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Dissection of Resistance Genes to Pseudomonas syringae pv. phaseolicola in UI3 Common Bean Cultivar

机译:对丁香假单胞菌抗性基因的剖析。 UI3普通豆品种中的菜豆

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摘要

Few quantitative trait loci have been mapped for resistance to Pseudomonas syringae pv. phaseolicola in common bean. Two F2 populations were developed from the host differential UI3 cultivar. The objective of this study was to further characterize the resistance to races 1, 5, 7 and 9 of Psp included in UI3. Using a QTL mapping approach, 16 and 11 main-effect QTLs for pod and primary leaf resistance were located on LG10, explaining up to 90% and 26% of the phenotypic variation, respectively. The homologous genomic region corresponding to primary leaf resistance QTLs detected tested positive for the presence of resistance-associated gene cluster encoding nucleotide-binding and leucine-rich repeat (NL), Natural Resistance Associated Macrophage (NRAMP) and Pentatricopeptide Repeat family (PPR) proteins. It is worth noting that the main effect QTLs for resistance in pod were located inside a 3.5 Mb genomic region that included the Phvul.010G021200 gene, which encodes a protein that has the highest sequence similarity to the RIN4 gene of Arabidopsis, and can be considered an important candidate gene for the organ-specific QTLs identified here. These results support that resistance to Psp from UI3 might result from the immune response activated by combinations of R proteins, and suggest the guard model as an important mechanism in pod resistance to halo blight. The candidate genes identified here warrant functional studies that will help in characterizing the actual defense gene(s) in UI3 genotype.
机译:很少有数量性状基因座被定位为对丁香假单胞菌PV的抗性。菜豆中的菜豆。从宿主的差异UI3品种开发了两个F2种群。这项研究的目的是进一步表征UI3中包含的Psp的第1、5、7和9号种族的抗性。使用QTL定位方法,在LG10上定位了16个和11个主要的荚果和初级叶片抗性QTL,分别解释了多达90%和26%的表型变异。检测到的与初级叶片抗性QTL对应的同源基因组区域检测到与编码核苷酸结合和富亮氨酸重复序列(NL),天然抗性相关巨噬细胞(NRAMP)和五肽肽重复序列家族(PPR)蛋白的抗性相关基因簇呈阳性。值得注意的是,荚果抗性的主要QTL位于3.5 Mb基因组区域内,其中包括Phvul.010G021200基因,该基因编码的蛋白与拟南芥的RIN4基因具有最高的序列相似性,可以认为是是此处鉴定的器官特异性QTL的重要候选基因。这些结果支持UI3对Psp的抗药性可能是由R​​蛋白的组合激活的免疫反应引起的,并表明了保护模型是荚果抗白叶枯病的重要机制。此处鉴定的候选基因需要进行功能研究,这将有助于表征UI3基因型中的实际防御基因。

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