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Open AccessResearch article

Detection and validation of single feature polymorphisms in cowpea (Vigna unguiculata L. Walp) using a soybean genome array

Sayan Das* 1,2 email, Prasanna R Bhat* 1 email, Chinta Sudhakar1,3 email, Jeffrey D Ehlers1 email, Steve Wanamaker1 email, Philip A Roberts2 email, Xinping Cui4 email and Timothy J Close1 email

1Department of Botany and Plant Sciences, University of California, Riverside, CA 92521 USA

2Department of Nematology, University of California, Riverside, CA 92521 USA

3Department of Botany and Biotechnology, Sri Krishnadevaraya University, Anantapur, 515 003 India

4Department of Statistics, University of California, Riverside, CA 92521 USA

author email corresponding author email* Contributed equally

BMC Genomics 2008, 9:107doi:10.1186/1471-2164-9-107

Published: 28 February 2008

Abstract

Background

Cowpea (Vigna unguiculata L. Walp) is an important food and fodder legume of the semiarid tropics and subtropics worldwide, especially in sub-Saharan Africa. High density genetic linkage maps are needed for marker assisted breeding but are not available for cowpea. A single feature polymorphism (SFP) is a microarray-based marker which can be used for high throughput genotyping and high density mapping.

Results

Here we report detection and validation of SFPs in cowpea using a readily available soybean (Glycine max) genome array. Robustified projection pursuit (RPP) was used for statistical analysis using RNA as a surrogate for DNA. Using a 15% outlying score cut-off, 1058 potential SFPs were enumerated between two parents of a recombinant inbred line (RIL) population segregating for several important traits including drought tolerance, Fusarium and brown blotch resistance, grain size and photoperiod sensitivity. Sequencing of 25 putative polymorphism-containing amplicons yielded a SFP probe set validation rate of 68%.

Conclusion

We conclude that the Affymetrix soybean genome array is a satisfactory platform for identification of some 1000's of SFPs for cowpea. This study provides an example of extension of genomic resources from a well supported species to an orphan crop. Presumably, other legume systems are similarly tractable to SFP marker development using existing legume array resources.


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