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The Coiled-Coil NLR Rph1, Confers Leaf Rust Resistance in Barley Cultivar Sudan
PM. Dracatos, J. Bartoš, H. Elmansour, D. Singh, M. Karafiátová, P. Zhang, B. Steuernagel, R. Svačina, JCA. Cobbin, B. Clark, S. Hoxha, MS. Khatkar, J. Doležel, BB. Wulff, RF. Park,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
BB/P016855/1
Biotechnology and Biological Sciences Research Council - United Kingdom
NLK
Free Medical Journals
od 1926 do Před 1 rokem
Open Access Digital Library
od 1926-01-01
PubMed
30593453
DOI
10.1104/pp.18.01052
Knihovny.cz E-zdroje
- MeSH
- interakce hostitele a patogenu * MeSH
- ječmen (rod) fyziologie MeSH
- mapování chromozomů MeSH
- NLR proteiny fyziologie MeSH
- rostlinné geny MeSH
- rostlinné proteiny fyziologie MeSH
- sekvenční analýza DNA MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Unraveling and exploiting mechanisms of disease resistance in cereal crops is currently limited by their large repeat-rich genomes and the lack of genetic recombination or cultivar (cv)-specific sequence information. We cloned the first leaf rust resistance gene Rph1 (Rph1a) from cultivated barley (Hordeum vulgare) using "MutChromSeq," a recently developed molecular genomics tool for the rapid cloning of genes in plants. Marker-trait association in the CI 9214/Stirling doubled haploid population mapped Rph1 to the short arm of chromosome 2H in a physical region of 1.3 megabases relative to the barley cv Morex reference assembly. A sodium azide mutant population in cv Sudan was generated and 10 mutants were confirmed by progeny-testing. Flow-sorted 2H chromosomes from Sudan (wild type) and six of the mutants were sequenced and compared to identify candidate genes for the Rph1 locus. MutChromSeq identified a single gene candidate encoding a coiled-coil nucleotide binding site Leucine-rich repeat (NLR) receptor protein that was altered in three different mutants. Further Sanger sequencing confirmed all three mutations and identified an additional two independent mutations within the same candidate gene. Phylogenetic analysis determined that Rph1 clustered separately from all previously cloned NLRs from the Triticeae and displayed highest sequence similarity (89%) with a homolog of the Arabidopsis (Arabidopsis thaliana) disease resistance protein 1 protein in Triticum urartu In this study we determined the molecular basis for Rph1-mediated resistance in cultivated barley enabling varietal improvement through diagnostic marker design, gene editing, and gene stacking technologies.
Faculty of Veterinary Science The University of Sydney Camden NSW 2570 Australia
John Innes Centre Norwich NR4 7UH United Kingdom
School of Life and Environmental Sciences The University of Sydney Sydney NSW 2006 Australia
Citace poskytuje Crossref.org
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