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首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Simultaneous transfer, introgression, and genomic localization of genes for resistance to stem rust race TTKSK (Ug99) from Aegilops tauschii to wheat.
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Simultaneous transfer, introgression, and genomic localization of genes for resistance to stem rust race TTKSK (Ug99) from Aegilops tauschii to wheat.

机译:同时对tauschii小麦到小麦的茎锈病TTKSK(Ug99)抗性基因的基因转移,基因渗入和基因组定位。

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摘要

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.
机译:目前,小麦茎锈病真菌Puccinia graminis f。的强毒种正在威胁小麦的生产。 sp。 Tritici,是TTKSK(也称为“ Ug99”)比赛组的一部分。二倍体D基因组供体物种Aegilops tauschii(2n = 2x = 14,DD)是一种易于获得的对TTKSK及其衍生物的抗性来源,可将其转移至六倍体小麦(Triticum aestivum)(2n = 6x = 42,AABBDD)。加快Ae对TTKSK耐药性的转移。 tauschii,采取了一种直接杂交的方法,将基因转移,作图和基因渗入整合到一个过程中。 Ae的直接交叉。 tauschii品系与优质小麦育种系相结合,融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作图种群可以鉴定紧密相连的标记。使用抗TTKSK的Ae直接杂交。 tauschii保藏号TA1662和PI 603225为雄性,茎锈病易感普通小麦育种系KS05HW14为雌性。胚胎抢救使F 1 (ABDD)植物得以恢复,这些植物作为雌性与六倍体轮回亲本回交。从每个Ae茎抗锈菌BC 1 F 1 植物。 tauschii供体来源被用作雄性以产生BC 2 F 1 作图种群。使用分布在D基因组中的70个SSR基因座,对BC 2 F 1 基因型进行了批量分离分析。使用这种方法,将来自两个种质的茎锈病抗性基因定位在1DS染色体臂上,并使用SSR和EST-STS标记进行定位。等位测试表明,从PI 603225转移过来的茎锈病抗性基因是Sr33。种族特异性表明,从TA1662转移来的茎锈病抗性基因是独特的,该基因已被临时命名为SrTA1662。从TA1662和PI 603225衍生而来的茎锈病抗性基因已在适用于茎锈病抗性育种的遗传背景中提供了带有可选分子标记的基因。

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