Biology subjects

Asp, T.

Publications and source records attributed to Asp, T..

11 recordsLinked to original sources

bioRxiv2026

Genomic prediction of single cross families of perennial ryegrass in two nitrogen managements

The performance of a single cross is determined by the average additive effects of the parents, as well as the interactions between them. These quantities can be estimated using an appropriate genetic design, allowing for the estimation of general (GCA) and specific (SCA) combining abilities. The prediction of GCA for new parents and the total genetic value of unrealized crosses can be made when genome-wide marker information is available. Several studies in crops such as maize and rice have demonstrated the potential of genomic-assisted prediction of single-cross performance in economically important crops. However, no study to date has explored its relevance in perennial ryegrass, an obligate allogamous species that is bred in genetically heterogeneous families. In this study, we aimed to estimate genetic parameters and assess the ability of genomic models to predict the performance of F2 families in terms of dry matter yield and nutritive quality traits. We used data from a large partial diallel involving 104 parents from two distinct subpopulations, as inferred by admixture analysis. F2 families were evaluated in multiple environments and under two nitrogen availability conditions. Genotyping-by-sequencing of the parent plants produced 42,145 variants after quality control, which were used to estimate genomic relationships based on identity-by-state. Variance component estimation revealed limited GCA and SCA interactions with the environment, and particularly with nitrogen management. The predictive abilities of two parental models exceeded 0.60 and often surpassed 0.70 for most traits. However, incorporating non-additive effects into the model did not improve predictive ability. We leveraged the genetic diversity among parents to map genomic regions associated with all recorded traits. Genome-wide association studies (GWAS) by genomic best linear unbiased prediction (GBLUP) identified six quantitative trait loci (QTL) regions, with 45 candidate genes within the linkage disequilibrium range, estimated at approximately 92 kb. Our results demonstrate that genomic prediction of single crosses can be performed with high accuracy, especially when both parents are also progenitors of families in the training set.

genomics↗

bioRxiv2026

In vivo validation of predicted fitness effects at single-base resolution in a Brachypodium distachyon mutant population

Computational tools, including biological language models (LMs), show substantial promise in predicting the impact of genetic variants on plant fitness. However, validating variant effect predictions (VEP) requires experimental populations where genetic variation consists of discrete point mutations rather than segregating recombination blocks. In this study, we generated a novel population of Brachypodium distachyon mutant lines to evaluate the accuracy of VEP at single-base resolution. These lines were advanced through single-seed descent for five generations (M1 to M5), with whole-genome sequencing performed at M2 and M5 and phenotypic measurements recorded at M3 and M4. Using state-of-the-art VEP models, we predicted the functional impact of missense protein-coding variants and gene-proximal non-coding variants. We validated these predictions by estimating the effect of mutations on whole-plant measurements (burden tests) and their probability of fixation from M2 to M5 (purging tests). Among missense variants, the protein LM ESM showed superior predictive accuracy compared to the bioinformatic standard SIFT and the genomic LM PlantCAD. Notably, the relationship between VEP scores and allele fixation suggested a log-linear relationship between VEP scores and variant fitness. Among gene-proximal variants, PlantCAD appeared more accurate than supervised models of regulatory activity, such as chromatin accessibility (a2z) and RNA abundance (PhytoExpr). Collectively, our findings highlight the utility of state-of-the-art VEP tools as predictors of fitness and demonstrate the potential of mutant populations to evaluate computational tools for precision breeding applications.

genomics↗

bioRxiv2026

Genomic language models improve cross-species gene expression prediction and accurately capture regulatory variant effects in Brachypodium mutant lines

Predicting gene expression from cis-regulatory DNA sequences at the promoter and terminator regions is a central challenge in plant genomics. This capability is also a prerequisite for assessing the effects of regulatory mutations on gene expression. Here, we developed deep learning sequence-to-expression (S2E) models that leverage context-aware sequence embeddings from the PlantCaduceus genomic language model instead of one-hot encoding of sequences, to predict gene expression across 17 plant species. To further improve predictions, we integrated chromatin accessibility data as auxiliary regulatory features. First, we evaluated our models to predict gene expression on unseen gene families via cross-validation, demonstrating our models prediction accuracy across all species outperforms PhytoExpr, the current state-of-the-art (SOTA) S2E model in plants (Pearson R=0.82 vs. R=0.74). We then validated variant effect predictions using an experimental dataset across 796 Brachypodium mutant lines, specifically designed to test predictions at single-base resolution. Our models outperformed SOTA S2E models in predicting between-gene expression differences (regression coefficient {beta}=0.78 vs. {beta}=0.57). Remarkably, they also accurately predicted the effects of single-nucleotide mutations on within-gene expression, while SOTA S2E models showed only weak associations (regression coefficient {beta}=0.38 vs. {beta}=0.08). Our results demonstrated the value of context-aware DNA sequence embeddings for predicting regulatory variant effects in plants. They also reveal a persistent accuracy gap in S2E models when moving from between-gene to allelic variation, a challenge that needs to be addressed in future S2E studies.

bioinformatics↗

bioRxiv2025

Semi-automated image analysis of root architecture and early root development in faba bean and white clover and genomic estimation of breeding values and correlations

Protein-rich leguminous plants, such as faba bean and white clover are prospectively interesting crops in the North-European countries for reducing dependence on soybean import. Significant expansion of the production area of leguminous crops is challenged by the sub-optimal climatic conditions in this region, especially by the increasing probability of year-to-year fluctuation of extreme weather conditions due to global climate change. To overcome these challenges, development of new climate-resilient varieties suitable for growing under Northern-European conditions are needed. Root architecture and early root development, as well as the availability of efficient root phenotyping technologies are crucial factors of advancing in breeding of adequate varieties. We report a study of a simple and affordable screening technology of early root development using rhizoboxes in connection with semi-automated image analysis and provide a conceptual pipeline for estimation of Genomic Estimated Breeding Values (GEBVs) and correlating greenhouse and field phenotype data. Based on bivariate models, high genetic correlation (r=0.83) could be detected between total root length values recorded in greenhouse rhizobox experiments and field grain yield in faba bean. In white clover, moderately positive genetic correlation (r=0.17) between estimated breeding values of rhizobox-detected total root length and field yield could be identified. Our results suggest that phenotyping and selection of early root development components could potentially be useful in breeding programs to increase the genetic gain for field yield.

plant biology↗

bioRxiv2025

Genomic prediction of agronomic traits in perennial ryegrass (Lolium perenne L.) and genotype x environment interactions at the limit of the species distribution

BackgroundIn breeding the aim is to identify and accumulate beneficial variants. However, detection of these variants may be challenging in the presence of extensive genotype x environment interactions (GxE), as variant effects will be conditional on environment. MethodsThe study assesses the performance of 264 diploid perennial ryegrass accessions in a multi-environment field trial. We investigate the extent of GxE, for yield (total dry matter) and persistence traits, i.e. winter kill and spring cover, under environmental conditions experienced in Nordic and Baltic regions at the limit of the species distribution. Two different approaches to modelling GxE were tested: reaction norm and envirotyping, and the models were validated under three different breeding scenarios. ResultsOur analysis documented the presence of significant GxE interaction for all traits investigated in the study. Validation showed improvements in prediction accuracy when accounting for GxE: up to 4% for yield when predicting in unobserved environments, and up to 22% and 9% for spring cover and winter kill, respectively when predicting unobserved germplasm. Genome-wide-association-studies (GWAS) were utilized to detect genetic variants with marginal effects (environment-independent effect) and conditional effects (environment-dependent effects). Results showed the presence of large-effect genetic variants with marginal effects, in addition to few QTL whose effects were adaptive under specific environmental conditions while neutral or deleterious under different environmental conditions. ConclusionThis study demonstrates the usefulness and limitations of genomic prediction models for predicting GxE in highly diverse samples, and describes the extent of GxE interactions at the limit of species distribution for perennial ryegrass. Finally, our study points toward adaptive variation, which may enhance persistence of perennial ryegrass populations in Nordic and Baltic growing conditions.

genetics↗

bioRxiv2024

Automated Seminal Root Angle Measurement with Corrective Annotation

Measuring seminal root angle is an important aspect of root phenotyping, yet automated methods are lacking. We introduce SeminalRootAngle, a novel open-source automated method that measures seminal root angles from images. To ensure our method is flexible and user-friendly we build on an established corrective annotation training method for image segmentation. We tested SeminalRootAngle on a heterogeneous dataset of 662 spring barley rhizobox images, which presented challenges in terms of image clarity and root obstruction. Validation of our new automated pipeline against manual measurements yielded a Pearson correlation coefficient of 0.71. We also measure inter-annotator agreement, obtaining a Pearson correlation coefficient of 0.68, indicating that our new pipeline provides similar root angle measurement accuracy to manual approaches. We use our new SeminalRootAngle tool to identify SNPs significantly associated with angle and length, shedding light on the genetic basis of root architecture.

plant biology↗

bioRxiv2022

Genetic architecture of inter-specific and -generic grass hybrids by network analysis on multi-omics data

Understanding the mechanisms underlining forage production and its biomass nutritive quality at the omics level is crucial for boosting the output of high-quality dry matter per unit of land. Despite the advent of multiple omics integration for the study of biological systems in major crops, investigations on forage species are still scarce. Therefore, this study aimed to combine multi-omics from grass hybrids by prioritizing omic features based on the reconstruction of interacting networks and assessing their relevance in explaining economically important phenotypes. Transcriptomic and NMR-based metabolomic data were used for sparse estimation via the fused graphical lasso, followed by modularity-based gene expression and metabolite-metabolite network reconstruction, node hub identification, omic-phenotype association via pairwise fitting of a multivariate genomic model, and machine learning-based prediction study. Analyses were jointly performed across two data sets composed of family pools of hybrid ryegrass (Lolium perenne x L. multiflorum) and Festulolium loliaceum (L. perenne x Festuca pratensis), whose phenotypes were recorded for eight traits in field trials across two European countries in 2020/21. Our results suggest substantial changes in gene co-expression and metabolite-metabolite network topologies as a result of genetic perturbation by hybridizing L. perenne with another species within the genus relative to across genera. However, conserved hub genes and hub metabolomic features were detected between pedigree classes, some of which were highly heritable and displayed one or more significant edges with agronomic traits in a weighted omics-phenotype network. In spite of tagging relevant biological molecules as, for example, the light-induced rice 1 (LIR1), hub features were not necessarily better explanatory variables for omics-assisted prediction than features stochastically sampled. The use of the graphical lasso method for network reconstruction and identification of biological targets is discussed with an emphasis on forage grass breeding.

genetics↗

bioRxiv2022

Fine-mapping and comparative genomic analysis reveal the gene composition at the S and Z self-incompatibility loci in grasses

Self-incompatibility (SI) is a genetic mechanism of hermaphroditic plants to prevent inbreeding after self-pollination. Allogamous Poaceae species exhibit a unique gametophytic SI system controlled by two multi-allelic and independent loci, S and Z. Despite intense research efforts in the last decades, the genes that determine the initial recognition mechanism are yet to be identified. Here, we report the fine-mapping of the Z-locus in perennial ryegrass (Lolium perenne L.) and provide evidence that the pollen and stigma components are determined by two genes encoding DUF247 domain proteins (ZDUF247-I and ZDUF247-II) and the gene sZ, respectively. The pollen and stigma determinants are located side-by-side and were genetically linked in 10,245 individuals of two independent mapping populations segregating for Z. Moreover, they exhibited high allelic diversity as well as tissue-specific gene expression, matching expected characteristics of SI determinants known from other systems. Revisiting the S-locus using the latest high-quality whole-genome assemblies revealed a similar gene composition and structure as found for Z, supporting the hypothesis of a duplicated origin of the two-locus SI system of grasses. Ultimately, comparative genomic analyses across a wide range of self-compatible and self-incompatible Poaceae species revealed that the absence of a functional copy of at least one of the six putative SI determinants is accompanied by a self-compatible phenotype. Our study provides new insights into the origin and evolution of the unique gametophytic SI system in one of the largest and economically most important plant families.

plant biology↗

bioRxiv2022

Leveraging spatio-temporal genomic breeding value estimates of dry matter yield and herbage quality in ryegrass via random regression models

Joint modeling of correlated multi-environment and multi-harvest data of perennial crop species may offer advantages in prediction schemes and a better understanding of the underlying dynamics in space and time. The goal of the present study was to investigate the relevance of incorporating the longitudinal dimension of within-season multiple harvests of biomass yield and nutritive quality traits of forage perennial ryegrass (Lolium perenne L.) in a reaction norm model setup that additionally accounts for genotype-environment interactions. Genetic parameters and accuracy of genomic breeding value predictions were investigated by fitting three random regression (random coefficients) linear mixed models (gRRM) using Legendre polynomial functions to the data. All models accounted for heterogeneous residual variance and moving average-based spatial adjustments within environments. The plant material consisted of 381 bi-parental family pools and four check varieties of diploid perennial ryegrass evaluated in eight environments for biomass yield and nutritive quality traits. The longitudinal dimension of the data arose from multiple harvests performed four times annually. The specified design generated a total of 16,384 phenotypic data points for each trait. Genomic DNA sequencing was performed using DNA nanoball-based technology (DNBseq) and yielded 56,645 single nucleotide polymorphisms (SNPs) which were used to calculate the allele frequency-based genomic relationship matrix used in all genomic random regression models. Biomass yields estimated additive genetic variance and heritability values were higher in later harvests. The additive genetic correlations were moderate to low in early measurements and peaked at intermediates, with fairly stable values across the environmental gradient, except for the initial harvest data collection. This led to the conclusion that complex genotype-by-environment interaction (GxE) arises from spatial and temporal dimensions in the early season, with lower re-ranking trends thereafter. In general, modeling the temporal dimension with a second-order orthogonal polynomial in the reaction norm mixed model framework improved the accuracy of genomic estimated breeding value prediction for nutritive quality traits, but no gain in prediction accuracy was detected for dry matter yield. This study leverages the flexibility and usefulness of gRRM models for perennial ryegrass research and breeding and can be readily extended to other multi-harvest crops.

genetics↗

bioRxiv2020

A chromosome-scale Lotus japonicus Gifu genome assembly indicates that symbiotic islands are not general features of legume genomes

AimLotus japonicus is a herbaceous perennial legume that has been used extensively as a genetically tractable model system for deciphering the molecular genetics of symbiotic nitrogen fixation. Our aim is to improve the L. japonicus reference genome sequence, which has so far been based on Sanger and Illumina sequencing reads from the L. japonicus accession MG-20 and contained a large fraction of unanchored contigs. Methods and ResultsHere, we use long PacBio reads from L. japonicus Gifu combined with Hi-C data and new high-density genetic maps to generate a high-quality chromosome-scale reference genome assembly for L. japonicus. The assembly comprises 554 megabases of which 549 were assigned to six pseudomolecules that appear complete with telomeric repeats at their extremes and large centromeric regions with low gene density. Conclusion and PerspectivesThe new L. japonicus Gifu reference genome and associated expression data represent valuable resources for legume functional and comparative genomics. Here, we provide a first example by showing that the symbiotic islands recently described in Medicago truncatula do not appear to be conserved in L. japonicus.

genomics↗

bioRxiv2019

The mitogenome of Norway spruce and a reappraisal of mitochondrial recombination in plants

Plant mitogenomes can be difficult to assemble because they are structurally dynamic and prone to intergenomic DNA transfers, leading to the unusual situation where an organelle genome is far outnumbered by its nuclear counterparts. As a result, comparative mitogenome studies are in their infancy and some key aspects of genome evolution are still known mainly from pre-genome, qualitative methods. To help address these limitations, we combined machine learning and in silico enrichment of mitochondrial-like long reads to assemble the bacterial-sized mitogenome of Norway spruce (Pinaceae: Picea abies). We conducted comparative analyses of repeat abundance, intergenomic transfers, substitution and rearrangement rates, and estimated repeat-by-repeat homologous recombination rates. Prompted by our discovery of highly recombinogenic small repeats in P. abies, we assessed the genomic support for the prevailing hypothesis that intramolecular recombination is predominantly driven by repeat length, with larger repeats facilitating DNA exchange more readily. Overall, we found mixed support for this view: recombination dynamics were heterogeneous across vascular plants and highly active small repeats (ca. 200 bp) were present in about a third of studied mitogenomes. As in previous studies, we did not observe any robust relationships among commonly-studied genome attributes, but we identify variation in recombination rates as a underinvestigated source of plant mitogenome diversity.

genomics↗