Dai Yintao, Yu Ningning, Xu Hongxing, Liu Shaoqing, Zhang Jiadong, Liu Ruishan, Li Jiatong, Li Yaoxue, Xiao Bei, Pan Guantong, Li Dongming, Liu Cheng, Jin Yuli, Ma Pengtao
Yantai Key Laboratory of Characteristic Agricultural Biological Resources Conservation and Germplasm Innovative Utilization, College of Life Sciences, Yantai University, Yantai 264005, China.
School of Life Sciences, Henan University, Kaifeng 475004, China.
Int J Mol Sci. 2024 Dec 30;26(1):242. doi: 10.3390/ijms26010242.
Powdery mildew, caused by f. sp. (), is a disease that seriously harms wheat production and occurs in all wheat-producing areas around the world. Exploring gene(s) and developing resistant cultivars are preferred to control the disease. Wild emmer wheat (, 2n = 4x = 28, AABB) has accumulated abundant gene resources for resistance to powdery mildew during the long process of natural evolution. In the current study, the WEW accession D430 was highly resistant to powdery mildew at the whole-growth stage. Genetic analysis showed that the powdery mildew resistance in D430 was conferred by a single dominant locus or gene by the cross of D430 and susceptible durum wheat 647, tentatively named . Combining BSR-Seq analysis, molecular mapping, and sequence alignment, was finally mapped to locus, and the sequence was identical to . Subsequently, 1871 DEGs between resistant and susceptible bulks were annotated and analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment. Eight disease-related genes were evaluated by qRT-PCR and exhibited a unique expression pattern when invaded by isolate E09 and was, therefore, presented as latent targets for regulating powdery mildew resistance in D430.
白粉病由小麦白粉菌(Blumeria graminis f. sp. tritici)引起,是一种严重危害小麦生产的病害,在世界所有小麦产区均有发生。探索抗病基因并培育抗病品种是防治该病害的首选方法。野生二粒小麦(Triticum dicoccoides,2n = 4x = 28,AABB)在长期自然进化过程中积累了丰富的抗白粉病基因资源。在本研究中,野生二粒小麦材料D430在整个生育期对白粉病具有高度抗性。遗传分析表明,通过D430与感病硬粒小麦647杂交,D430对白粉病的抗性由一个单显性位点或基因控制,暂命名为PmD430。结合BSR-Seq分析、分子定位和序列比对,最终将PmD430定位到5BL位点,其序列与Pm5e相同。随后,对抗感混合池之间的1871个差异表达基因(DEGs)进行了注释,并通过基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析。通过qRT-PCR对8个与病害相关的基因进行了评估,这些基因在受到白粉菌E09分离株侵染时表现出独特的表达模式,因此被作为调控D430对白粉病抗性的潜在靶点。