Applying association mapping and genomic selection to the dissection of key traits in elite European wheat
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We show the application of association mapping and genomic selection for key breeding targets using a large panel of elite winter wheat varieties and a large volume of agronomic data.
The heightening urgency to increase wheat production in line with the needs of a growing population, and in the face of climatic uncertainty, mean new approaches, including association mapping (AM) and genomic selection (GS) need to be validated and applied in wheat breeding. Key adaptive responses are the cornerstone of regional breeding. There is evidence that new ideotypes for long-standing traits such as flowering time may be required. In order to detect targets for future marker-assisted improvement and validate the practical application of GS for wheat breeding we genotyped 376 elite wheat varieties with 3,046 DArT, single nucleotide polymorphism and gene markers and measured seven traits in replicated yield trials over 2 years in France, Germany and the UK. The scale of the phenotyping exceeds the breadth of previous AM and GS studies in these key economic wheat production regions of Northern Europe. Mixed-linear modelling (MLM) detected significant marker-trait associations across and within regions. Genomic prediction using elastic net gave low to high prediction accuracies depending on the trait, and could be experimentally increased by modifying the constituents of the training population (TP). We also tested the use of differentially penalised regression to integrate candidate gene and genome-wide markers to predict traits, demonstrating the validity and simplicity of this approach. Overall, our results suggest that whilst AM offers potential for application in both research and breeding, GS represents an exciting opportunity to select key traits, and that optimisation of the TP is crucial to its successful implementation.
KeywordsQuantitative Trait Locus Flowering Time Association Mapping Genomic Selection Single Nucleotide Polymorphism Marker
This work was supported by a Grant from the European Commission under the 7th Framework Programme for Research and Technological Development (FP7-212019). AB was funded by BB/I002561/1 from the UK Biotechnology and Biological Sciences Research Council whilst working on the manuscript. We thank the Editor and three anonymous reviewers for constructive comments for improving the manuscript.
Conflict of interest
The authors declare that they have no conflict of interest.
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