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Targeted molecular mapping of the adult plant resistance gene Lr46 in wheat and introgression into hard winter wheat adapted to Kansas.

机译:针对小麦的成年植物抗性基因Lr46的靶向分子作图,以及渗入适应堪萨斯州的硬冬小麦。

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Leaf rust (caused by Puccinia triticina Eriks) is a widespread fungal disease of wheat. Adult plant resistance gene Lr46 has provided effective resistance against diverse races of the pathogen for almost 30 years and is thought to be durable. Previous reports located QTL corresponding to Lr46 distally on wheat chromosome 1BL. We confirmed the linkage of 1BL markers with Lr46 in a single chromosome recombinant line population where Lr46 segregates as a single gene. Using Chinese Spring (CS) deletion stocks to map the linked SSR (simple sequence repeat) markers, we determined that Lr46 is likely present in the deletion bin 1BL 0.84--0.89. To increase marker density in this region, wheat expressed sequence tags (ESTs) that mapped in the terminal 15% of chromosome 1BL were used as queries in BLASTn searches against the rice genome sequence. Wheat ESTs with significant homology to sequences from the terminal region of chromosome 5L of rice were chosen for STS (sequence-tagged site) primer design and mapped physically and genetically. Once synteny in the region was confirmed, sequences from two BAC (bacterial artificial chromosome) clones covering the target syntenic region of rice 5L were used to identify additional wheat ESTs potentially linked to Lr46. By this method, 16 additional STS markers located in a small deletion bin comprising less than 1% of chromosome 1BL were developed. A total of eight STS markers could be mapped in two populations segregating for Lr46. Of these, two markers flanking Lr46 (3.0 cM proximal and 0.7 cM distal) were identified. The physical location of the gene was confined to a sub-microscopic deletion bin between breakpoints for deletion line 1BL-13 (0.89) and 1BL-4 (0.89). Introgression of Lr46 into hard winter wheat (HWW) germplasm adapted to Kansas was done by backcrossing. Molecular and phenotypic selections were used to develop BC2F4 lines with Lr46 in two different HWW backgrounds. After field evaluation in 2004--05, the best lines will be released as germplasm to wheat breeders. This work has resulted in a source of durable resistance in a winter wheat background and the markers for deployment of Lr46 by breeding programs.
机译:叶锈病(由小麦锈病引起)是一种广泛的小麦真菌病。成年植物抗性基因Lr46已经提供了对病原体不同种族的有效抗性近30年,并且被认为是持久的。先前的报道将QTL对应于小麦染色体1BL的远端Lr46。我们证实了1BL标记与Lr46在单个染色体重组株群体中的连锁,其中Lr46分离为单个基因。使用中国春季(CS)删除库存来映射链接的SSR(简单序列重复)标记,我们确定Lr46可能存在于删除区1BL 0.84--0.89中。为了增加该区域的标记密度,在BLASTn搜索中针对水稻基因组序列的查询中使用了位于1BL染色体15%末端的小麦表达序列标签(EST)。选择与来自水稻5L染色体末端区域的序列具有显着同源性的小麦EST进行STS(序列标记位点)引物设计,并进行物理和遗传定位。一旦确认该区域的同义性,就使用覆盖水稻5L目标同义性区域的两个BAC(细菌人工染色体)克隆的序列来鉴定可能与Lr46相关的其他小麦EST。通过这种方法,开发了位于包含小于1%染色体1BL的小缺失区的16个其他STS标记。总共八个STS标记可在两个针对Lr46的种群中作图。其中,鉴定了Lr46侧翼的两个标记(近端3.0 cM和远端0.7 cM)。该基因的物理位置被限制在删除线1BL-13(0.89)和1BL-4(0.89)的断点之间的亚显微删除位中。通过回交将Lr46导入适合堪萨斯州的硬冬小麦(HWW)种质。在两个不同的HWW背景中,使用分子和表型选择来开发带有Lr46的BC2F4品系。经过2004--05年的田间评估后,最好的品系将作为种质发布给小麦育种者。这项工作导致了冬小麦背景中的持久抗性来源,以及通过育种计划部署Lr46的标志。

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