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Cassava is cultivated due to its drought tolerance and high carbohydrate-containing storage roots. The lack of uniformity and irregular shape of storage roots poses constraints on harvesting and post-harvest processing. Here, we phenotyped the Genetic gain and offspring (C1) populations from the International Institute of Tropical Agriculture (IITA) breeding program using image analysis of storage root photographs taken in the field. In the genome-wide association analysis (GWAS), we detected for most shape and size-related traits, QTL on chromosomes 1 and 12. In a previous study, we found the QTL on chromosome 12 to be associated with cassava mosaic disease (CMD) resistance. Because the root uniformity is important for breeding, we calculated the standard deviation (SD) of individual root measurements per clone. With SD measurements we identified new significant QTL for Perimeter, Feret and Aspect Ratio on chromosomes 6, 9 and 16. Predictive accuracies of root size and shape image-extracted traits were mostly higher than yield trait prediction accuracies. This study aimed to evaluate the feasibility of the image phenotyping protocol and assess GWAS and genomic prediction for size and shape image-extracted traits. The methodology described and the results are promising and open up the opportunity to apply high-throughput methods in cassava. [ABSTRACT FROM AUTHOR]

Brassica rapa studies towards metabolic variation have largely been focused on the profiling of the diversity of metabolic compounds in specific crop types or regional varieties, but none aimed to identify genes with regulatory function in metabolite composition. Here we followed a genetical genomics approach to identify regulatory genes for six biosynthetic pathways of health-related phytochemicals, i.e carotenoids, tocopherols, folates, glucosinolates, flavonoids and phenylpropanoids. Leaves from six weeks-old plants of a Brassica rapa doubled haploid population, consisting of 92 genotypes, were profiled for their secondary metabolite composition, using both targeted and LC-MS-based untargeted metabolomics approaches. Furthermore, the same population was profiled for transcript variation using a microarray containing EST sequences mainly derived from three Brassica species: B. napus, B. rapa and B. oleracea. The biochemical pathway analysis was based on the network analyses of both metabolite QTLs (mQTLs) and transcript QTLs (eQTLs). Co-localization of mQTLs and eQTLs lead to the identification of candidate regulatory genes involved in the biosynthesis of carotenoids, tocopherols and glucosinolates. We subsequently focused on the well-characterized glucosinolate pathway and revealed two hotspots of co-localization of eQTLs with mQTLs in linkage groups A03 and A09. Our results indicate that such a large-scale genetical genomics approach combining transcriptomics and metabolomics data can provide new insights into the genetic regulation of metabolite composition of Brassica vegetables. [ABSTRACT FROM AUTHOR]

With the recent advances in high throughput profiling techniques the amount of genetic and phenotypic data available has increased dramatically. Although many genetic diversity studies combine morphological and genetic data, metabolite profiling has yet to be integrated into these studies. For our study we selected 168 accessions representing the different morphotypes and geographic origins of Brassica rapa. Metabolite profiling was performed on all plants of this collection in the youngest expanded leaves, 5 weeks after transplanting and the same material was used for molecular marker profiling. During the same season a year later, 26 morphological characteristics were measured on plants that had been vernalized in the seedling stage. The number of groups and composition following a hierarchical clustering with molecular markers was highly correlated to the groups based on morphological traits ( r = 0.420) and metabolic profiles ( r = 0.476). To reveal the admixture levels in B. rapa, comparison with the results of the programme STRUCTURE was needed to obtain information on population substructure. To analyze 5546 metabolite (LC-MS) signals the groups identified with STRUCTURE were used for random forests classification. When comparing the random forests and STRUCTURE membership probabilities 86% of the accessions were allocated into the same subgroup. Our findings indicate that if extensive phenotypic data (metabolites) are available, classification based on this type of data is very comparable to genetic classification. These multivariate types of data and methodological approaches are valuable for the selection of accessions to study the genetics of selected traits and for genetic improvement programs, and additionally provide information on the evolution of the different morphotypes in B. rapa. [ABSTRACT FROM AUTHOR]

Control of gene expression is fundamental at every level of cell function. Promoter-proximal pausing and divergent transcription at promoters and enhancers, which are prominent features in animals, have only been studied in a handful of research experiments in plants. PRO-Seq analysis in cassava (Manihot esculenta) identified peaks of transcriptionally engaged RNA polymerase at both the 50 and 30 end of genes, consistent with paused or slowly moving Polymerase. In addition, we identified divergent transcription at intergenic sites. A full genome search for bi-directional transcription using an algorithm for enhancer detection developed in mammals (dREG) identified many intergenic regulatory element (IRE) candidates. These sites showed distinct patterns of methylation and nucleotide conservation based on genomic evolutionary rate profiling (GERP). SNPs within these IRE candidates explained significantly more variation in fitness and root composition than SNPs in chromosomal segments randomly ascertained from the same intergenic distribution, strongly suggesting a functional importance of these sites. Maize GRO-Seq data showed RNA polymerase occupancy at IREs consistent with patterns in cassava. Furthermore, these IREs in maize significantly overlapped with sites previously identified on the basis of open chromatin, histone marks, and methylation, and were enriched for reported eQTL. Our results suggest that bidirectional transcription can identify intergenic genomic regions in plants that play an important role in transcription regulation and whose identification has the potential to aid crop improvement. [ABSTRACT FROM AUTHOR]

Genotype × environment interaction (GEI) is one of the key factors affecting breeding value estimation accuracy for agronomic traits in plant breeding. Measures of GEI include fitting prediction models with various kernels to capture the variance resulting from GEI, and characterizing trials into megaenvironment (ME) clusters within which breeding values can be estimated to remove the main GEI effects. However, many of the current approaches require observations of common genotypes across all trials, which is unavailable in most breeding programs. Our study introduces two methods that can be implemented on unbalanced data to categorize trials into clusters, where both need a correlation matrix between trials: one estimated via a factor analytic (FA) model and another estimated via weather variables. The methods were tested using empirical barley (Hordeum vulgare L.) yield data in a commercial breeding program from 102 trials over 5 yr spread across multiple locations in Australia. Leave‐one‐year‐out cross‐validation achieved comparable predictive accuracies using either trials or clusters as the observed variable in GEI FA models (max. 0.45), which was higher than the accuracy achieved using the non‐GEI model (0.37). In the random cross‐validations, accuracies achieved within clusters (0.42–0.64) were mostly comparable with those achieved in the full population (0.62). In the within‐cluster validations, higher predictive accuracies were achieved when the training population was from the same cluster (mean 0.22) than outside of the cluster (mean 0.16). Our proposed methods of characterizing multienvironment trials into clusters provides a novel way to define training populations by reducing the variance resulting from GEI and could be implemented in any plant breeding program. Core Ideas: Genomic prediction implemented in breeding practiceMinimize variance caused by genotype × environment interactionclustering on multienvironment trials [ABSTRACT FROM AUTHOR]

Genomic selection can increase the rate of genetic gain in crops through accumulation of positive alleles and reduce phenotyping costs by shortening the breeding cycle time. We performed genomic prediction for resistance to wheat rusts in tetraploid wheat accessions using three cross-validation with the objective of predicting: (1) rust resistance when individuals are not tested in all environments/locations, (2) the performance of lines across years, and (3) adult plant resistance (APR) of lines with bivariate models. The rationale for the latter is that seedling assays are faster and could increase prediction accuracy for APR. Predictions were derived from adult plant and seedling responses for leaf rust (Lr), stem rust (Sr) and stripe rust (Yr) in a panel of 391 accessions grown across multiple years and locations and genotyped using 16,483 single nucleotide polymorphisms. Different Bayesian models and genomic best linear unbiased prediction yielded similar accuracies for all traits. Site and year prediction accuracies for Lr and Yr ranged between 0.56–0.71 for Lr and 0.51–0.56 for Yr. While prediction accuracy for Sr was variable across different sites, accuracies for Yr were similar across different years and sites. The changes in accuracies can reflect higher genotype × environment (G × E) interactions due to climate or pathogenic variation. The use of seedling assays in genomic prediction was underscored by significant positive genetic correlations between all stage resistance (ASR) and APR (Lr: 0.45, Sr: 0.65, Yr: 0.50). Incorporating seedling phenotypes in the bivariate genomic approach increased prediction accuracy for all three rust diseases. Our work suggests that the underlying plant-host response to pathogens in the field and greenhouse screens is genetically correlated, but likely highly polygenic and therefore difficult to detect at the individual gene level. Overall, genomic prediction accuracies were in the range suitable for selection in early generations of the breeding cycle. [ABSTRACT FROM AUTHOR]