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Bedford, J. A.

Publications and source records attributed to Bedford, J. A..

2 recordsLinked to original sources

The barley ear row-number allele ancestral to the six-row allele vrs1.a1 is found in wild barley from the Fertile Crescent

Barley (Hordeum vulgare L.) exhibits two main inflorescence phenotypes: the wild-type two-row form in which only the central spikelet at each rachis node is fertile, and the six-row form, where mutations in the homeobox gene Six-rowed spike 1 (VRS1) confer fertility to all three spikelets. While the six-row alleles vrs1.a2 and vrs1.a3 arose independently from point mutations in the ancestral Vrs1.b2 and Vrs1.b3 alleles, the origin of the hypothesised wild-type Vrs1.b1 allele ancestral to vrs1.a1 is unclear. To explore the origin and exploitation of VRS1 alleles, we re-sequenced VRS1 in 98 cultivars, 170 landraces and 69 wild barley accessions, identifying 39 haplotypes. Sequence analysis confirmed vrs1.a1 as the most commonly used six-row allele in European cultivars. Subsequent analysis of the landrace and wild barley data identified three occurrences of the haplotype consistent with a vrs1.b1 allele, all from wild barley. These wild barley accessions originated from the eastern Fertile Crescent (Iran) and the Caspian Sea region, suggesting vrs1.a1 arose via mutation of Vrs1.b1 within barleys domestication centre - unlike vrs1.a2 and vrs1.a3, which originated in the Western Mediterranean and East Asia cultivated barley genepools, respectively. In addition, we identified ten novel VRS1 amino acid changes in wild barley accessions, which given the pleiotropic effects of VRS1 on traits such as leaf size, vein number and tiller number, may be of interest for future functional investigation. Overall, this study provides insights into the evolution, domestication and utilisation of genetic variation at VRS1, a key gene influencing barley architecture and agricultural performance.

molecular biology↗

Fraxinus excelsior updated long-read genome reveals the importance of MADS-box genes in tolerance mechanisms against ash dieback

Ash dieback caused by the fungus Hymenoscyphus fraxineus has devastated the European ash tree population since it arrived in Europe in 1992. Great effort has been put into breeding programmes to increase the genetic diversity of ash trees and find heritable genetic markers associated with resistance, or tolerance mechanisms, to ash dieback. To facilitate identification of molecular markers, we used Oxford Nanopore Technologies combined with Illumina sequencing to obtain an accurate and contiguous ash genome. We used this genome to reanalyse transcriptome data from a Danish ash panel of 182 tree accessions. Using associative transcriptomics, we identified 175 gene expression markers (GEMs), including 11 genes annotated as dormancy MADS-box transcription factors which are associated with ash bud dormancy, flowering and senescence. We hypothesize that tolerant trees both break dormancy earlier in the year by increasing the expression of flowering-related SOC1 MADS-box and reducing the expression of SVP-like MADS-box, whilst also accelerating senescence by increasing the expression of JOINTLESS MADS-box genes. DNA methylation differences in the promoters of MADS-box genes between one tolerant and one susceptible tree indicate potential epigenetic regulation of these traits. Article SummaryAsh dieback has devastated European ash tree populations. To aid in breeding programmes focused on finding solutions against this pathogen, we have assembled a new ash genome. This new genome helped us to identify genes related to tree biological life cycles, expressed differently in tolerant and susceptible trees. For the first time, we have also discovered that susceptible and tolerant trees showed different DNA methylation frequencies in those genes, suggesting epigenetic regulation. DNA methylation can turn on/off gene expression without changing the DNA sequence. These genes, and their regulatory elements, are ideal targets during breeding programmes combating this pathogen.

plant biology↗