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首页> 外文期刊>TAG Theoretical and Applied Genetics >Using a limited mapping strategy to identify major QTLs for resistance to grapevine powdery mildew (Erysiphe necator) and their use in marker-assisted breeding
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Using a limited mapping strategy to identify major QTLs for resistance to grapevine powdery mildew (Erysiphe necator) and their use in marker-assisted breeding

机译:使用有限的作图策略来鉴定对葡萄白粉病(Erysiphe necator)具有抗性的主要QTL及其在标记辅助育种中的用途

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摘要

A limited genetic mapping strategy based on simple sequence repeat (SSR) marker data was used with five grape populations segregating for powdery mildew (Erysiphe necator) resistance in an effort to develop genetic markers from multiple sources and enable the pyramiding of resistance loci. Three populations derived their resistance from Muscadinia rotundifolia ‘Magnolia’. The first population (06708) had 97 progeny and was screened with 137 SSR markers from seven chromosomes (4, 7, 9, 12, 13, 15, and 18) that have been reported to be associated with powdery or downy mildew resistance. A genetic map was constructed using the pseudo-testcross strategy and QTL analysis was carried out. Only markers from chromosome 13 and 18 were mapped in the second (04327) and third (06712) populations, which had 47 and 80 progeny, respectively. Significant QTLs for powdery mildew resistance with overlapping genomic regions were identified for different tissue types (leaf, stem, rachis, and berry) on chromosome 18, which distinguishes the resistance in ‘Magnolia’ from that present in other accessions of M. rotundifolia and controlled by the Run1 gene on chromosome 12. The ‘Magnolia’ resistance locus was termed as Run2.1. Powdery mildew resistance was also mapped in a fourth population (08391), which had 255 progeny and resistance from M. rotundifolia ‘Trayshed’. A locus accounting for 50% of the phenotypic variation mapped to chromosome 18 and was named Run2.2. This locus overlapped the region found in the ‘Magnolia’-based populations, but the allele sizes of the flanking markers were different. ‘Trayshed’ and ‘Magnolia’ shared at least one allele for 68% of the tested markers, but alleles of the other 32% of the markers were not shared indicating that the two M. rotundifolia selections were very different. The last population, 08306 with 42 progeny, derived its resistance from a selection Vitis romanetii C166-043. Genetic mapping discovered a major powdery mildew resistance locus termed Ren4 on chromosome 18, which explained 70% of the phenotypic variation in the same region of chromosome 18 found in the two M. rotundifolia resistant accessions. The mapping results indicate that powdery mildew resistance genes from different backgrounds reside on chromosome 18, and that genetic markers can be used as a powerful tool to pyramid these loci and other powdery mildew resistance loci into a single line.
机译:基于简单序列重复(SSR)标记数据的有限遗传作图策略与五个葡萄种群隔离,用于白粉病(Erysiphe necator)抗性,以努力从多个来源开发遗传标记并实现抗性基因座的金字塔化。三个种群的抵抗来自圆叶锦葵(Muscadinia rotundifolia)“木兰”。第一批(06708)具有97个后代,并用来自七个染色体(4、7、9、12、13、15和18)的137个SSR标记进行了筛选,据报道这些染色体与白粉病或霜霉病抗性相关。使用伪testcross策略构建了遗传图谱,并进行了QTL分析。仅来自第13和18号染色体的标记被定位在第二个(04327)和第三个(06712)种群中,它们分别具有47和80个后代。在18号染色体上针对不同组织类型(叶,茎,叶轴和浆果)鉴定了具有重叠基因组区域的白粉病抗性的重要QTL,这将'木兰'的抗性与轮枝分枝杆菌其他种和对照中的抗性区分开由12号染色体上的Run1基因决定。“木兰”抗性基因座称为Run2.1。白粉病抗性也定位于第四种群(08391),其具有255个后代和轮状支原体“托盘”的抗性。占表型变异50%的基因座定位于18号染色体,命名为Run2.2。该基因座与基于“木兰”的种群中发现的区域重叠,但侧翼标记的等位基因大小不同。 “ Trayshed”和“ Magnolia”在68%的测试标记中共享至少一个等位基因,但是其他32%的标记的等位基因没有共享,这表明轮枝分枝杆菌的两个选择非常不同。最后一个种群,具有42个后代的08306,来自对罗马葡萄C166-043的选择。遗传作图发现在18号染色体上有一个主要的白粉病抗性基因座,称为Ren4,这解释了在两个圆叶分枝杆菌抗性种质中发现的18号染色体同一区域中70%的表型变异。该作图结果表明,来自不同背景的白粉病抗性基因位于第18号染色体上,并且遗传标记可以用作将这些基因座和其他白粉病抗性基因座金字塔化成一条线的有力工具。

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