National Key Laboratory of Wheat Improvement, Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agriculture Sciences in Weifang, Weifang, 261325, Shandong, China.
Triticeae Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Theor Appl Genet. 2024 Apr 28;137(5):113. doi: 10.1007/s00122-024-04616-x.
The rust resistance genes Lr53 and Yr35 were introgressed into bread wheat from Aegilops longissima or Aegilops sharonensis or their S-genome containing species and mapped to the telomeric region of chromosome arm 6BS. Wheat leaf and stripe rusts are damaging fungal diseases of wheat worldwide. Breeding for resistance is a sustainable approach to control these two foliar diseases. In this study, we used SNP analysis, sequence comparisons, and cytogenetic assays to determine that the chromosomal segment carrying Lr53 and Yr35 was originated from Ae.longissima or Ae. sharonensis or their derived species. In seedling tests, Lr53 conferred strong resistance against all five Chinese Pt races tested, and Yr35 showed effectiveness against Pst race CYR34 but susceptibility to race CYR32. Using a large population (3892 recombinant gametes) derived from plants homozygous for the ph1b mutation obtained from the cross 98M71 × CSph1b, both Lr53 and Yr35 were successfully mapped to a 6.03-Mb telomeric region of chromosome arm 6BS in the Chinese Spring reference genome v1.1. Co-segregation between Lr53 and Yr35 was observed within this large mapping population. Within the candidate region, several nucleotide-binding leucine-rich repeat genes and protein kinases were identified as candidate genes. Marker pku6B3127 was completely linked to both genes and accurately predicted the absence or presence of alien segment harboring Lr53 and Yr35 in 87 tetraploid and 149 hexaploid wheat genotypes tested. We developed a line with a smaller alien segment (< 6.03 Mb) to reduce any potential linkage drag and demonstrated that it conferred resistance levels similar to those of the original donor parent 98M71. The newly developed introgression line and closely linked PCR markers will accelerate the deployment of Lr53 and Yr35 in wheat breeding programs.
将来自长穗偃麦草或节节麦及其含有 S 组基因组的物种的抗锈基因 Lr53 和 Yr35 导入普通小麦,并将其定位在 6BS 染色体臂的端粒区。小麦叶锈病和条锈病是全球范围内危害小麦的两种真菌病害。培育抗性是控制这两种叶部病害的可持续方法。在这项研究中,我们使用 SNP 分析、序列比较和细胞遗传学检测来确定携带 Lr53 和 Yr35 的染色体片段来源于长穗偃麦草或节节麦或其衍生物种。在幼苗试验中,Lr53 对所有测试的五个中国 Pst 小种均表现出强抗性,而 Yr35 对 Pst 小种 CYR34 表现出有效性,但对小种 CYR32 表现出敏感性。利用来自杂交 98M71 × CSph1b 的植物纯合 ph1b 突变体获得的 3892 个重组配子的大群体,成功地将 Lr53 和 Yr35 定位到中国春参考基因组 v1.1 中 6BS 染色体臂的 6.03-Mb 端粒区。在这个大的作图群体中观察到 Lr53 和 Yr35 之间的共分离。在候选区域内,鉴定出几个核苷酸结合亮氨酸丰富重复基因和蛋白激酶作为候选基因。标记 pku6B3127 与这两个基因完全连锁,并在 87 个四倍体和 149 个六倍体小麦基因型中准确预测了含有 Lr53 和 Yr35 的外来片段的存在或缺失。我们开发了一个含有较小外来片段(<6.03 Mb)的系,以减少任何潜在的连锁累赘,并证明它赋予了与原始供体亲本 98M71 相似的抗性水平。新开发的导入系和紧密连锁的 PCR 标记将加速 Lr53 和 Yr35 在小麦育种计划中的应用。