Enviromics in breeding: applications and perspectives on envirotypic-assisted selection.

KEY MESSAGE: We propose the application of enviromics to breeding practice, by which the similarity among sites assessed on an "omics" scale of environmental attributes drives the prediction of unobserved genotype performances. Genotype by environment interaction (GEI) studies in plant breeding have focused mainly on estimating genetic parameters over a limited number of experimental trials. However, recent geographic information system (GIS) techniques have opened new frontiers for better understanding and dealing with GEI. These advances allow increasing selection accuracy across all sites of interest, including those where experimental trials have not yet been deployed. Here, we introduce the term enviromics, within an envirotypic-assisted breeding framework. In summary, likewise genotypes at DNA markers, any particular site is characterized by a set of "envirotypes" at multiple "enviromic" markers corresponding to environmental variables that may interact with the genetic background, thus providing informative breeding re-rankings for optimized decisions over different environments. Based on simulated data, we illustrate an index-based enviromics method (the "GIS-GEI") which, due to its higher granular resolution than standard methods, allows for: (1) accurate matching of sites to their most appropriate genotypes; (2) better definition of breeding areas that have high genetic correlation to ensure selection gains across environments; and (3) efficient determination of the best sites to carry out experiments for further analyses. Environmental scenarios can also be optimized for productivity improvement and genetic resources management, especially in the current outlook of dynamic climate change. Envirotyping provides a new class of markers for genetic studies, which are fairly inexpensive, increasingly available and transferable across species. We envision a promising future for the integration of enviromics approaches into plant breeding when coupled with next-generation genotyping/phenotyping and powerful statistical modeling of genetic diversity.

Genome-Wide Association and Regional Heritability Mapping of Plant Architecture, Lodging and Productivity in Phaseolus vulgaris.

The availability of high-density molecular markers in common bean has allowed to explore the genetic basis of important complex agronomic traits with increased resolution. Genome-Wide Association Studies (GWAS) and Regional Heritability Mapping (RHM) are two analytical approaches for the detection of genetic variants. We carried out GWAS and RHM for plant architecture, lodging and productivity across two important growing environments in Brazil in a germplasm of 188 common bean varieties using DArTseq genotyping strategies. The coefficient of determination of G × E interaction (c2int ) was equal to 17, 21 and 41%, respectively for the traits architecture, lodging, and productivity. Trait heritabilities were estimated at 0.81 (architecture), 0.79 (lodging) and 0.43 (productivity), and total genomic heritability accounted for large proportions (72% to ≈100%) of trait heritability. At the same probability threshold, three marker-trait associations were detected using GWAS, while RHM detected eight QTL encompassing 145 markers along five chromosomes. The proportion of genomic heritability explained by RHM was considerably higher (35.48 to 58.02) than that explained by GWAS (28.39 to 30.37). In general, RHM accounted for larger fractions of the additive genetic variance being captured by markers effects inside the defined regions. Nevertheless, a considerable proportion of the heritability is still missing (∼42% to ∼64%), probably due to LD between markers and genes and/or rare allele variants not sampled. RHM in autogamous species had the potential to identify larger-effect QTL combining allelic variants that could be effectively incorporated into whole-genome prediction models and tracked through breeding generations using marker-assisted selection.

Genomic growth curves of an outbred pig population.

In the current post-genomic era, the genetic basis of pig growth can be understood by assessing SNP marker effects and genomic breeding values (GEBV) based on estimates of these growth curve parameters as phenotypes. Although various statistical methods, such as random regression (RR-BLUP) and Bayesian LASSO (BL), have been applied to genomic selection (GS), none of these has yet been used in a growth curve approach. In this work, we compared the accuracies of RR-BLUP and BL using empirical weight-age data from an outbred F2 (Brazilian Piau X commercial) population. The phenotypes were determined by parameter estimates using a nonlinear logistic regression model and the halothane gene was considered as a marker for evaluating the assumptions of the GS methods in relation to the genetic variation explained by each locus. BL yielded more accurate values for all of the phenotypes evaluated and was used to estimate SNP effects and GEBV vectors. The latter allowed the construction of genomic growth curves, which showed substantial genetic discrimination among animals in the final growth phase. The SNP effect estimates allowed identification of the most relevant markers for each phenotype, the positions of which were coincident with reported QTL regions for growth traits.