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精细定位、物理图谱构建和大麦 Rrs2 抗穗发芽基因诊断标记的开发。

Fine mapping, physical mapping and development of diagnostic markers for the Rrs2 scald resistance gene in barley.

机构信息

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstr. 3, 06466, Gatersleben, Germany.

出版信息

Theor Appl Genet. 2009 Nov;119(8):1507-22. doi: 10.1007/s00122-009-1152-9. Epub 2009 Sep 25.

Abstract

The Rrs2 gene confers resistance to the fungal pathogen Rhynchosporium secalis which causes leaf scald, a major barley disease. The Rrs2 gene was fine mapped to an interval of 0.08 cM between markers 693M6_6 and P1D23R on the distal end of barley chromosome 7HS using an Atlas (resistant) x Steffi (susceptible) mapping population of 9,179 F(2)-plants. The establishment of a physical map of the Rrs2 locus led to the discovery that Rrs2 is located in an area of suppressed recombination within this mapping population. The analysis of 58 barley genotypes revealed a large linkage block at the Rrs2 locus extending over several hundred kb which is present only in Rrs2 carrying cultivars. Due to the lack of recombination in the mapping population and the presence of a Rrs2-specific linkage block, we assume a local chromosomal rearrangement (alien introgression or inversion) in Rrs2 carrying varieties. The variety analysis led to the discovery of eight SNPs which were diagnostic for the Rrs2 phenotype. Based on these SNPs diagnostic molecular markers (CAPS and pyrosequencing markers) were developed which are highly useful for marker-assisted selection in resistance gene pyramiding programmes for Rhynchosporium secalis resistance in barley.

摘要

Rrs2 基因赋予大麦对禾旋孢腔菌(Rhynchosporium secalis)的抗性,该基因可导致叶斑病(一种主要的大麦病害)。利用 Atlas(抗性)x Steffi(感病)9179 个 F2 植株的作图群体,将 Rrs2 基因精细定位到大麦 7HS 染色体末端标记 693M6_6 和 P1D23R 之间 0.08cM 的区间内。Rrs2 基因座的物理图谱的建立导致发现 Rrs2 位于该作图群体中重组受到抑制的区域内。对 58 个大麦基因型的分析表明,在含有 Rrs2 的品种中存在一个几百 kb 大小的大连锁块,该连锁块仅存在于携带 Rrs2 的品种中。由于在作图群体中缺乏重组以及存在 Rrs2 特异性连锁块,我们假设携带 Rrs2 的品种中存在局部染色体重排(外来渗入或倒位)。品种分析发现了 8 个与 Rrs2 表型相关的 SNP,这些 SNP 可用于鉴定 Rrs2 表型。基于这些 SNP,开发了用于 CAPS 和焦磷酸测序的分子标记(RSP1-Rrs2 共分离),这些标记可用于禾旋孢腔菌抗性的基因聚合的辅助选择。

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