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Vandenberg, A.

Publications and source records attributed to Vandenberg, A..

13 recordsLinked to original sources

Variability in mineral composition of Canadian lentil cultivars

Lentils are a good source of essential minerals for the proper functioning of the human body. We evaluated 34 cultivars and elite lentil lines representing the breadth of the Canadian breeding program. Trials were established in 10 site-years across Saskatchewan Province. Concentrations of 27 minerals were quantified with an inductive coupled argon plasma emission spectrometer in whole and dehulled lentil seeds. Li, V, Cr, Co, As, Ag, Cd, Sn, La, Hg, and Pb had concentrations below the quantification limit and were excluded from further analysis. The effects of site year, tissue type (whole and dehulled), and lentil genotypes were analyzed using a mixed model. Mineral concentrations of Na, K, Ca, Mg, Cu, B, and Ba were stable across site years. Na, Zn, P, Cu, Se, and Mo had similar concentrations in whole and dehulled seeds. Ca, Fe, Mg, Mn, B, Al, and Ba were more concentrated in whole seeds, while K, S, and Ni were higher in dehulled seeds. Several lentil genotypes had outstanding concentrations of several minerals. Lentil genotypes with a higher composition of several minerals could be a starting point for enhancing mineral composition in lentils.

genetics↗

Understanding Genome Structure Facilitates the Use of Wild Lentil Germplasm for Breeding: A Case Study with Shattering Loci

Plant breeders are generally reluctant to cross elite crop cultivars with their wild relatives to introgress novel desirable traits due to associated negative traits such as pod shattering. This results in a genetic bottleneck that could be reduced through better understanding of the genomic locations of the gene(s) controlling this trait. We integrated information on parental genomes, pod shattering data from multiple environments, and high-density genetic linkage maps to identify pod shattering QTLs in three lentil interspecific recombinant inbred line (RIL) populations. The broad-sense heritability on a multi-environment basis varied from 0.46 (in LR-70, Lens culinaris x L. odemensis) to 0.77 (in LR-68, L. orientalis x L. culinaris). Genetic linkage maps of the interspecific populations revealed reciprocal translocations of chromosomal segments that differed among the populations, and which were associated with reduced recombination. Segregation distortion was also observed for clusters of SNPs on multiple chromosomes per population, further affecting introgression. Two major QTL, on chromosomes 4 and 7, were repeatedly detected in the three populations and contain several candidate genes. These findings will be of significant value for lentil breeders to strategically access novel superior alleles while minimizing the genetic impact of pod shattering from wild parents.

plant biology↗

QTL Mapping of Seed Fe Concentration in an Interspecific RIL Population Derived from Lens culinaris x Lens ervoides

Biofortification of lentil (Lens culinaris Medik.) was investigated to potentially increase bioavailable iron (Fe) in the human diet. This study assessed the genetic variation for seed Fe concentration (SFeC) and identified the genomic regions associated with SFeC in an interspecific mapping population derived from crossing between L. culinaris cv. Eston and L. ervoides accession IG 72815. A total of 134 RILs were evaluated in three environments. The SFeC data for individual environments and best linear unbiased prediction (BLUP) of the SFeC across environments were used for QTL analysis. The seeds of the RILs exhibited variation for SFeC from 47.0 to 102.9 mg kg-1 and several RILs showed transgressive segregation for SFeC. QTL analysis identified two QTLs on chromosomes 2 and 6 that accounted for 11.9-14.0% and 12.5-20.5%, respectively, of the total phenotypic variation for SFeC. The SNP markers linked to the identified QTLs may prove useful for increasing SFeC via marker-assisted selection. RILs with high SFeC can be incorporated into the lentil breeding program to broaden the genetic base of the breeding pool and/or used for the development of genetic resources for future genomic studies.

genomics↗

Dissection of genotype-by-environment interaction and simultaneous selection for grain yield and stability in faba bean (Vicia faba L.)

Increasing faba bean production is indispensable to supply the growing demand for plant-based protein on the global scale. A thorough understanding of genotype (G) x environment (E) interaction (GEI) patterns is critical to developing high-yielding varieties with wider adaptation. Thirteen faba bean genotypes were evaluated in 15 environments during 2019-2020 in western Canada to estimate their yield stability using different stability statistics. The combined analysis of variance and additive main effects and multiplicative interaction (AMMI) analysis revealed that G, E, and GEI effects were highly significant (P<0.001), indicating differential responses of the genotypes across the environments, enabling the stability analysis. The result of the model comparison found the best linear unbiased prediction (BLUP) to outperform AMMI models. The BLUP-based biplot of the weighted average of absolute scores (WAASB) stability and mean grain yield identified AO1155 (Navi), 1089-1-2, 1310-5, DL Tesoro, and 1239-1 as high-yielding and stable genotypes. The correlation analysis revealed that most of the stability parameters had a strong association with grain yield and with each other, indicating that they should be used in combination with one another to select genotypes with high yield. Overall, the WAASB superiority index (WAASBY) and the average sum of ranks of all stability statistics identified the same genotypes in terms of high yielding and stability, and genotype AO1155 is considered the most stable and highest yielding among the tested genotypes. Genotypes with stable yields across environments would be beneficial for faba bean genetic improvement programs globally. Core IdeasO_LIStability analysis was estimated using 13 faba bean genotypes over 15 site-years. C_LIO_LIThe different stability methods described genotypic performance in different ways. C_LIO_LIThe majority of stability models showed a strong rank correlation with grain yield. C_LIO_LIAMMI and BLUP analyses revealed a highly significant GxE interaction, with BLUP outperforming AMMI. C_LIO_LIOverall, the employed stability statistics identified AO1155 as the highest yielding and most stable genotype. C_LI

plant biology↗

Genomic regions associated with chocolate spot (Botrytis fabae Sard.) resistance in fababean (Vicia faba L.)

Chocolate spot (CS), caused by Botrytis fabae Sard., is an important threat to global faba bean production. Growing resistant faba bean cultivars is, therefore, paramount to preventing yield loss. To date, there have been no reported quantitative trait loci (QTLs) associated with CS resistance in faba bean. The objective of this study was to identify genomic regions associated with CS resistance using a recombinant inbred line (RIL) population derived from resistant accession ILB 938. A total of 165 RILs from the cross Melodie/2 x ILB 938/2 were genotyped and evaluated for CS reactions under replicated controlled climate conditions. QTL analysis identified five loci contributing to CS resistance on faba bean chromosomes 1 and 6, accounting for 5.0-23.4% of the total phenotypic variance. The sequences of SNP markers linked to resistance QTLs on chromosome 1 that have the largest effects encode multiple classes of putative disease and/or defense-related genes. The results of this study not only provide insight into disease-resistance QTLs, but also can be used as potential targets for marker-assisted breeding in faba bean genetic improvement for CS resistance. Key messageQTL mapping identified key genomic regions associated with chocolate spot resistance on faba bean chromosomes 1 and 6, which may serve as novel genetic tools to develop disease-resistant faba bean cultivars.

genomics↗

Genomic rearrangements have consequences for introgression breeding as revealed by genome assemblies of wild and cultivated lentil species

Understanding the genomic relationship between wild and cultivated genomes would facilitate access to the untapped variability found in crop wild relatives. We developed genome assemblies of a cultivated lentil (Lens culinaris) as well as a wild relative (L. ervoides). Comparative analyses revealed large-scale structural rearrangements and additional repetitive DNA in the cultivated genome, resulting in regions of reduced recombination, segregation distortion and permanent heterozygosity in the offspring of a cross between the two species. These novel findings provide plant breeders with better insight into how best to approach accessing the novel variability available in wild relatives.

plant biology↗

Identification of anthracnose (Colletotrichum lentis) race 1 resistance loci in lentil by integrating linkage mapping and a genome-wide association study

Anthracnose, caused by Colletotrichum lentis, is a devastating disease of lentil in Western Canada. Growing resistant lentil cultivars is the most cost-effective and environmentally friendly approach to prevent seed yield losses that can exceed 70%. To identify loci conferring resistance to anthracnose race 1 in lentil, biparental quantitative trait loci (QTL) mapping of two recombinant inbred line (RIL) populations was integrated with a genome-wide association study (GWAS) using 200 diverse lentil accessions from a lentil diversity panel (LDP). A major-effect QTL (qAnt1.Lc-3) conferring resistance to race 1 was mapped to lentil chromosome 3 and co-located on the lentil physical map for both RIL populations. Clusters of candidate nucleotide binding-leucine-rich repeats (NB-LRR) and other defense-related genes were uncovered within the QTL region. A GWAS detected 14 significant SNP markers associated with race 1 resistance on chromosomes 3, 4, 5, and 6. The most significant GWAS SNPs on chromosome 3 supported qAnt1.Lc-3 and delineated a region of 1.6 Mb containing candidate resistance genes. The identified SNP markers can be directly applied in marker-assisted selection to accelerate the introgression of race 1 resistance in lentil breeding.

genomics↗

Genetic and gene expression analysis of flowering time regulation by light quality in lentil

Flowering time is important due to its roles in adaptation to different environments and subsequent formation of crop yield. Changes in light quality affect a range of developmental processes including flowering time, however little is known about light quality induced flowering time control in lentil. This study aims to investigate the genetic basis for differences in flowering response to light quality in lentil. We explored variation in flowering time caused by changes in red/far-red related light quality environments of a lentil interspecific recombinant inbred line population developed from a cross between Lens culinaris cv. Lupa and L. orientalis accession BGE 016880. A genetic linkage map was constructed and then used for identifying QTL associated with flowering time regulation under different light quality environments. Differential gene expression analysis through transcriptomic study and RT-qPCR were used to identify potential candidate genes. QTL mapping located 13 QTLs controlling flower time under different light quality environments, with phenotypic variance explained ranging from 1.7 to 62.9%. Transcriptomic profiling and gene expression analysis for both parents of this interspecific RIL population identified flowering-related genes showing environment-specific differential expression (flowering DEGs). One of these, a member of the florigen gene family FTa1 (LcFTa1) was located close to 3 major QTLs. Furthermore, gene expression results suggests two other florigen genes (LcFTb1 and LcFTb2), MADS-box transcription factors like LcAGL6/13d, LcSVPb, LcSOC1b and LcFULb, as well as bHLH transcription factor LcPIF6 and Gibberellin 20 oxidase LcGA20oxC,G, may be involved in the light quality response as well. Our results show that a major component of flowering time sensitivity to light quality is tightly linked to LcFTa1 and associated with changes in its expression. This work provides a foundation for crop improvement of lentil with better adaptation to variable light environments.

plant biology↗

An advanced lentil backcross population developed from a cross between Lens culinaris x L. ervoides for future disease resistance and genomic studies

Genetically accessible variation to some of the abiotic and biotic stresses are limited in the cultivated lentil (Lens culinaris Medik.) germplasm. Introgression of novel alleles from its wild relative species might be required for enhancing the genetic improvement of the crop. L. ervoides, one of the wild relatives of lentil, is a proven source of disease resistance for the crop. Here we introduce a lentil advanced backcross population (LABC-01) developed in cultivar CDC Redberry background, based on L. ervoides alleles derived from an interspecific recombinant inbred population, LR-59-81. Two-hundred and seventeen individuals of the LABC-01 population at BC2F3:4 generation were screened for the race 0 of anthracnose (Colletotrichum lentis) and stemphylium blight (Stemphylium botryosum) under controlled conditions. The population showed significant variations for both diseases and transfer of resistance alleles into the elite cultivar was evident. It also segregated for other traits such as days to flowering, seed coat colour, seed coat pattern and flower colour. Overall, we showed that LABC-01 population can be used in breeding programs worldwide to improve disease resistance and will be available as a valuable genetic resource for future genetic analysis of desired loci introgressed from L. ervoides.

plant biology↗

Validated B vitamin quantification from lentils by ultra-performance liquid chromatography selected reaction monitoring mass spectrometry

A validated method for B vitamin separation and quantification from lentil seeds using ultra-performance liquid chromatography-selected reaction monitoring mass spectrometry (UPLC-SRM MS) was reported. The use of three enzymes (acid phosphatase, {beta}-glucosidase, and rat serum) with a 4 h incubation was sufficient to convert bound B vitamins into their free forms. Twenty B vitamers were selected and a 5-min UPLC-SRM MS method was optimized for rapid analysis. This method was applied to quantify B vitamin concentration during lentil seed germination over a 5-day period. Total B vitamins increased up to 1.5-fold on day 5 (from 39.2 {micro}g/g to 60.6 {micro}g/g of dry weight) comparing with dry seeds. Vitamin B5 (pantothenic acid) was the most abundant B vitamin in both dry seeds (34.2%) and in germinated seeds (17.7%-24.5% of total B vitamins); B8 (biotin) and B12 (cyanocobalamin) were not detected in lentil samples.

biochemistry↗

Understanding photothermal interactions will help expand production range and increase genetic diversity of lentil (Lens culinaris Medik.)

O_LILentil (Lens culinaris Medik.) is cultivated under a wide range of environmental conditions, which led to diverse phenological adaptations and resulted in a decrease in genetic variability within breeding programs due to reluctance in using genotypes from other environments. C_LIO_LIWe phenotyped 324 genotypes across nine locations over three years to assess their phenological response to the environment of major lentil production regions and to predict days from sowing to flowering (DTF) using a photothermal model. C_LIO_LIDTF was highly influenced by the environment and is sufficient to explain adaptation. We were able to predict DTF reliably in most environments using a simple photothermal model, however, in certain site-years, results suggest there may be additional environmental factors at play. Hierarchical clustering of principal components revealed the presence of eight groups based on the responses of DTF to contrasting environments. These groups are associated with the coefficients of the photothermal model and revealed differences in temperature and photoperiod sensitivity. C_LIO_LIExpanding genetic diversity is critical to the success of a breeding program; understanding adaptation will facilitate the use of exotic germplasm. Future climate change scenarios will result in increase temperature and/or shifts in production areas, we can use the photothermal model to identify genotypes most likely to succeed in these new environments. C_LI

plant biology↗

VC1 catalyzes a key step in the biosynthesis of vicine from GTP in faba bean

Faba bean is a widely adapted and high-yielding legume cultivated for its protein-rich seeds1. However, the seeds accumulate the anti-nutritional pyrimidine glucosides vicine and convicine, which can cause haemolytic anaemia--favism--in the 400 million individuals genetically predisposed by a deficiency in glucose-6-phosphate dehydrogenase2. Here, we identify the first enzyme associated with vicine and convicine biosynthesis, which we name VC1. We show that VC1 co-locates with the major QTL for vicine and convicine content and that the expression of VC1 correlates highly with vicine content across tissues. We also show that low-vicine varieties express a version of VC1 carrying a small, frame-shift insertion, and that overexpression of wild-type VC1 leads to an increase in vicine levels. VC1 encodes a functional GTP cyclohydrolase II, an enzyme normally involved in riboflavin biosynthesis from the purine GTP. Through feeding studies, we demonstrate that GTP is a precursor of vicine both in faba bean and in the distantly related plant bitter gourd. Our results reveal an unexpected biosynthetic origin for vicine and convicine and pave the way for the development of faba bean cultivars that are free from these anti-nutrients, providing a safe and sustainable source of dietary protein.

biochemistry↗

Genomic selection for lentil breeding: empirical evidence

Genomic selection (GS) is a type of marker-based selection which was initially suggested for livestock breeding and is being encouraged for crop breeding. Several statistical models and approaches have been developed to implement GS; however, none of these methods have been tested for use in lentil breeding. This study was conducted to evaluate different GS models and prediction scenarios based on empirical data and to make recommendations for designing genomic selection strategies for lentil breeding. We evaluated nine single-trait models, two multiple-trait models, and models that account for population structure and genotype-by-environment interaction (GEI) using a lentil diversity panel and two recombinant inbred lines (RIL) populations that were genotyped using a custom exome capture assay. Within-population, across-population and across-environment predictions were made for five phenology traits. Prediction accuracy varied among the evaluated models, populations, prediction scenarios, traits, and statistical models. Single-trait models showed similar accuracy for each trait in the absence of large effect QTL but BayesB outperformed all models when there were QTL with relatively large effects. Models that accounted for GEI and multiple-trait (MT) models increased prediction accuracy for a low heritability trait by up to 66% and 14% but accuracy did not improve for traits of high heritability. Moderate to high accuracies were obtained for within-population and across-environment predictions but across-population prediction accuracy was very low. This suggests that GS can be implemented in lentil to make predictions within populations and across environments, but across-population prediction should not be considered when the population size is small.

genomics↗