait associations for use in breeding programs. However, these DNA markers could not be used effectively in genomics-assisted breeding for developing FW and SMD resistant varieties primarily due to pathogen variability, location or background specificity, lesser phenotypic variance explained by the reported QTL and cost-inefficiency of the genotyping assays. Therefore, in the present study, a novel approach has been used to develop a diagnostic kit for identification of suitable FW and SMD resistant lines. This kit was developed with 10 markers each for FW and SMD resistance. Investigation of the diversity of these loci has shown the role of different alleles in different resistant genotypes. Two genes (C.cajan_03691 and C.cajan_18888) for FW resistance and four genes (C.cajan_07858, C.cajan_20995, C.cajan_21801 and C.cajan_17341) for SMD resistance have been identified. More importantly, we developed a customized and cost-effective Kompetitive allele-specific PCR genotyping assay for the identified genes in order to encourage their downstream applications in pigeonpea breeding programs. The diagnostic marker kit developed here will offer great strength to pigeonpea varietal development program, since the resistance against these two diseases is essentially required for nominating an improved line in varietal release pipeline.

Highlights

  • Since the inception of breeding, it has been defined as a combination of “Science” and “Art”

  • The genomic information on candidate regions associated with Fusarium wilt (FW) resistance and sterility mosaic diseases (SMD) resistance was assembled from the four different studies

  • The quantitative trait loci (QTL)-containing genomic regions as delineated by flanking SNPs in these studies were used for further analysis in order to capture corresponding complete sequence in the draft genome (Varshney et al 2012)

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Summary

Introduction

Since the inception of breeding, it has been defined as a combination of “Science” and “Art”. The “Science” component mainly includes understanding of genetics for desirable traits in a particular crop, whereas “Art” has relied on a breeder’s experience. Knowledge of genetics and the experience of breeder both remain essential to breed an improved cultivar/variety. A number of improved crop varieties resulting from plant breeding have contributed significantly to global food production. In spite of the significant progress in conventional breeding to date, it has been realized as a herculean task to match with the dietary demands of continuously growing population in changing climate. It is high time to focus on different components of the genetic gains/breeder’s equation [genetic gain (∆G) = heritability (h2) × phenotypic variability in population (σp) × selection intensity (i)/generation interval (L)] in almost all the crop improvement programs and transform

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