Identification and molecular tagging of a gene from PI 289824 conferring resistance to leaf rust (Puccinia triticina) in wheat

被引:20
|
作者
Obert, DE
Fritz, AK
Moran, JL
Singh, S
Rudd, JC
Menz, MA [1 ]
机构
[1] Texas A&M Univ, Inst Plant Genom & Biotechnol, Dept Soil & Crop Sci, College Stn, TX 77843 USA
[2] ARS, USDA, Small Grains & Potato Germplasm Res Unit, Aberdeen, ID 83210 USA
[3] Kansas State Univ, Dept Agron, Manhattan, KS 66506 USA
[4] Texas A&M Univ, Inst Plant Genom & Biotechnol, College Stn, TX 77843 USA
[5] Kansas State Univ, Dept Plant Pathol, Manhattan, KS 66506 USA
[6] Texas A&M Univ, Texas Agr Expt Stn, Amarillo, TX 79106 USA
关键词
wheat; leaf rust; resistance genes;
D O I
10.1007/s00122-005-1974-z
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Host-plant resistance is the most economically viable and environmentally responsible method of control for Puccinia triticina, the causal agent of leaf rust in wheat (Triticum aestivum L.). The identification and utilization of new resistance sources is critical to the continued development of improved cultivars as shifts in pathogen races cause the effectiveness of widely deployed genes to be short lived. The objectives of this research were to identify and tag new leaf rust resistance genes. Forty landraces from Afghanistan and Iran were obtained from the National Plant Germplasm System and evaluated under field conditions at two locations in Texas. PI 289824, a landrace from Iran, was highly resistant under field infection. Further evaluation revealed that PI 289824 is highly resistant to a broad spectrum of leaf rust races, including the currently prevalent races of leaf rust in the Great Plains area of the USA. Eight F-1 plants, 176 F-2 individuals and 139 F-2:3 families of a cross between PI 289824 and T112 (susceptible) were evaluated for resistance to leaf rust at the seedling stage. Genetic analysis indicated resistance in PI 289824 is controlled by a single dominant gene. The AFLP analyses resulted in the identification of a marker (P39 M48-367) linked to resistance. The diagnostic AFLP band was sequenced and that sequence information was used to develop an STS marker (TXW200) linked to the gene at a distance of 2.3 cM. The addition of microsatellite markers allowed the gene to be mapped to the short arm of Chromosome 5B. The only resistance gene to be assigned to Chr 5BS is Lr52. The Lr52 gene was reported to be 16.5 cM distal to Xgwm443 while the gene in PI 289824 mapped 16.7 cM proximal to Xgwm443. Allelism tests are needed to determine the relationship between the gene in PI 289824 and Lr52. If the reported map positions are correct, the gene in PI 289824 is unique.
引用
收藏
页码:1439 / 1444
页数:6
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