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This article in CS

  1. Vol. 45 No. 6, p. 2563-2572
     
    Received: Mar 17, 2005


    * Corresponding author(s): muehl003@umn.edu
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doi:10.2135/cropsci2005.0236

Quantitative Trait Loci for Multiple Disease Resistance in Wild Barley

  1. S. J. Yuna,
  2. L. Gyenisd,
  3. P. M. Hayesb,
  4. I. Matusc,
  5. K. P. Smithd,
  6. B. J. Steffensone and
  7. G. J. Muehlbauer *d
  1. a Division of Biological Resources of Sciences, Chonbuk National Univ., Jeonju 561-756, Korea
    d Dep. of Agronomy and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108
    b Dep. of Crop and Soil Science, Oregon State Univ., Corvallis, OR 97331-3002
    c Instituto de Investigaciones Agropecuarias INIA, CRI-Quilamapu, Casilla 426, Chillan, Chile
    e Dep. of Plant Pathology, Univ. of Minnesota, St. Paul, MN 55108

Abstract

Foliar diseases of barley (Hordeum vulgare L.) such as spot blotch [caused by Cochliobolus sativus (Ito & Kuribayashi) Drechs. ex Dastur], net type net blotch (NTNB; caused by Pyrenophora teres f teres Drechs), Septoria speckled leaf blotch (SSLB; caused by Septoria passerinii Sacc.), leaf scald [caused by Rhynchosporium secalis (Oudem.) J. J. Davis], and powdery mildew (caused by Blumeria graminis f. sp. hordei Em. Marchal) can result in significant yield reductions in many production areas. The wild progenitor of cultivated barley, Hordeum vulgare subsp. spontaneum is well known as a rich source of disease resistance. To determine the location of H. vulgare subsp. spontaneum-derived alleles for disease resistance, we conducted quantitative trait locus (QTL) analysis of a recombinant inbred line (RIL) population derived from a cross between the resistant H. vulgare subsp. spontaneum accession OUH602 and the two-rowed malting cultivar Harrington. A total of 151 simple sequence repeats (SSR) markers were mapped into 11 linkage groups, covering 948 cM. Major QTLs for resistance to each disease were identified: one for spot blotch resistance on chromosome 1(7H); three for NTNB resistance on chromosomes 3(3H), 4(4H), and 5(1H); two for SSLB resistance on chromosomes 2(2H) and 6(6H); one for leaf scald resistance on chromosome 5(1H); and two for powdery mildew resistance on chromosomes 4(4H) and 5(1H). Resistance alleles for each QTL were contributed by OUH602, except those for NTNB and powdery mildew resistance on chromosome 5(1H) and chromosome 4(4H), respectively. The two QTLs identified for SSLB resistance are novel. All other QTLs mapped to regions where known resistance QTLs or major resistance genes have been reported. Our results indicate that most of the OUH602-derived loci are clustered in regions coincident with those described in cultivated barley. These resistance QTLs and their associated markers should be valuable for further exploitation of disease resistance variation in barley improvement.

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