Hu Wenjing, Zhang Xiao, Zhu Dongmei, Zhao Die, Yong Rui, You Junchao, Zhang Yong, Gao Derong
Lixiahe Institute of Agriculture Sciences, Key Laboratory of Wheat Biology and Genetic Improvement for Low & Middle Yangtze Valley, Ministry of Agriculture and Rural Affairs, Yangzhou, 225007, Jiangsu, China.
Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops /Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Theor Appl Genet. 2025 Jun 12;138(7):150. doi: 10.1007/s00122-025-04936-6.
A novel Fusarium head blight resistance locus, QFhb-3BL, was identified and fine-mapped in common wheat. Identification and utilization of major resistance genes is key to developing new wheat cultivars/lines with improved Fusarium head blight (FHB) resistance. In this study, a moderately FHB-resistant cultivar Yangmai 16.2 (YM16.2) was crossed with a susceptible cultivar Yanzhan 1 (YZ1) to create a recombinant inbred line (RIL) population. Using bulk segregant analysis sequencing (BSA-seq) and linkage analysis, a new FHB quantitative trait locus (QTL) named QFhb-3BL, contributed by YM16.2, was identified. Eight Kompetitive Allele-Specific PCR (KASP) markers were used to detect homozygous recombinants in the derived lines of the remaining heterozygous line (RHL). QFhb-3BL was finely mapped to the 751.10-756.45 Mb interval, which contains 75 high-confidence genes. Through variation analysis of the candidate region and RNA sequencing (RNA-seq), we identified 11 genes with sequence variations and 14 genes expressed within the fine-mapping interval, with four genes overlapping between the two groups. KASP markers for the candidate gene TraesCS3B03G1226500 were validated in 103 wheat cultivars/lines, and lines carrying these markers showed a 38.89% reduction in FHB severity. This study provides a foundation for QFhb-3BL cloning and an effective marker for FHB resistance breeding.
在普通小麦中鉴定并精细定位了一个新的赤霉病抗性位点QFhb-3BL。鉴定和利用主要抗性基因是培育具有改良赤霉病(FHB)抗性的小麦新品种/品系的关键。在本研究中,将一个中度抗FHB的品种扬麦16.2(YM16.2)与一个感病品种偃展1号(YZ1)杂交,构建了一个重组自交系(RIL)群体。利用混合分组分析法测序(BSA-seq)和连锁分析,鉴定出一个由YM16.2贡献的新的FHB数量性状位点(QTL),命名为QFhb-3BL。使用8个竞争性等位基因特异性PCR(KASP)标记检测剩余杂合系(RHL)衍生系中的纯合重组体。QFhb-3BL被精细定位到751.10-756.45 Mb区间,该区间包含75个高可信度基因。通过对候选区域的变异分析和RNA测序(RNA-seq),我们鉴定出11个具有序列变异的基因和14个在精细定位区间内表达的基因,两组之间有4个基因重叠。对候选基因TraesCS3B03G1226500的KASP标记在103个小麦品种/品系中进行了验证,携带这些标记的品系FHB严重程度降低了38.89%。本研究为QFhb-3BL的克隆提供了基础,并为FHB抗性育种提供了一个有效的标记。