Phytopathology. 2007 Jun;97(6):668-73. doi: 10.1094/PHYTO-97-6-0668.
ABSTRACT Stripe rust, caused by Puccinia striiformis f. sp. hordei, is one of the most important diseases of barley in the south-central and western United States. Growing resistant cultivars is the best approach for controlling the disease. The barley genotype BBA 2890 has all-stage resistance against all races of P. striiformis f. sp. hordei (PSH) identified thus far in the United States. The resistance in BBA 2890 is controlled by a single recessive gene, rps1.a. The objectives of this study were to identify resistance gene analog polymorphism (RGAP) markers for the all-stage resistance gene rps1.a, to map the gene on a barley chromosome using chromosome-specific simple sequence repeat (SSR) markers, and to determine the presence or absence of the flanking RGAP markers for the gene in 24 barley genotypes. Seedlings of the parents and 200 F(8) recombinant inbred lines (RILs) were tested for resistance to pathogen races PSH-14, PSH-48, and PSH-54 in the greenhouse in 2005. Genomic DNA was extracted from the parents and 150 F(8) RILs. The RGAP technique was used to identify molecular markers for the rps1.a gene. Twelve primer pairs generating repeatable polymorphic bands were selected for genotyping the 150 F(8) RILs. A genetic linkage group was constructed for the resistance gene with 13 RGAP markers and four chromosome-specific SSR markers. The four SSR markers mapped the gene on the long arm of barley chromosome 3H. The closest RGAP marker for the resistant allele was within a genetic distance of 2.1 centimorgans (cM). The closest marker for the susceptible allele was 6.8 cM away from the locus. The two closest RGAP markers for the resistant allele detected polymorphisms in 67 and 71% of the 24 barley genotypes when used individually, and detected polymorphism in 88% of the genotypes when used in combination. This information should be useful in incorporating the resistance gene into barley cultivars and in pyramiding the gene with other resistance genes for superior stripe rust resistance.
条锈病由条形柄锈菌引起,是美国中南部和西部大麦的最重要病害之一。培育抗性品种是控制该病的最佳方法。大麦基因型 BBA 2890 对迄今为止在美国鉴定的所有条形柄锈菌小种均具有全生育期抗性。BBA 2890 中的抗性由单个隐性基因 rps1.a 控制。本研究的目的是鉴定 rps1.a 全生育期抗性基因的抗性基因类似物多态性(RGAP)标记,利用染色体特异性简单重复序列(SSR)标记将基因定位在大麦染色体上,并确定该基因在 24 个大麦基因型中的侧翼 RGAP 标记的存在或缺失。2005 年,在温室中用病原菌小种 PSH-14、PSH-48 和 PSH-54 对亲本和 200 个 F8 重组自交系(RIL)幼苗进行了抗性测试。从亲本和 150 个 F8 RIL 中提取基因组 DNA。使用 RGAP 技术鉴定 rps1.a 基因的分子标记。选择 12 对引物产生可重复的多态性条带,用于对 150 个 F8 RIL 进行基因分型。利用 13 个 RGAP 标记和 4 个染色体特异性 SSR 标记构建了抗性基因的遗传连锁群。四个 SSR 标记将该基因定位在大麦 3H 染色体的长臂上。抗性等位基因的最近 RGAP 标记在 2.1 厘摩(cM)的遗传距离内。易感等位基因的最近标记距离位点 6.8 cM。当单独使用时,两个最接近抗性等位基因的 RGAP 标记分别在 67%和 71%的 24 个大麦基因型中检测到多态性,当组合使用时,在 88%的基因型中检测到多态性。这些信息将有助于将抗性基因导入大麦品种,并与其他抗性基因一起聚合,以获得更高的条锈病抗性。