State Key Laboratory of North China Crop Improvement and Regulation, Hebei Sub-Center for National Maize Improvement Center, College of Agronomy, Hebei Agricultural University, Baoding, 071001, Hebei, China.
State Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Theor Appl Genet. 2024 Apr 3;137(4):92. doi: 10.1007/s00122-024-04593-1.
A chromosome fragment influencing wheat heading and grain size was identified using mapping of m406 mutant. The study of TaFPF1 in this fragment provides more insights into wheat yield improvement. In recent years, wheat production has faced formidable challenges driven by rapid population growth and climate change, emphasizing the importance of improving specific agronomic traits such as heading date, spike length, and grain size. To identify potential genes for improving these traits, we screened a wheat EMS mutant library and identified a mutant, designated m406, which exhibited a significantly delayed heading date compared to the wild-type. Intriguingly, the mutant also displayed significantly longer spike and larger grain size. Genetic analysis revealed that a single recessive gene was responsible for the delayed heading. Surprisingly, a large 46.58 Mb deletion at the terminal region of chromosome arm 2DS in the mutant was identified through fine mapping and fluorescence in situ hybridization. Thus, the phenotypes of the mutant m406 are controlled by a group of linked genes. This deletion encompassed 917 annotated high-confidence genes, including the previously studied wheat genes Ppd1 and TaDA1, which could affect heading date and grain size. Multiple genes in this region probably contribute to the phenotypes of m406. We further investigated the function of TaFPF1 using gene editing. TaFPF1 knockout mutants showed delayed heading and increased grain size. Moreover, we identified the direct upstream gene of TaFPF1 and investigated its relationship with other important flowering genes. Our study not only identified more genes affecting heading and grain development within this deleted region but also highlighted the potential of combining these genes for improvement of wheat traits.
利用 m406 突变体的作图,鉴定出影响小麦抽穗和粒大小的染色体片段。该片段中 TaFPF1 的研究为提高小麦产量提供了更多的见解。近年来,由于人口快速增长和气候变化的推动,小麦生产面临着严峻的挑战,强调了改善特定农艺性状(如抽穗期、穗长和粒大小)的重要性。为了鉴定潜在的基因来改善这些性状,我们筛选了一个小麦 EMS 突变体文库,并鉴定出一个突变体,命名为 m406,与野生型相比,它的抽穗期明显延迟。有趣的是,该突变体还表现出明显更长的穗和更大的粒大小。遗传分析表明,一个单隐性基因负责延迟抽穗。令人惊讶的是,通过精细作图和荧光原位杂交,在突变体的 2DS 染色体臂末端区域发现了一个大的 46.58Mb 缺失。因此,突变体 m406 的表型受一组连锁基因的控制。该缺失包含 917 个注释的高可信度基因,包括先前研究过的小麦基因 Ppd1 和 TaDA1,它们可能影响抽穗期和粒大小。该区域的多个基因可能对 m406 的表型有贡献。我们进一步利用基因编辑研究了 TaFPF1 的功能。TaFPF1 敲除突变体表现出抽穗延迟和粒增大。此外,我们鉴定了 TaFPF1 的直接上游基因,并研究了其与其他重要开花基因的关系。我们的研究不仅在这个缺失区域内鉴定出更多影响抽穗和粒发育的基因,还强调了组合这些基因以提高小麦性状的潜力。