Abstract

BackgroundMolecular marker-assisted breeding provides an efficient tool to develop improved crop varieties. A major challenge for the broad application of markers in marker-assisted selection is that the marker phenotypes must match plant phenotypes in a wide range of breeding germplasm. In this study, we used the legume crop species Lupinus angustifolius (lupin) to demonstrate the utility of whole genome sequencing and re-sequencing on the development of diagnostic markers for molecular plant breeding.ResultsNine lupin cultivars released in Australia from 1973 to 2007 were subjected to whole genome re-sequencing. The re-sequencing data together with the reference genome sequence data were used in marker development, which revealed 180,596 to 795,735 SNP markers from pairwise comparisons among the cultivars. A total of 207,887 markers were anchored on the lupin genetic linkage map. Marker mining obtained an average of 387 SNP markers and 87 InDel markers for each of the 24 genome sequence assembly scaffolds bearing markers linked to 11 genes of agronomic interest. Using the R gene PhtjR conferring resistance to phomopsis stem blight disease as a test case, we discovered 17 candidate diagnostic markers by genotyping and selecting markers on a genetic linkage map. A further 243 candidate diagnostic markers were discovered by marker mining on a scaffold bearing non-diagnostic markers linked to the PhtjR gene. Nine out from the ten tested candidate diagnostic markers were confirmed as truly diagnostic on a broad range of commercial cultivars. Markers developed using these strategies meet the requirements for broad application in molecular plant breeding.ConclusionsWe demonstrated that low-cost genome sequencing and re-sequencing data were sufficient and very effective in the development of diagnostic markers for marker-assisted selection. The strategies used in this study may be applied to any trait or plant species. Whole genome sequencing and re-sequencing provides a powerful tool to overcome current limitations in molecular plant breeding, which will enable plant breeders to precisely pyramid favourable genes to develop super crop varieties to meet future food demands.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1878-5) contains supplementary material, which is available to authorized users.

Highlights

  • Molecular marker-assisted breeding provides an efficient tool to develop improved crop varieties

  • The total length of scaffold span for each cultivar ranged from 485 Mbp to 513 Mbp, approximately 90 % of the length of the reference genome assembly based on cultivar Tanjil [38]

  • The results in this study have demonstrated that low coverage genome sequencing and re-sequencing data were sufficient and very effective on marker development in molecular plant breeding

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Summary

Introduction

Molecular marker-assisted breeding provides an efficient tool to develop improved crop varieties. We used the legume crop species Lupinus angustifolius (lupin) to demonstrate the utility of whole genome sequencing and re-sequencing on the development of diagnostic markers for molecular plant breeding. The success of plant breeding and selection has relied on phenotypic measurements and breeder experience. The advent of molecular biotechnology has progressively provided improved tools for precision plant breeding for genetic improvement. The concept of marker-assisted selection (MAS) in plant breeding was proposed in the 1980s [1], and has the potential to vastly enhance the efficiency of genetic improvement [2, 3]. In the last 30 years, molecular markers have been gradually applied to assist plant breeding of agricultural crops. Most of the thousands of publications with the terms “markerassisted selection”, “quantitative trait loci (QTLs)” or “molecular markers” have failed to show any impact in plant breeding [3,4,5]

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