Genetic dissection of Fusarium head blight resistance in spring wheat cv. ‘Glenn’

被引:0
|
作者
Ahmed ElFatih A. ElDoliefy
Ajay Kumar
James A. Anderson
Karl D. Glover
Sujan Mamidi
Elias M. Elias
Raed Seetan
Mohammed S. Alamri
Shahryar F. Kianian
Suraj Sapkota
Andrew Green
Mohamed Mergoum
机构
[1] North Dakota State University,Department of Plant Sciences
[2] University of Minnesota,Department of Agronomy and Plant Genetics
[3] South Dakota State University,Department of Plant Sciences
[4] University of Georgia,Department of Crop and Soil Sciences and Institute of Plant Breeding, Genetics, and Genomics
[5] Griffin Campus,Department of Computer Science
[6] Slippery Rock University,Department of Food Sciences and Nutrition
[7] King Saud University,Cereal Disease Laboratory
[8] USDA-ARS,Department of Plant Molecular Biology, Agricultural Genetic Engineering Research Institute (AGERI)
[9] University of Minnesota,undefined
[10] Agricultural Research Center (ARC),undefined
来源
Euphytica | 2020年 / 216卷
关键词
Hard red spring wheat; Heading date; Molecular marker assisted breeding; Quantitative trait loci;
D O I
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中图分类号
学科分类号
摘要
Fusarium head blight (FHB) is a major disease of wheat in many wheat-growing regions affecting wheat yield and quality. Glenn is arguably the most FHB-resistant spring wheat cultivar in the USA. To decipher the genetics of FHB resistance in Glenn, a population of 112 recombinant inbred lines was developed from the cross Glenn × MN00261-4 and evaluated for various FHB related traits at multiple locations in two states (North Dakota and Minnesota) over 3 years. Quantitative trait loci (QTL) analysis detected 15 QTL for FHB resistance related traits and heading date (HD). One QTL for FHB incidence (INC; type I resistance), six QTL for FHB severity (SEV; type II resistance), one QTL for Fusarium damaged kernels (FDK; type IV resistance), four QTL for disease index (DI), and three QTL for HD were detected. Major QTL defined as those consistent across multiple environments and explaining > 10% of the phenotypic variation were detected on chromosomes 5BL, 6BS, and 7AS. They were associated with multiple FHB variables and HD. The stable 6BS QTL with a large effect for FHB SEV resistance corresponded to the Fhb2 gene in Sumai 3. In addition, potentially novel QTL were identified on 1AS, 5BL and 7DS. Our study showed that FHB resistance in the GM population was contributed by loci other than Fhb1. The major QTL detected for FHB resistance have potential for use in marker-assisted breeding for FHB resistance.
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