Fine mapping and chromosome walking towards the Ror1 locus in barley (Hordeum vulgare L.) |
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Authors: | Johanna Acevedo-Garcia Nicholas C. Collins Nahal Ahmadinejad Lu Ma Andreas Houben Pawel Bednarek Mariam Benjdia Andreas Freialdenhoven Janine Altmüller Peter Nürnberg Richard Reinhardt Paul Schulze-Lefert Ralph Panstruga |
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Affiliation: | 1. Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany 3. Unit of Plant Molecular Cell Biology, Institute for Biology I, RWTH Aachen University, Worringer Weg 1, 52056, Aachen, Germany 2. Sainsbury Laboratory, John Innes Centre, Norwich Research Park, Norwich, NR4-7UH, UK 7. Australian Centre for Plant Functional Genomics, School of Agriculture Food and Wine, University of Adelaide, Glen Osmond, SA, 5064, Australia 8. INRES, Crop Bioinformatics, University of Bonn, Katzenburgweg 2, 53115, Bonn, Germany 4. Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), OT Gatersleben, Corrensstrasse 3, 06466, Stadt Seeland, Germany 10. Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704, Poznan, Poland 9. European Commission ERC Executive Agency, COV2, 1049, Brussels, Belgium 6. Institute for Biology I, RWTH Aachen University, Worringer Weg 1, 52056, Aachen, Germany 5. Cologne Center for Genomics (CCG), University of Cologne, Weyertal 115b, 50931, Cologne, Germany
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Abstract: | Key message The Ror1 gene was fine-mapped to the pericentric region of barley chromosome 1HL. Abstract Recessively inherited loss-of-function alleles of the barley (Hordeum vulgare) Mildew resistance locus o (Mlo) gene confer durable broad-spectrum disease resistance against the obligate biotrophic fungal powdery mildew pathogen Blumeria graminis f.sp. hordei. Previous genetic analyses revealed two barley genes, Ror1 and Ror2, that are Required for mlo-specified resistance and basal defence. While Ror2 was cloned and shown to encode a t-SNARE protein (syntaxin), the molecular nature or Ror1 remained elusive. Ror1 was previously mapped to the centromeric region of the long arm of barley chromosome 1H. Here, we narrowed the barley Ror1 interval to 0.18 cM and initiated a chromosome walk using barley yeast artificial chromosome (YAC) clones, next-generation DNA sequencing and fluorescence in situ hybridization. Two non-overlapping YAC contigs containing Ror1 flanking genes were identified. Despite a high degree of synteny observed between barley and the sequenced genomes of the grasses rice (Oryza sativa), Brachypodium distachyon and Sorghum bicolor across the wider chromosomal area, the genes in the YAC contigs showed extensive interspecific rearrangements in orientation and order. Consequently, the position of a Ror1 homolog in these species could not be precisely predicted, nor was a barley gene co-segregating with Ror1 identified. These factors have prevented the molecular identification of the Ror1 gene for the time being. |
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