Extending the Marker × Environment Interaction Model for Genomic‐Enabled Prediction and Genome‐Wide Association Analysis in Durum Wheat

• Published in: Crop science 2016-09, Vol.56 (5), p.2193-2209
• Main Authors: Crossa, José, Campos, Gustavo, Maccaferri, Marco, Tuberosa, Roberto, Burgueño, J., Pérez‐Rodríguez, Paulino
• Format: Article
• Language: English
• ISSN: 0011-183X; 1435-0653
• DOI: 10.2135/cropsci2015.04.0260

The marker × environment interaction (M×E) genomic model can be used to generate predictions for untested individuals and identify genomic regions in which effects are stable across environments and others that show environmental specificity. The objectives of this study were (i) to extend the M×E model using priors that produce shrinkage and variable selection such as Bayesian ridge regression (BRR) and BayesB (BB), respectively, and (ii) to evaluate the genomic prediction accuracy of M×E, single‐environment, and across‐environment models using a multiparental durum wheat (Triticum turgidum L. spp. duram) population characterized for grain yield (GY), grain volume weight (GVW), 1000‐kernel weight (GWT), and heading date (HD) in four environments. Breeding value predictions were generated for two prediction problems: cross‐validation problem 1 (CV1) and cross‐validation problem 2 (CV2). In general, results showed that the M×E model performed better than the single‐environment and across‐environment models, in terms of minimizing the model residual variance, for both CV1 and CV2. The improved data‐fitting gain over the other models was more evident for GWT and HD (up to twofold differences) than to GY and GVW, which showed more complex genetic bases and smaller single‐marker effects. Considering the Bayesian models used, BB showed better overall prediction accuracy than BRR. As proof‐of‐concept for the M×E model, the major controllers of HD—Ppd and FT on chromosomes 2A, 2B, and 7A—showed stable effects across environments as well as environment‐specific effects. For GY, besides the regions on chromosomes 2B and 7A, additional chromosome regions with large marker effects were detected in all chromosome groups.