Department of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA.
Theor Appl Genet. 2013 May;126(5):1179-88. doi: 10.1007/s00122-013-2045-5. Epub 2013 Feb 3.
Wheat production is currently threatened by widely virulent races of the wheat stem rust fungus, Puccinia graminis f. sp. tritici, that are part of the TTKSK (also known as 'Ug99') race group. The diploid D genome donor species Aegilops tauschii (2n = 2x = 14, DD) is a readily accessible source of resistance to TTKSK and its derivatives that can be transferred to hexaploid wheat, Triticum aestivum (2n = 6x = 42, AABBDD). To expedite transfer of TTKSK resistance from Ae. tauschii, a direct hybridization approach was undertaken that integrates gene transfer, mapping, and introgression into one process. Direct crossing of Ae. tauschii accessions with an elite wheat breeding line combines the steps of gene transfer and introgression while development of mapping populations during gene transfer enables the identification of closely linked markers. Direct crosses were made using TTKSK-resistant Ae. tauschii accessions TA1662 and PI 603225 as males and a stem rust-susceptible T. aestivum breeding line, KS05HW14, as a female. Embryo rescue enabled recovery of F1 (ABDD) plants that were backcrossed as females to the hexaploid recurrent parent. Stem rust-resistant BC1F1 plants from each Ae. tauschii donor source were used as males to generate BC2F1 mapping populations. Bulked segregant analysis of BC2F1 genotypes was performed using 70 SSR loci distributed across the D genome. Using this approach, stem rust resistance genes from both accessions were located on chromosome arm 1DS and mapped using SSR and EST-STS markers. An allelism test indicated the stem rust resistance gene transferred from PI 603225 is Sr33. Race specificity suggests the stem rust resistance gene transferred from TA1662 is unique and this gene has been temporarily designated SrTA1662. Stem rust resistance genes derived from TA1662 and PI 603225 have been made available with selectable molecular markers in genetic backgrounds suitable for stem rust resistance breeding.
小麦生产目前受到广泛流行的小麦秆锈病菌(Puccinia graminis f. sp. tritici)的威胁,该病菌是 TTKSK(也称为“Ug99”)菌系群的一部分。二倍体 D 基因组供体物种节节麦(2n = 2x = 14,DD)是 TTKSK 及其衍生物的一种易于获得的抗性来源,可以转移到六倍体小麦普通小麦(2n = 6x = 42,AABBDD)中。为了加快从节节麦中转移 TTKSK 抗性,采用了直接杂交方法,将基因转移、图谱绘制和基因渗入整合到一个过程中。节节麦品系与一个优秀的小麦育种系的直接杂交结合了基因转移和基因渗入的步骤,而在基因转移过程中开发图谱群体可鉴定紧密连锁的标记。直接杂交使用 TTKSK 抗性节节麦品系 TA1662 和 PI 603225 作为雄性,而将感秆锈病的普通小麦育种系 KS05HW14 作为雌性。胚拯救使获得了 F1(ABDD)植物,然后将其作为雌性回交至六倍体轮回亲本。从每个节节麦供体来源获得的抗秆锈病 BC1F1 植物被用作雄性,以生成 BC2F1 图谱群体。使用分布在 D 基因组上的 70 个 SSR 标记对 BC2F1 基因型进行了 bulked segregant 分析。使用这种方法,从两个品系中定位了来自染色体臂 1DS 的秆锈病抗性基因,并使用 SSR 和 EST-STS 标记进行了图谱绘制。等位基因测试表明,从 PI 603225 转移的秆锈病抗性基因是 Sr33。品种特异性表明,从 TA1662 转移的秆锈病抗性基因是独特的,该基因暂时被命名为 SrTA1662。来自 TA1662 和 PI 603225 的抗秆锈病基因已在遗传背景中提供了可选择的分子标记,这些遗传背景适合抗秆锈病育种。