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Hessian fly resistance genes H16 and H17 are mapped to a resistance gene cluster in the distal region of chromosome 1AS in wheat

机译:粗麻蝇抗性基因H16和H17定位于小麦1AS染色体远端区域的抗性基因簇

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摘要

Hessian fly [Mayetiola destructor (Say)] is one of the major insect pests of wheat (Triticum aestivum L.) worldwide. Hessian fly (Hf)-resistance genes H16 and H17 were reported to condition resistance to Hf biotype L that is prevalent in many wheat-growing areas of eastern USA, and both of them were previously assigned to wheat chromosome 5A by their linkage to H9. The objectives in this study were to (1) map H16 and H17 independent of their linkage with H9 and (2) identify DNA markers that co-segregate with H16 or H17, and that are useful for selection of these genes in segregating populations and to combine these genes with other Hf-resistance genes in wheat cultivars. Contrary to previously reported locations, H16 and H17 did not show linkage with the molecular markers on chromosome 5A. Instead, both of them are linked with the molecular markers on the short arm of chromosome 1A (1AS). The simple sequence repeat (SSR) marker Xpsp2999 and EST-derived SSR (eSSR) marker Xwem6b are two flanking markers that are linked to H16 at genetic distances of 3.7 and 5.5 cM, respectively. Similarly, H17 is located between markers Xpsp2999 and Xwem6b at genetic distances of 6.2 and 5.1 cM, respectively. Five other SSR and eSSR markers including Xcfa2153, Xbarc263, Xwem3a, Xwmc329, and Xwmc24 were also linked to H16 and H17 at close genetic distances. These closely linked molecular markers should be useful for pyramiding H16 and H17 with other Hessian fly resistance genes in a single wheat genotype. In addition, using Chinese Spring deletion line bin mapping we positioned all of the linked markers and the Hf-resistance genes (H16 and H17) to the distal 14% of chromosome 1AS, where Hf-resistance genes H9, H10, and H11 are located. Our results together with previous studies suggest that Hf-resistance genes H9, H10, H11, H16, and H17 along with the pathogen resistance genes Pm3 and Lr10 appear to occupy a resistance gene cluster in the distal region of chromosome 1AS in wheat.
机译:粗麻布蝇[Mayetiola destructor(Say)]是全世界小麦(Triticum aestivum L.)的主要害虫之一。据报道,黑森州蝇(Hfs)抗性基因H16和H17调节了对Hf生物型L的抗性,这种抗性在美国东部许多小麦种植区普遍存在,并且由于它们与H9的连锁关系,它们都先前被分配给了小麦5A染色体。这项研究的目的是(1)绘制H16和H17与H9无关的图谱,以及(2)鉴定与H16或H17共分离的DNA标记,这些标记可用于选择分离群体中的这些基因,并将这些基因与小麦品种中的其他抗Hf基因融合在一起。与以前报道的位置相反,H16和H17没有显示出与5A染色体上的分子标记的联系。相反,它们都与1A号染色体(1AS)短臂上的分子标记相连。简单序列重复(SSR)标记Xpsp2999和EST衍生的SSR(eSSR)标记Xwem6b是两个侧翼标记,它们分别以3.7和5.5 cM的遗传距离与H16连接。同样,H17位于标记Xpsp2999和Xwem6b之间,遗传距离分别为6.2和5.1 cM。包括Xcfa2153,Xbarc263,Xwem3a,Xwmc329和Xwmc24在内的其他五个SSR和eSSR标记也以近遗传距离与H16和H17连锁。这些紧密联系的分子标记对于在单个小麦基因型中将H16和H17与其他Hessian蝇抗性基因金字塔化很有用。此外,使用中国春季删除线bin图谱,我们将所有链接的标记和Hf抗性基因(H16和H17)定位在1AS染色体14%的末端,Hf抗性基因H9,H10和H11位于此处。我们的结果以及以前的研究表明,Hf抗性基因H9,H10,H11,H16和H17以及病原体抗性基因Pm3和Lr10似乎在小麦1AS染色体的末端区域占据了抗性基因簇。

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