Molecular mapping of an adult plant stem rust resistance gene Sr56 in winter wheat cultivar Arina

被引:62
作者
Bansal, Urmil [1 ]
Bariana, Harbans [1 ]
Wong, Debbie [2 ]
Randhawa, Mandeep [1 ]
Wicker, Thomas [3 ]
Hayden, Matthew [2 ]
Keller, Beat [3 ]
机构
[1] Univ Sydney Plant Breeding Inst Cobbitty, Narellan, NSW 2567, Australia
[2] AgriBiosci Ctr, Dept Environm & Primary Ind, Bundoora, Vic 3082, Australia
[3] Univ Zurich, Inst Plant Biol, CH-8008 Zurich, Switzerland
关键词
BREAD WHEAT; MAP; SELECTION; IDENTIFICATION; SOFTWARE; MARKERS; UG99;
D O I
10.1007/s00122-014-2311-1
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
This article covers detailed characterization and naming of QSr.sun - 5BL as Sr56 . Molecular markers linked with adult plant stem rust resistance gene Sr56 were identified and validated for marker-assisted selection. The identification of new sources of adult plant resistance (APR) and effective combinations of major and minor genes is well appreciated in breeding for durable rust resistance in wheat. A QTL, QSr.sun-5BL, contributed by winter wheat cultivar Arina providing 12-15 % reduction in stem rust severity, was reported in an Arina/Forno recombinant inbred line (RIL) population. Following the demonstration of monogenic segregation for APR in the Arina/Yitpi RIL population, the resistance locus was formally named Sr56. Saturation mapping of the Sr56 region using STS (from EST and DArT clones), SNP (9 K) and SSR markers from wheat chromosome survey sequences that were ordered based on synteny with Brachypodium distachyon genes in chromosome 1 resulted in the flanking of Sr56 by sun209 (SSR) and sun320 (STS) at 2.6 and 1.2 cM on the proximal and distal ends, respectively. Investigation of conservation of gene order between the Sr56 region in wheat and B. distachyon showed that the syntenic region defined by SSR marker interval sun209-sun215 corresponded to approximately 192 kb in B. distachyon, which contains five predicted genes. Conservation of gene order for the Sr56 region between wheat and Brachypodium, except for two inversions, provides a starting point for future map-based cloning of Sr56. The Arina/Forno RILs carrying both Sr56 and Sr57 exhibited low disease severity compared to those RILs carrying these genes singly. Markers linked with Sr56 would be useful for marker-assisted pyramiding of this gene with other major and APR genes for which closely linked markers are available.
引用
收藏
页码:1441 / 1448
页数:8
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