Wang Chenxi, Bai Jiaxing, Xiong Hongchun, Xie Yongdun, Gu Jiayu, Zhao Linshu, Li Huiyuan, Ding Yuping, Guo Xinmei, Guo Huijun, Liu Luxiang
College of Life Sciences, Key Laboratory of Major Crop Germplasm Innovation and Application in Qingdao, Qingdao Agricultural University, Qingdao, China.
State Key Laboratory of Crop Gene Resources and Breeding/National Engineering Laboratory of Crop Molecular Breeding/CAEA Research and Development Centre on Nuclear Technology Applications for Irradiation Mutation Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, China.
Plant Genome. 2025 Jun;18(2):e70043. doi: 10.1002/tpg2.70043.
Tiller number is a crucial determinant of grain yield in wheat (Triticum aestivum L.), and identifying functional alleles can enhance our understanding of wheat tiller development. Here, we describe the ot2 wheat mutant, which exhibits a 91% reduction in tiller number compared to the wild type and displays inhibited tiller bud differentiation from the 2-3 leaf stage. Bulked segregant analysis combined with exon sequencing mapped the Taot2 gene to chromosome 1BL. Fourteen kompetitive allele-specific PCR markers were developed and utilized to narrow down the region containing Taot2 to a 2.22 Mb interval. This region encompasses 39 high-confidence genes. Through transcriptomic analysis and functional gene investigation, TraesCS1B03G1126300 was identified as the candidate gene, encoding an auxin-responsive protein of the auxin/indole-3-acetic acid family. Our findings provide the foundation for map-based cloning of Taot2, a novel wheat tiller gene, and offer valuable insights into wheat tiller bud initiation.
分蘖数是小麦(Triticum aestivum L.)产量的关键决定因素,鉴定功能等位基因有助于我们加深对小麦分蘖发育的理解。在此,我们描述了ot2小麦突变体,与野生型相比,其分蘖数减少了91%,并且从2-3叶期开始表现出分蘖芽分化受到抑制。混合分组分析法结合外显子测序将Taot2基因定位到1BL染色体上。开发并利用了14个竞争性等位基因特异性PCR标记,将包含Taot2的区域缩小到2.22 Mb的区间。该区域包含39个高可信度基因。通过转录组分析和功能基因研究,确定TraesCS1B03G1126300为候选基因,它编码一种生长素/吲哚-3-乙酸家族的生长素响应蛋白。我们的研究结果为基于图谱克隆新型小麦分蘖基因Taot2奠定了基础,并为小麦分蘖芽起始提供了有价值的见解。