P293
Fine Mapping the Un8 Locus Controlling Resistance to True Loose Smut in Barley

Date: Monday, January 13, 2014
Room: Grand Exhibit Hall
Wen Zang , Department of Plant Sciences, University of Saskatchewan, Saskatoon, SK, Canada
Peter E. Eckstein , Department of Plant Sciences, University of Saskatchewan, Saskatoon, SK, Canada
Graham J. Scoles , Department of Plant Sciences, University of Saskatchewan, Saskatoon, SK, Canada
Aaron D. Beattie , Crop Development Centre, University of Saskatchewan, Saskatoon, SK, Canada
True loose smut of barley, caused by the basidiomycete pathogen Ustilago nuda (Jens.) Rostr. (U. nuda), is a common disease in Western Canada and the United States. Traditional breeding for resistance to true loose smut is both labor-intensive and time-consuming. Molecular marker-assisted selection (MMAS) for true loose smut resistance is one of the best examples of how markers can improve the efficiency of selection since significant increases in efficiency and accuracy are achievable. Among the true loose smut resistance genes, Un8 is the most effective and long-lived resistance. Here we report progress made in fine mapping the Un8 interval which is essential for positional cloning of the gene. A variety of strategies including synteny, gene expression data, BAC and whole-genome sequence information, were used to saturate the Un8 region. A population of 4,700 F4 lines segregating for Un8 was used to delimit the Un8 gene to a 0.13 cM interval on chromosome 1HL, and assign it to FPC contig_546. Two sequences located close to a marker co-segregating with Un8 showed high BLAST hit scores to disease resistance genes. One sequence matched a serine/threonine protein kinase and the other matched a NBS-LRR type resistance gene. Sequencing and expression analysis of these two sequences is currently underway to determine their potential to be the Un8 gene.