Continued increases in genetic gain demonstrate the success of established public and private plant breeding programs. Nevertheless, in the last two decades, a growing body of modern technologies has been developed and now awaits efficient integration into traditional breeding pipelines. This integration offers attractive benefits, yet comes with the challenges of making modifications in established and operational systems, a recent example of which is rice breeding (Collard et al., 2019). Newly available technologies, genomics rapid cycling (Crossa et al., 2017), high throughput phenotyping (HTP, phenomics) (Montesinos-Lopez et al., 2017) and historical descriptions of environmental relatedness (enviromics) (Costa-Neto et al., 2020a,b; Resende et al., 2020; Rogers et al., 2021) are crucial to improving conventional breeding schemes and increasing genetic gain. Integrating these new technologies into routine breeding pipelines will support the delivery of cultivars with robust yields in the face of the expected unfavorable future environmental conditions caused by climate change and the consequently increased occurrence of biotic and abiotic stresses. Here, we briefly describe the use of these technologies and their implementation to provide cost-effective and time-saving approaches to plant breeding. We also give an overview of the interconnections between these techniques. Finally, we envision future perspectives to implement a more interconnected breeding approach that takes advantage of the so-called modern plant breeding triangle: integrating genomics, phenomics, and enviromics. Why Genomics for Improving Breeding? One of the most popular uses of genomics in breeding is the prediction of breeding values. Genomic selection (GS) reduces cycle time, increases the accuracy of estimated breeding values and improves selection accuracy. For instance, in maize, the effectiveness of GS has been proven for the case of bi-parental populations (Massman et al., 2013; Beyene et al., 2015; Vivek et al., 2017), as well as in multi-parental populations (Zhang et al., 2017). Its use has also been documented in species with long generation times such as trees (Grattapaglia et al., 2018) and dairy cattle breeding, where the reduction of the breeding cycle has increased the response to selection in comparison with the progeny testing system (Garcia-Ruiz et al., 2016). Genomic selection has been implemented in many crops, including wheat, chickpea, cassava and rice (Roorkiwal et al., 2016; Crossa et al., 2017; Wolfe et al., 2017; Huang et al., 2019), and the number of programs that are moving from “conventional” to GS is growing. Results in wheat show that genomic predictions used early in the breeding cycle led to a substantial increase in performance in later generations (Bonnett et al., 2021 this issue). Defining Foundational Core Parents for Genomic Selection-Assisted Breeding In genomic selection, the optimization of the training set composition is an important topic because training and testing sets should be genetically related in such a way that the genetic diversity present in the testing set could be covered and captured by the diversity in the training set. Breeding programs must start forming initial foundational core parents (training populations) that represent the genetic diversity found in the current progeny and conform to the testing population(s) to the greatest extent possible (Hickey et al., 2012). These foundational parents should be extensively phenotyped in different target populations of environments and genotyped with high-density marker systems. These training sets of foundation parents will be able to produce a model with a high accuracy for current highly selected progenies (Zhang et al., 2017).
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Nov 16, 2021
Karl W Broman 
Open Access
