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首页> 外文期刊>Frontiers in Plant Science >Genetic, Physical and Comparative Mapping of the Powdery Mildew Resistance Gene Pm21 Originating from Dasypyrum villosum
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Genetic, Physical and Comparative Mapping of the Powdery Mildew Resistance Gene Pm21 Originating from Dasypyrum villosum

机译:源自 Dasypyrum villosum 的白粉病抗性基因 Pm21 的遗传,物理和比较图谱

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摘要

Pm21 , originating from wheat wild relative Dasypyrum villosum , confers immunity to all known races of Blumeria graminis f. sp. tritici ( Bgt ) and has been widely utilized in wheat breeding. However, little is known on the genetic basis of the Pm21 locus. In the present study, four seedling-susceptible D. villosum lines (DvSus-1 ~ DvSus-4) were identified from different natural populations. Based on the collinearity among genomes of Brachypodium distachyon, Oryza , and Triticeae , a set of 25 gene-derived markers were developed declaring the polymorphisms between DvRes-1 carrying Pm21 and DvSus-1. Fine genetic mapping of Pm21 was conducted by using an extremely large F_(2)segregation population derived from the cross DvSus-1/DvRes-1. Then Pm21 was narrowed to a 0.01-cM genetic interval defined by the markers 6VS-08.4b and 6VS-10b. Three DNA markers, including a resistance gene analog marker, were confirmed to co-segregate with Pm21 . Moreover, based on the susceptible deletion line Y18-S6 induced by ethyl methanesulfonate treatment conducted on Yangmai 18, Pm21 was physically mapped into a similar interval. Comparative analysis revealed that the orthologous regions of the interval carrying Pm21 were narrowed to a 112.5 kb genomic region harboring 18 genes in Brachypodium , and a 23.2 kb region harboring two genes in rice, respectively. This study provides a high-density integrated map of the Pm21 locus, which will contribute to map-based cloning of Pm21 .
机译:Pm21源自小麦野生近缘种(Dasypyrum villosum),可赋予所有已知的Blumeria graminis f。小种免疫力。 sp。 Tritici(Bgt),已被广泛用于小麦育种。但是,关于Pm21基因座的遗传基础知之甚少。在本研究中,从不同的自然种群中鉴定出了四个对幼苗敏感的绒毛线虫DvSus-1〜DvSus-4。基于曲霉菌,稻和小麦的基因组之间的共线性,开发了一组25个基因衍生标记,表明携带Pm21的DvRes-1和DvSus-1之间的多态性。通过使用来自交叉DvSus-1 / DvRes-1的非常大的F_(2)隔离种群,对Pm21进行了精细的遗传定位。然后将Pm21缩小到标记6VS-08.4b和6VS-10b定义的0.01-cM遗传间隔。证实了三个DNA标记,包括抗性基因类似物标记,与Pm21共分离。此外,基于在Yangmai 18上进行的甲磺酸乙酯处理诱导的易感缺失线Y18-S6,将Pm21物理映射到相似的区间。对比分析显示,携带Pm21的间隔的直系同源区分别缩小到了在稻草中含有18个基因的112.5 kb基因组区域和在水稻中含有两个基因的23.2 kb基因区域。这项研究提供了Pm21基因座的高密度整合图谱,这将有助于基于图谱的Pm21克隆。

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