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Bandillo, N.

Publications and source records attributed to Bandillo, N..

16 recordsLinked to original sources

Environmentally-mediated yield effects of vernalization and photoperiod alleles in historic winter wheat trials

In common wheat (Triticum aestivum L.), variation at the Vrn1 and Ppd1 loci changes plant phenology, resulting in differential adaptation useful to breeders. Because the effects of phenology on grain yield are conditional on environmental factors, the incorporation of markers for Vrn1 and Ppd1 alleles into breeding approaches has proven difficult. Historic phenotypic, genotypic, and environmental data can provide insight into the relationship between major phenology alleles and grain yield as mediated by environmental variables. Analyses of eight years of breeding trials (1,038 lines at 219 site-years) determined that weak vrn1 alleles and Ppd1 insensitivity alleles have variable effects. These effects change depending on an environment's winter temperature and latitude, respectively, but the environmentally-driven changes in effect of vrn1 alleles are much more variable than effects of Ppd1 alleles. Mediation analyses showed phenologically-dependent environmental variables are one mechanism through which phenological changes created by vrn1 and Ppd1 variants alter yield across multiple developmental stages. Environmentally-driven relationships between flowering time and yield were modeled to estimate yield allele effects as a function of effects on phenology and environmental variables. Weak winter alleles at vrn1 may play a stabilizing role on yield, due to the correlation of winter conditions that drive larger effects with later-season warm temperatures that penalize later maturity. A better mechanistic understanding of how these loci drive environment-specific yield effects may facilitate utilization of markers for these alleles and improve predictive modeling of yield.

genetics↗

Reaction Norm Modeling of High-Dimensional Genomic and Environmental Data Improves Prediction Accuracy in Winter Wheat

Genomic prediction models that account genotype-by-environment (GxE) have the potential to accelerate the rate of genetic gain for yield and agronomic performance, yet relatively few studies have applied GxE prediction in public soft red winter wheat (Triticum aestivum) breeding programs. In this study, we extended a reaction norm-based genomic prediction framework by integrating weather-based environmental covariates to more effectively capture genotype- environment interactions. Key agronomic traits, including seed yield, plant height, test weight, and heading date, were evaluated across 33 environments (location-year) using over 3,200 breeding lines from the North Carolina State University small grains breeding program. Multiple genomic prediction models were compared using several cross-validation (CV) schemes representing common breeding scenarios. Across traits, the reaction norm M5 model, which incorporates both GxE and genotype-by-environmental covariate interactions (GxO), achieved the highest prediction accuracy (PA) in CV2 (predicting incomplete field trials) and CV1 for yield and test weight (predicting new lines). The highest PA was observed for test weight under CV2 (0.54) and for yield under CV1 (0.41). Under CV0 (predicting new environments), the M3 model incorporating GxE produced highest PA across traits, with the greatest accuracy for plant height (0.45), although differences among M2, M3, and M4 were small. Prediction under CV00 (predicting new lines in new environments) remained more challenging, with PA values 0.10 - 0.20 across traits. Overall, our results demonstrate that integrating environmental covariates into genomic prediction models can improve predictive performance across diverse wheat-growing environments in North Carolina, supporting their utility for applied breeding efforts. CORE IDEASO_LIIntegrating genotype-by-environment (GxE) interactions with environmental covariates improves prediction accuracy across environments. C_LIO_LIModel performance varies by prediction scenario, with different approaches performing best for new lines, incomplete trials, or new environments. C_LIO_LIPrediction of new lines in new environments remains challenging. C_LI PLAIN LANGUAGE SUMMARYThis study explores how adding environmental information to genomic prediction models can improve prediction accuracy in a public winter wheat breeding program. Using data from multi-environment trials conducted across diverse conditions in North Carolina, we evaluated statistical models that capture how different wheat lines respond to changing environments. By incorporating weather data, we improved the ability to predict performance across locations and years. These findings provide practical insights for refining selection strategies and accelerating genetic gain in wheat breeding.

genetics↗

Genomic and Transcriptomic Basis of Salinity Tolerance in Dry Pea

Salinity is a major crop production constraint in dry pea (Pisum sativum L.), making the development of salt-tolerant varieties essential to improve crop productivity and land-use efficiency. The genetic mechanisms of salt tolerance in dry pea is largely unknown, and research on salt-tolerant genes is limited. In this study, we established comprehensive genomic and transcriptomic resources, along with a robust screening protocol, to dissect the genetic basis of salinity tolerance using two germplasm sets: the USDA pea diversity panel, consisting of approximately 200 globally sourced accessions, and a set of 300 modern elite lines from the NDSU Pulse Crops Breeding Program. Genetic variation for the salinity response was assessed based on ten phenotypic traits, with root dry weight, shoot dry weight, and specific root length identified as key indicators based on their heritability. Genome-wide association mapping uncovered significant genomic regions and several candidate genes linked to salt stress, with the strongest association found on chromosome 6. Overlapping QTL signals across traits suggest a shared genetic architecture underlying salinity tolerance. Field-based transcriptomic analysis further identified five putative genes involved in salinity response conserved across multiple crop species. Notably, Psat5g000800, encoding a glycosyl hydrolase gene, was markedly upregulated under salinity stress. These findings highlight the complex, multi-gene regulatory nature of salinity tolerance in dry pea and underscore the importance of functional validation of candidate genes. This study provides key insights and practical tools to support breeding efforts aimed at improving salt tolerance in dry pea.

genetics↗

High-Throughput Phenotyping of Seed Quality Traits Using Imaging and Deep Learning in Dry Pea

Seed traits, such as seed color and seed size, directly impact seed quality, affecting the marketability and value of dry peas [1]. Assessing seed quality is integral to a plant breeding programs to ensure optimal seed standards. This research introduced a phenotyping tool to assess seed quality traits specifically tailored for pulse crops, which integrates image processing with cutting-edge deep learning models. The proposed method is designed for automation, seamlessly processing a sequence of images while minimizing human intervention. The pipeline standardized red-green-blue (RGB) images captured from a color light box and used deep learning models to segment and detect seed features. Our method extracted up to 86 distinct seed characteristics, ranging from basic size metrics to intricate texture details and color nuances. Compared to traditional methods, our pipeline demonstrated a 95 percent similarity in seed quality assessment and increased time efficiency (from 2 weeks to 30 minutes for processing time). Specifically, we observed an improvement in the accuracy of seed trait identification by simply using an RGB value instead of a categorical, non-standard description, which allowed for an increase in the range of detectable seed quality characteristics. By integrating conventional image processing techniques with foundational deep learning models, this approach emerges as a pivotal instrument in pulse breeding programs, guaranteeing the maintenance of superior seed quality standards.

plant biology↗

Multi-trait multi-environment genomic prediction of preliminary yield trials in pulse crops

Phenotypic selection in preliminary yield trials (PYT) is challenged by limited seeds, resulting in trials with few replications and environments. The emergence of multi-trait multi-environment enabled genomic prediction (MTME-GP) offers opportunity for enhancing prediction accuracy and genetic gain across multiple traits and diverse environments. Using a set of 300 advanced breeding lines in the North Dakota State University (NDSU) pulse crop breeding program, we assessed the efficiency of a MTME-GP model for improving seed yield and protein content in field peas in stress and non-stress environments. MTME-GP significantly improved predictive ability, improving up to 2.5-fold, particularly when a significant number of genotypes overlapped across environments. Heritability of the training environments contributed significantly to the overall prediction of the model. Average predictive ability ranged from 3 to 7-folds when environments with low heritability were excluded from the training set. Overall, the Reproducing Kernel Hilbert Spaces (RKHS) model consistently resulted in improved predictive ability across all breeding scenarios considered in our study. Our results lay the groundwork for further exploration, including integration of diverse traits, incorporation of deep learning techniques, and the utilization of multi-omics data in predictive modeling. Core ideasO_LIPhenotypic selection in PYT is challenged by limited seeds, resulting to few replications and environments. C_LIO_LIMTME-GP offers opportunity for enhancing prediction accuracy of multi-trait and diverse environments in PYT. C_LIO_LIMTME-GP enhances prediction by up to 2.5-fold, especially with numerous overlapping genotypes in various tested environments. C_LIO_LIRKHS MTME-GP models, excels in low-heritability, negatively correlated traits, like drought-affected conditions. C_LI

genomics↗

Effective Population Size in Field Pea

BackgroundEffective population size (Ne) is a pivotal parameter in population genetics as it can provide information on the rate of inbreeding and the contemporary status of genetic diversity in breeding populations. The population with smaller Ne can lead to faster inbreeding, with little potential for genetic gain making selections ineffective. The importance of Ne has become increasingly recognized in plant breeding, which can help breeders monitor and enhance the genetic variability or redesign their selection protocols. Here, we present the first Ne estimates based on linkage disequilibrium (LD) in the pea genome. ResultsWe calculated and compared Ne using SNP markers from North Dakota State University (NDSU) modern breeding lines and United States Department of Agriculture (USDA) diversity panel. The extent of LD was highly variable not only between populations but also among different regions and chromosomes of the genome. Overall, NDSU had a higher and longer-range LD than the USDA that could extend up to 500Kb, with a genome-wide average r2 of 0.57 (vs 0.34), likely due to its lower recombination rates and the selection background. The estimated Ne for the USDA was nearly three-fold higher (Ne = 174) than NDSU (Ne = 64), which can be confounded by a high degree of population structure due to the selfing nature of pea. ConclusionsOur results provided insights into the genetic diversity of the germplasm studied, which can guide plant breeders to actively monitor Ne in successive cycles of breeding to sustain viability of the breeding efforts in the long term.

genetics↗

Genomic-inferred cross-selection metrics for multi-trait improvement in a recurrent selection breeding program

The major drawback to the implementation of genomic selection in a breeding program is the reduction of additive genetic variance in the long term, primarily due to the Bulmer effect. Increasing genetic gain and retaining additive genetic variance requires optimizing the trade-off between the two competing factors. Our approach integrated index selection in the genomic infer cross-selection (GCS) methods. With this strategy, we identified optimal crosses that simultaneously maximize progeny performance and maintain genetic variance for multiple traits. Using a stochastic simulated recurrent breeding program over a 40-year period, we evaluated different GCS metrics with other factors, such as the number of parents, crosses, and progenies per cross, that influence genetic gain in a breeding program. Across all breeding scenarios, the posterior mean-variance consistently enhances genetic gain when compared to other metrics such as the usefulness criterion, optimal haploid value, mean genomic estimated breeding value, and mean index selection value of the superior parents. In addition, we provide a detailed strategy to optimize the number of parents, crosses, and progenies per cross that maximizes short- and long-term genetic gain in a breeding program.

genetics↗

A greenhouse-based high-throughput phenotyping platform for identification and genetic dissection of resistance to Aphanomyces root rot in field pea

Aphanomyces root rot (ARR) is a devastating disease in field pea (Pisum sativum L.) that can cause up to 100% crop failure. Assessment of ARR resistance can be a rigorous, costly, time-demanding activity that is relatively low-throughput and prone to human errors. These limits the ability to effectively and efficiently phenotype the disease symptoms arising from ARR infection, which remains a perennial bottleneck to the successful evaluation and incorporation of disease resistance into new cultivars. In this study, we developed a greenhouse-based high throughput phenotyping (HTP) platform that moves along the rails above the greenhouse benches and captures the visual symptoms caused by Aphanomyces euteiches in field pea. We pilot tested this platform alongside with conventional visual scoring in five experimental trials under greenhouse conditions, assaying over 12,600 single plants. Precision estimated through broad-sense heritability (H2) was consistently higher for the HTP-indices (H2 Exg =0.86) than the traditional visual scores (H2 DSI=0.59), potentially increasing the power of genetic mapping. We genetically dissected variation for ARR resistance using the HTP-indices, and identified a total of 260 associated single nucleotide polymorphism (SNP) through genome-wide association (GWA) mapping. The number of associated SNP for HTP-indices was consistently higher with some SNP overlapped to the associated SNP identified using the visual scores. We identified numerous small-effect QTLs, with the most significant SNP explaining about 5 to 9% of the phenotypic variance per index, and identified previously mapped genes known to be involved in the biological pathways that trigger immunity against ARR, including Psat5g280480, Psat5g282800, Psat5g282880, and Psat2g167800. We also identified a few novel QTLs with small-effect sizes that may be worthy of validation in the future. The newly identified QTLs and underlying genes, along with genotypes with promising resistance identified in this study, can be useful for improving a long-term, durable resistance to ARR.

pathology↗

Genomic selection performs as effectively as phenotypic selection for increasing seed yield in soybean

Increasing the rate of genetic gain for seed yield remains the primary breeding objective in both public and private soybean breeding programs. Genomic selection (GS) has the potential to accelerate the rate of genetic gain for soybean seed yield. To date, limited studies have empirically validated accuracy of GS and compared to phenotypic selection (PS), and none has been done for soybean breeding. This study conducted the first empirical validation of GS for increasing seed yield using over 1,500 lines and over 7 years (2010-2016) of replicated experiments in the University of Nebraska soybean breeding program. The study was designed to capture the varying genetic relatedness of the training population to three validation sets: two large bi-parental populations (TBP-1 and TBP-2), and a large validation set comprised of 457 pre-selected advanced lines derived from 45 bi-parental populations in the variety development program (TMP). We found that prediction accuracy (0.54) from our validation experiments was competitive with what we obtained from a series of cross-validation experiments (0.64). Both GS and PS were more effective for increasing population mean performance with similar realized gain but significantly greater than random selection (RS). We found a selection advantage of GS over PS where higher genetic gain and identification of top-performing lines was maximized at higher selection stringency from 10 to 20% selected proportion. GS led to at least 2% increase in the mean genetic similarity vs. PS and RS, potentially causing a minimal loss of genetic diversity. We showed that loss of genetic variance in the GS set was presumably due to a significant shift on allelic frequencies towards the extremes. Across all loci, an average increase of 0.04 in allelic frequency in the GS set was observed after selection, which is about 5% higher than the base population when no selection was made. Overall, we demonstrate that GS performed as effectively as PS, and the implementation of GS in a public soybean breeding program should be warranted mainly for reducing breeding cycle time and lowering cost per unit gain.

genetics↗

Multi-trait genomic prediction improves selection accuracy for enhancing seed mineral concentrations in pea (Pisum sativum L.)

The superiority of multi-trait genomic selection (MT-GS) over univariate genomic selection (UNI-GS) can be improved by redesigning the phenotyping strategy. In this study, we used about 300 advanced breeding lines from North Dakota State University (NDSU) pulse breeding program and about 200 USDA accessions evaluated for ten nutritional traits to assess the efficiency of sparse testing in MT-GS. Our results showed that sparse phenotyping using MT-GS consistently outperformed UNI-GS when compared to partially balanced phenotyping using MT-GS. This strategy can be further extended to multi-environment multi-trait GS to improve prediction performance and reduce the cost of phenotyping and time-consuming data collection process. Given that MT-GS relies on borrowing information from genetically correlated traits and relatives, consideration should be given to trait combinations in the training and prediction sets to improve model parameters estimate and ultimately prediction performance. Our results point to heritability and genetic correlation between traits as possible parameters to achieve this objective.

genetics↗

Harnessing genetic diversity in the USDA pea (Pisum sativum L.) germplasm collection through genomic prediction

Phenotypic evaluation and efficient utilization of germplasm collections can be time-intensive, laborious, and expensive. However, with the plummeting costs of next-generation sequencing and the addition of genomic selection to the plant breeders toolbox, we now can more efficiently tap the genetic diversity within large germplasm collections. In this study, we applied and evaluated genomic selections potential to a set of 482 pea accessions - genotyped with 30,600 single nucleotide polymorphic (SNP) markers and phenotyped for seed yield and yield-related components - for enhancing selection of accessions from the USDA Pea Germplasm Collection. Genomic prediction models and several factors affecting predictive ability were evaluated in a series of cross-validation schemes across complex traits. Different genomic prediction models gave similar results, with predictive ability across traits ranging from 0.23 to 0.60, with no model working best across all traits. Increasing the training population size improved the predictive ability of most traits, including seed yield. Predictive abilities increased and reached a plateau with increasing number of markers presumably due to extensive linkage disequilibrium in the pea genome. Accounting for population structure effects did not significantly boost predictive ability, but we observed a slight improvement in seed yield. By applying the best genomic prediction model (e.g., RR-BLUP), we then examined the distribution of genotyped but nonphenotyped accessions and the reliability of genomic estimated breeding values (GEBV). The distribution of GEBV suggested that none of the nonphenotyped accessions were expected to perform outside the range of the phenotyped accessions. Desirable breeding values with higher reliability can be used to identify and screen favorable germplasm accessions. Expanding the training set and incorporating additional orthogonal information (e.g., transcriptomics, proteomics, metabolomics, physiological traits, etc.) into the genomic prediction framework could enhance prediction accuracy.

genomics↗

Phenotyping stomatal closure by thermal imaging for GWAS and TWAS of water use efficiency-related genes

Stomata allow CO2 uptake by leaves for photosynthetic assimilation at the cost of water vapor loss to the atmosphere. The opening and closing of stomata in response to fluctuations in light intensity regulate CO2 and water fluxes and are essential to maintenance of water-use efficiency (WUE). However, little is known about the genetic basis for natural variation in stomatal movement, especially in C4 crops. This is partly because the stomatal response to a change in light intensity is difficult to measure at the scale required for association studies. High-throughput thermal imaging was used to bypass the phenotyping bottleneck and assess 10 traits describing stomatal conductance (gs) before, during and after a stepwise decrease in light intensity for a diversity panel of 659 sorghum accessions. Results from thermal imaging significantly correlated with photosynthetic gas-exchange measurements. gs traits varied substantially across the population and were moderately heritable (h2 up to 0.72). An integrated genome-wide and transcriptome-wide association study (GWAS/TWAS) identified candidate genes putatively driving variation in stomatal conductance traits. Of the 239 unique candidate genes identified with greatest confidence, 77 were orthologs of Arabidopsis genes related to functions implicated in WUE, including stomatal opening/closing (24 genes), stomatal/epidermal cell development (35 genes), leaf/vasculature development (12 genes), or chlorophyll metabolism/photosynthesis (8 genes). These findings demonstrate an approach to finding genotype-to-phenotype relationships for a challenging trait as well as candidate genes for further investigation of the genetic basis of WUE in a model C4 grass for bioenergy, food, and forage production. One sentence summaryRapid phenotyping of 659 accessions of Sorghum bicolor revealed heritable stomatal responses to a decrease in light. GWAS/TWAS was used to identify candidate genes influencing traits important to WUE.

plant biology↗

Comparative evolutionary analysis and prediction of deleterious mutation patterns between sorghum and maize

Sorghum and maize share a close evolutionary history that can be explored through comparative genomics. To perform a large-scale comparison of the genomic variation between these two species, we analyzed 13 million variants identified from whole genome resequencing of 468 sorghum lines together with 25 million variants previously identified in 1,218 maize lines. Deleterious mutations in both species were prevalent in pericentromeric regions, enriched in non-syntenic genes, and present at low allele frequencies. A comparison of deleterious burden between sorghum and maize revealed that sorghum, in contrast to maize, departed from the \"domestication cost\" hypothesis that predicts a higher deleterious burden among domesticates compared to wild lines. Additionally, sorghum and maize population genetic summary statistics were used to predict a gene deleterious index with an accuracy higher than 0.5. This research represents a key step towards understanding the evolutionary dynamics of deleterious variants in sorghum and provides a comparative genomics framework to start prioritizing them for removal through genome editing and breeding.

genomics↗

Metabolome-scale genome-wide association studies reveal chemical diversity and genetic control of maize specialized metabolites

One Sentence SummaryHPLC-MS metabolite profiling of maize seedlings, in combination with genome-wide association studies, identifies numerous quantitative trait loci that influence the accumulation of foliar metabolites.\n\nAbstractCultivated maize (Zea mays) retains much of the genetic and metabolic diversity of its wild ancestors. Non-targeted HPLC-MS metabolomics using a diverse panel of 264 maize inbred lines identified a bimodal distribution in the prevalence of foliar metabolites. Although 15% of the detected mass features were present in >90% of the inbred lines, the majority were found in <50% of the samples. Whereas leaf bases and tips were differentiated primarily by flavonoid abundance, maize varieties (stiff-stalk, non-stiff-stalk, tropical, sweet corn, and popcorn) were differentiated predominantly by benzoxazinoid metabolites. Genome-wide association studies (GWAS), performed for 3,991 mass features from the leaf tips and leaf bases, showed that 90% have multiple significantly associated loci scattered across the genome. Several quantitative trait locus hotspots in the maize genome regulate the abundance of multiple, often metabolically related mass features. The utility of maize metabolite GWAS was demonstrated by confirming known benzoxazinoid biosynthesis genes, as well as by mapping isomeric variation in the accumulation of phenylpropanoid hydroxycitric acid esters to a single linkage block in a citrate synthase-like gene. Similar to gene expression databases, this metabolomic GWAS dataset constitutes an important public resource for linking maize metabolites with biosynthetic and regulatory genes.

genetics↗

Transcriptome-wide association supplements genome-wide association in Zea mays

Modern improvement of complex traits in agricultural species relies on successful associations of heritable molecular variation with observable phenotypes. Historically, this pursuit has primarily been based on easily measurable genetic markers. The recent advent of new technologies allows assaying and quantifying biological intermediates (hereafter endophenotypes) which are now readily measurable at a large scale across diverse individuals. The potential of using endophenotypes for dissecting traits of interest remains underexplored in plants. The work presented here illustrated the utility of a large-scale (299 genotype and 7 tissue) gene expression resource to dissect traits across multiple levels of biological organization. Using single-tissue- and multi-tissue-based transcriptome-wide association studies (TWAS), we revealed that about half of the functional variation for agronomic and seed quality (carotenoid, tocochromanol) traits is regulatory. Comparing the efficacy of TWAS with genome-wide association studies (GWAS) and an ensemble approach that combines both GWAS and TWAS, we demonstrated that results of TWAS in combination with GWAS increase the power to detect known genes and aid in prioritizing likely causal genes. Using a variance partitioning approach in the independent maize Nested Association Mapping (NAM) population, we also showed that the most strongly associated genes identified by combining GWAS and TWAS explain more heritable variance for a majority of traits, beating the heritability captured by the random genes and the genes identified by GWAS or TWAS alone. This improves not only the ability to link genes to phenotypes, but also highlights the phenotypic consequences of regulatory variation in plants.\n\nAuthor summaryWe examined the ability to associate variability in gene expression directly with terminal phenotypes of interest, as a supplement linking genotype to phenotype. We found that transcriptome-wide association studies (TWAS) are a useful accessory to genome-wide association studies (GWAS). In a combined test with GWAS results, TWAS improves the capacity to re-detect genes known to underlie quantitative trait loci for kernel and agronomic phenotypes. This improves not only the capacity to link genes to phenotypes, but also illustrates the widespread importance of regulation for phenotype.

genetics↗

Leveraging mutational burden for complex trait prediction in sorghum

Sorghum (Sorghum bicolor (L.) Moench) is a major staple food cereal for millions of people worldwide. The sorghum genome, like other species, accumulates deleterious mutations, likely impacting its fitness. Though selection keeps deleterious mutations rare, their complete removal from the genome is impeded due to lack of recombination, drift, and their coupling with favorable loci. To study how deleterious mutations impact agronomic phenotypes, we identified putative deleterious mutations among ~5.5M segregating variants of 229 diverse sorghum lines. We provide the whole-genome estimate of the deleterious burden in sorghum, showing that about 33% of nonsynonymous substitutions are putatively deleterious. The pattern of mutation burden varies appreciably among racial groups; the caudatum shows higher mutation burden while the guinea has lower burden. Across racial groups, the mutation burden correlated negatively with biomass, plant height, Specific Leaf Area (SLA), and tissue starch content, suggesting deleterious burden decreases trait fitness. Putatively deleterious variants explain roughly half of the genetic variance. However, there is only moderate improvement in total heritable variance explained for biomass (7.6%) and plant height (5.2%). There is no advantage in total heritable variance for SLA and starch. The contribution of putatively deleterious variants to phenotypic diversity therefore appears to be dependent on the genetic architecture of traits. Overall, our results suggest that including putatively deleterious variants in models do not significantly improve breeding accuracy because of extensive linkage. However, knowledge of deleterious variants could be leveraged for sorghum breeding through genome editing.

genetics↗