Crop Research Institute, Gansu Academy of Agricultural Sciences, Lanzhou, 730070, China.
College of Agronomy and Biotechnology, Southwest University, Chongqing, 400716, China.
Theor Appl Genet. 2024 Jan 31;137(2):39. doi: 10.1007/s00122-023-04524-6.
Two major genetic loci, qTN5.1 and qAB9.1, were identified and finely mapped to the 255 Kb region with one potential candidate gene for tiller number and the 521 Kb region with eight candidate genes for axillary branch number, respectively. Vegetative branching including tillering and axillary branching are vital traits affecting both the plant architecture and the biomass in cereal crops. However, the mechanism underlying the formation of vegetative branching in foxtail millet is largely unknown. Here, a foxtail millet cultivar and its bushy wild relative Setaria viridis accession were used to construct segregating populations to identify candidate genes regulating tiller number and axillary branch number. Transcriptome analysis using vegetative branching bud samples of parental accessions was performed, and key differentially expressed genes and pathways regulating vegetative branching were pointed out. Bulk segregant analysis on their F segregating population was carried out, and a major QTL for tiller number (qTN5.1) and two major QTLs for axillary branch number (qAB2.1 and qAB9.1) were detected. Fine-mapping strategy was further performed on F segregate population, and Seita.5G356600 encoding β-glucosidase 11 was identified as the promising candidate gene for qTN5.1, and eight genes, especially Seita.9G125300 and Seita.9G125400 annotated as B-S glucosidase 44, were finally identified as candidate genes for regulating axillary branching. Findings in this study will help to elucidate the genetic basis of the vegetative branching formation of foxtail millet and lay a foundation for breeding foxtail millet varieties with ideal vegetative branching numbers.
两个主要的遗传位点 qTN5.1 和 qAB9.1 被鉴定出来,并被精细地定位到 255 Kb 区域,该区域有一个潜在的分蘖数候选基因,以及 521 Kb 区域,该区域有 8 个腋芽数候选基因。营养分枝包括分蘖和腋芽分枝是影响谷类作物株型和生物量的重要性状。然而,谷子营养分枝形成的机制在很大程度上尚不清楚。在这里,利用谷子品种及其丛生野生近缘种柳枝稷构建分离群体,以鉴定调控分蘖数和腋芽数的候选基因。对亲本材料的营养分枝芽样品进行转录组分析,指出了调控营养分枝的关键差异表达基因和途径。对其 F 分离群体进行了混池分离分析,检测到一个分蘖数的主效 QTL(qTN5.1)和两个腋芽数的主效 QTL(qAB2.1 和 qAB9.1)。进一步在 F 分离群体中进行精细定位,鉴定到 Seita.5G356600 基因,该基因为 β-葡萄糖苷酶 11,是 qTN5.1 的候选基因,同时鉴定到 8 个基因,特别是 Seita.9G125300 和 Seita.9G125400,注释为 B-S 葡萄糖苷酶 44,为调控腋芽分枝的候选基因。本研究的结果将有助于阐明谷子营养分枝形成的遗传基础,并为培育理想分枝数的谷子品种奠定基础。