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首页> 外文期刊>Potato Research >High-Resolution Mapping of Two Broad-Spectrum Late Blight Resistance Genes from Two Wild Species of the Solanum circaeifolium Group
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High-Resolution Mapping of Two Broad-Spectrum Late Blight Resistance Genes from Two Wild Species of the Solanum circaeifolium Group

机译:茄科植物两个野生物种的两个广谱晚疫病抗性基因的高分辨率定位

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High levels of resistance to Phytophthora infestans in Solanum are predominantly based on the gene-for-gene interaction. Identification of hitherto unknown R genes is essential for future pyramiding approaches. This could be achieved either through classic introgression breeding or through cisgenesis and could lead to sustainable control of late blight. Here, we report on the mapping of Rpi-cap1 and Rpi-qum1, two late blight R genes identified in the wild species Solanum capsicibaccatum and Solanum circaeifolium ssp. quimense, respectively, to very similar positions on the long arm of chromosome 11. Despite the difficulties encountered for marker development, a high-resolution genetic map with cleaved amplified polymorphic sequence markers was constructed. Furthermore, an R gene cluster-directed profiling approach led to the development of markers that closely linked to or co-segregated with the Rpi-cap1 gene. Both R genes are hypothesized to be homologous to the N gene, a toll-interleukin1 receptor–nucleotide-binding site–leucine-rich repeat domain type of R gene to tobacco mosaic virus from tobacco. To confirm this hypothesis, cloning of Rpi-cap1 and Rpi-qum1 should be pursued. Cloning would also be instrumental to facilitate the introduction of these valuable R genes into potato crops using cisgenic- and marker-assisted breeding approaches.
机译:茄属植物对疫霉菌的高水平抗性主要基于基因对基因的相互作用。迄今为止未知的R基因的鉴定对于未来的金字塔方法至关重要。这可以通过经典的基因渗入育种或通过同基因发生来实现,并且可以导致对晚疫病的可持续控制。在这里,我们报告了Rpi-cap1和Rpi-qum1的定位,这两个是在野生物种茄形茄和茄形蓝藻中鉴定的两个晚疫病R基因。分别位于11号染色体长臂上的非常相似的位置。尽管遇到了标记开发方面的困难,但仍构建了具有裂解的扩增多态序列标记的高分辨率遗传图谱。此外,R基因簇定向分析方法导致了与Rpi-cap1基因紧密连接或共分离的标记的发展。假设这两个R基因都与N基因同源,后者是R基因与烟草花叶病毒中的收费白细胞介素1受体-核苷酸结合位点-富含亮氨酸的重复结构域类型。为了证实该假设,应该进行Rpi-cap1和Rpi-qum1的克隆。克隆也将有助于使用顺生和标记辅助育种方法将这些有价值的R基因引入马铃薯作物。

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