Publications by authors named "Wubishet Bekele"

Pangenomes are collections of annotated genome sequences of multiple individuals of a species. The structural variants uncovered by these datasets are a major asset to genetic analysis in crop plants. Here we report a pangenome of barley comprising long-read sequence assemblies of 76 wild and domesticated genomes and short-read sequence data of 1,315 genotypes.

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SQUAMOSA promoter binding-like proteins (SPLs) are important transcription factors that influence growth phase transition and reproduction in plants. SPLs are targeted by miR156 but the SPL/miR156 module is completely unknown in oat. We identified 28 oat SPL genes (AsSPLs) distributed across all 21 oat chromosomes except for 4C and 6D.

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Three independent experiments with different genetic backgrounds mapped the resistance gene Pm7 in the oat genome to the distal part of the long arm of chromosome 5D. Resistance of oat to Blumeria graminis DC. f.

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Cultivated oat (Avena sativa L.) is an allohexaploid (AACCDD, 2n = 6x = 42) thought to have been domesticated more than 3,000 years ago while growing as a weed in wheat, emmer and barley fields in Anatolia. Oat has a low carbon footprint, substantial health benefits and the potential to replace animal-based food products.

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Article Synopsis
  • * The study uncovers significant links between candidate genes and quantitative trait loci (QTLs) related to important traits like heading date, oil levels, and β-glucan concentrations in the oats.
  • * Researchers also identify complex chromosome rearrangements, including a translocation and a possible inversion, which can complicate genetic mapping and the application of QTLs in oat breeding efforts.
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Cultivated oat (Avena sativa L.) is an important cereal grown worldwide due to its multifunctional uses for animal feed and human food. Oat has lagged behind other cereals in the genetic and genomic studies attributed to its large and complex genomes.

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Comparative sequence analysis was used to design a SNP marker that aided in the identification of new sources of oat stem rust resistance. New races of Puccinia graminis f. sp.

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Barley (Hordeum vulgare L.) is one of the most important global crops. The six-row barley cultivar Morex reference genome has been used by the barley research community worldwide.

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Identifying mechanisms and pathways involved in gene-environment interplay and phenotypic plasticity is a long-standing challenge. It is highly desirable to establish an integrated framework with an environmental dimension for complex trait dissection and prediction. A critical step is to identify an environmental index that is both biologically relevant and estimable for new environments.

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Article Synopsis
  • Genomic prediction in small breeding programs faces challenges due to high initial genotyping costs, which are often greater than field trial expenses.
  • Using a narrow-base biparental oat population, this study shows that utilizing a smaller number of markers for early and later generations can effectively implement genomic prediction.
  • By leveraging early generation genotyping, breeding programs can streamline the selection process, combining inexpensive dominant marker data with more costly codominant markers for better predictions across generations.
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Fusarium langsethiae is a symptomless pathogen of oat panicles that produces T-2 and HT-2 mycotoxins, two of the most potent trichothecenes produced by Fusarium fungi in cereals. In the last few years, the levels of these mycotoxin in oat grain has increased and the European commission have already recommended a maximum level for of 1000 μg kg for unprocessed oat for human consumption. The optimal and most sustainable way of combating infection and mycotoxin contamination is by releasing resistant oat varieties.

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Article Synopsis
  • Stem rust is a significant disease affecting cultivated oats, primarily controlled in North America through host resistance from a limited number of resistance genes.
  • Researchers focused on a specific resistance gene to develop high-density genetic maps and to create efficient DNA markers for selecting resistant oat varieties.
  • Their findings included identifying key markers linked to the resistance gene, which were successfully converted into KASP assays that can accurately predict the presence of the resistance gene in various oat lines and cultivars.
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Genotyping-by-sequencing (GBS)-derived molecular markers reveal the distinct genetic population structure and relatively narrow genetic diversity of Chinese hulless oat landraces. Four markers linked to the naked grain gene (N1) are identified by genome-wide association study (GWAS). Interest in hulless oat (Avena sativa ssp.

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Article Synopsis
  • Crown rust, a major disease affecting oats caused by the fungus f. sp. Eriks., leads to significant yield losses and is controlled in part by a gene-for-gene interaction that oat breeders utilize.
  • The study aimed to map a specific resistance gene in two independent oat populations and identify SNP markers to predict its presence in breeding material.
  • Results showed the resistance gene mapped to linkage group Mrg11 with specific SNP markers, allowing for the development of PCR assays to accurately predict resistance status and improve oat breeding programs through marker-assisted selection.
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Key message: Several AC Proteus derived genomic regions (QTLs, SNPs) have been identified which may prove useful for further development of high yielding high protein cultivars and allele-specific marker developments. High seed protein content is a trait which is typically difficult to introgress into soybean without an accompanying reduction in seed yield. In a previous study, 'AC Proteus' was used as a high protein source and was found to produce populations that did not exhibit the typical association between high protein and low yield.

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We adapted and tested a Rapture assay as an enhancement of genotyping-by-sequencing (GBS) in oat (Avena sativa). This assay was based on an additional bait-based capture of specific DNA fragments representing approximately 10,000 loci within the enzyme-based complexity reduction provided by GBS. By increasing the specificity of GBS to include only those fragments that provided effective polymorphic markers, it was possible to achieve deeper sequence coverage of target markers, while simultaneously sequencing a greater number of samples on a single unit of next-generation sequencing.

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Article Synopsis
  • The research focuses on developing detailed genome assemblies for two diploid progenitor species of the common oat, Avena atlantica and Avena eriantha, which can potentially improve the adaptive and food quality traits of cultivated oats.
  • The findings reveal that both genome assemblies are large, rich in repetitive sequences, and contain about 50,000 annotated genes, including key resistance gene analogs.
  • The study enhances understanding of common oat's evolution and genetics, including insights into subgenomic relationships and candidate genes linked to flowering time and disease resistance.
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Article Synopsis
  • * Pg13 is crucial for stem rust resistance in North American oat cultivars and will aid in routine selection practices like gene pyramiding and backcrosses.
  • * High-density linkage maps and genome-wide associations confirmed Pg13's location at approximately 67.7 cM on linkage group Mrg18, coinciding with specific translocation breakpoints and other resistance genes, with reliable KASP assays created for breeding use.
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The genus Avena (oats) contains diploid, tetraploid and hexaploid species that evolved through hybridization and polyploidization. Four genome types (named A through D) are generally recognized. We used GBS markers to construct linkage maps of A genome diploid (Avena strigosa x A.

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Article Synopsis
  • A study analyzed genetic variations in 4657 cultivated oat accessions using genotyping-by-sequencing, discovering over 164,000 tag-level genetic variants and significantly increasing marker density for mapping.
  • The research created chromosome-level haplotype maps that highlighted differences in haplotype size and diversity, informing potential for genomic analysis and selection in oats.
  • A combined genome-wide association study revealed 184 significant links to heading date, demonstrating that tag-level haplotypes offer superior mapping utility and promising prediction accuracies for genomic selection.
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Article Synopsis
  • 635 oat lines and 4561 SNP loci were analyzed to understand population structure, linkage disequilibrium (LD), and the relationship between genotypes and heading date.
  • The analysis revealed that 25.3% of genetic variation could be explained by the first five principal components, but no clear structured population was found, although clustering indicated differences between spring oats and southern U.S. origins.
  • Linkage disequilibrium was observed to decay slower in southern oat lines compared to spring oat lines, particularly highlighting an interesting case on linkage group Mrg28, and several linkage groups were consistently associated with heading date across different environments.
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Hexaploid oat ( L., 2 = 6 = 42) is a member of the Poaceae family and has a large genome (∼12.5 Gb) containing 21 chromosome pairs from three ancestral genomes.

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Article Synopsis
  • A genome analysis of 27 oat species revealed their evolutionary relationships and classified the genomes more accurately, particularly identifying the D genome in hexaploid oats.
  • The study employed genotyping-by-sequencing (GBS) methods that successfully aligned with earlier phylogenetic studies, confirming the reliability of GBS for understanding oat genetics.
  • The findings redefined the classification of certain tetraploid species and clarified the origins of chromosomes, emphasizing that no current diploids are closely related enough to be classified with the D genome.
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Genome size is an indicator of evolutionary distance and a metric for genome characterization. Here, we report accurate estimates of genome size in 99 accessions from 26 species of Avena. We demonstrate that the average genome size of C genome diploid species (2C = 10.

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