Agricultural Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, PO Box 19, 2462, Martonvasar, Hungary.
Nottingham BBSRC Wheat Research Centre, Division of Plant and Crop Sciences, School of Biosciences, Univ. of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD, UK.
Plant Genome. 2019 Nov;12(3):1-7. doi: 10.3835/plantgenome2018.12.0098.
We identified 1247 polymorphic single nucleotide polymorphisms between Triticum monococcum and wheat. We identified 191 markers validated across all seven chromosomes of T. monococcum. Detected a T. monococcum introgression in leaf-rust-resistant lines. Cultivated einkorn wheat (Triticum monococcum L. subsp. monococcum, 2n = 2x = 14, A A ) and its wild relative T. monococcum subsp. aegilopoides are important sources of economically useful genes that can be exploited for wheat (Triticum aestivum L.) breeding. Einkorn has excellent resistance to fungal diseases and gene transfer is relatively simple via standard breeding methods. To fulfill the growing demand by modern prebreeding programs for a cost-effective high-throughput procedure for accurately detecting introgressed chromosomes or chromosome segments from T. monococcum into wheat, we used the Axiom Wheat-Relative Genotyping Array and developed a set of A genome-specific exome-based single nucleotide polymorphism (SNP) markers suitable for rapid identification of T. monococcum chromatin in a wheat background. We identified 1247 polymorphic SNPs between T. monococcum and wheat. We identified 191 markers across all seven chromosomes of T. monococcum that are also present on an existing Triticum urartu Thum. ex Gandil. genetic map and potentially ordered them on the basis of the high macrocollinearity and conservation of marker order between T. monococcum and T. urartu. The marker set has been tested on leaf-rust-resistant BC F progenies of wheat-T. monococcum hybrids. Two markers (AX-94492165, AX-95073542) placed on the distal end of the chromosome arm 7AL detected a T. monococcum introgression into wheat. The SNP marker set thus proved highly effective in the identification of T. monococcum chromatin in a wheat background, offering a reliable method for screening and selecting wheat-T. monococcum introgression lines, a procedure that could significantly speed up prebreeding programs.
我们在一粒小麦和小麦之间鉴定了 1247 个多态性单核苷酸多态性。我们在七个染色体的所有七个染色体上鉴定了 191 个标记。在抗叶锈病系中检测到一粒小麦的渐渗。栽培单粒小麦(Triticum monococcum L. subsp. monococcum,2n = 2x = 14,A A )及其野生近缘种 T. monococcum subsp. aegilopoides 是经济有用基因的重要来源,可用于小麦(Triticum aestivum L.)的选育。单粒小麦对真菌病具有极好的抗性,并且通过标准育种方法基因转移相对简单。为了满足现代预育计划对经济高效的高通量程序的需求,以准确检测从一粒小麦到小麦的渐渗染色体或染色体片段,我们使用了 Axiom 小麦相关基因分型阵列,并开发了一套 A 基因组特异的基于外显子的单核苷酸多态性(SNP)标记,这些标记适合快速鉴定小麦背景中的一粒小麦染色质。我们在一粒小麦和小麦之间鉴定了 1247 个多态性 SNP。我们在七个染色体的所有七个染色体上鉴定了 191 个标记,这些标记也存在于现有的 Triticum urartu Thum. ex Gandil. 遗传图谱上,并且根据高宏基因组间的高度宏观基因组间和标记顺序的保守性,对其进行了排序。标记集已在小麦-一粒小麦杂种的抗叶锈病 BC F 后代上进行了测试。位于染色体臂 7AL 远端的两个标记(AX-94492165,AX-95073542)检测到一粒小麦的渐渗到小麦中。因此,SNP 标记集在小麦背景中鉴定一粒小麦染色质非常有效,为筛选和选择小麦-一粒小麦渐渗系提供了可靠的方法,这一过程可以显著加快预育计划的进程。