Singh Davinder, Ziems Laura, Chettri Mumta, Dracatos Peter, Forrest Kerrie, Bhavani Sridhar, Singh Ravi, Barnes Charles W, Zapata Patricio Javier Noroña, Gangwar Om, Kumar Subodh, Bhardwaj Subhash, Park Robert F
Plant Breeding Institute, School of Life and Environmental Sciences, University of Sydney, Cobbitty, NSW, Australia.
La Trobe Institute of Sustainable Agriculture & Food (LISAF), Department of Animal, Plant and Soil Sciences, AgriBio, Bundoora, VIC, Australia.
Front Plant Sci. 2024 Jul 19;15:1352402. doi: 10.3389/fpls.2024.1352402. eCollection 2024.
Barley stripe or yellow rust (BYR) caused by f. sp. () is a significant constraint to barley production. The disease is best controlled by genetic resistance, which is considered the most economical and sustainable component of integrated disease management. In this study, we assessed the diversity of resistance to in a panel of international barley genotypes (n = 266) under multiple disease environments (Ecuador, India, and Mexico) using genome-wide association studies (GWASs). Four quantitative trait loci (QTLs) (three on chromosome 1H and one on 7H) associated with resistance to were identified. The QTLs were validated by mapping resistance to in five biparental populations, which detected key genomic regions on chromosomes 1H (populations Pompadour/Zhoungdamei, Pompadour/Zug161, and CI9214/Baudin), 3H (Ricardo/Gus), and 7H (Fumai8/Baronesse). The QTL detected by GWAS and detected using biparental mapping populations co-located were the most consistent and stable across environments and are likely the same resistance region. was saturated using population CI9214/Baudin by enriching the target region, which placed the resistance locus between 7.9 and 8.1 Mbp (flanked by markers , 0.7 cM proximal to and , 3.2 cM distal on 1HS) in the Morex reference genome v.2. A Kompetitive Allele Specific PCR (KASP) marker that co-segregated for was developed. The marker was validated on 50 Australian barley cultivars, showing well-defined allelic discrimination and presence in six genotypes (Baudin, Fathom, Flagship, Grout, Sakurastar, and Shepherd). This marker can be used for reliable marker-assisted selection and pyramiding of resistance to and in diversifying the genetic base of resistance to stripe rust.
由条形柄锈菌大麦专化型(Puccinia striiformis f. sp. hordei)引起的大麦条锈病或黄锈病是大麦生产的一个重大限制因素。该病最好通过遗传抗性来控制,遗传抗性被认为是综合病害管理中最经济和可持续的组成部分。在本研究中,我们利用全基因组关联研究(GWAS),在多个病害环境(厄瓜多尔、印度和墨西哥)下评估了一组国际大麦基因型(n = 266)对条锈病的抗性多样性。鉴定出了4个与条锈病抗性相关的数量性状位点(QTL)(3个在1H染色体上,1个在7H染色体上)。通过在5个双亲群体中定位条锈病抗性对这些QTL进行了验证,这些群体在1H染色体(Pompadour/周大麦、Pompadour/Zug161和CI_{}9214/巴丁群体)、3H染色体(里卡多/古斯群体)和7H染色体(福麦8/巴罗内塞群体)上检测到了关键基因组区域。GWAS检测到的QTL和双亲定位群体检测到的QTL共定位,在不同环境中最为一致和稳定,可能是相同的抗性区域。利用CI_{}9214/巴丁群体通过富集目标区域对该QTL进行了饱和定位,在Morex参考基因组v.2中将抗性位点定位在7.9至8.1 Mbp之间(两侧为标记,在1HS上,与标记距离近端0.7 cM,与标记距离远端3.2 cM)。开发了一个与该QTL共分离的竞争性等位基因特异性PCR(KASP)标记。该标记在50个澳大利亚大麦品种上进行了验证,显示出明确的等位基因区分,并且在6个基因型(巴丁、法索姆、旗舰、格鲁特、樱之星和谢泼德)中存在。该标记可用于可靠的标记辅助选择和条锈病抗性聚合,并使条锈病抗性的遗传基础多样化。