1长江大学农学院,湖北荆州433200;2中国农业科学院作物科学研究所,北京 100081;3凉山彝族自治州农业科学研究院高寒农业研究所, 四川凉山 615000;4昭通市农业科学院,云南昭通 657000
研究方向为作物遗传育种,E-mail: 2275620061@qq.com
方正武,研究方向为麦类资源创新与利用,E-mail: fangzhengwu88@163.com
周美亮,研究方向为作物种质资源及遗传育种学,E-mail: zhoumeiliang@caas.cn
国家自然科学基金(32161143005);云南省科技人才与平台计划(202505AF350051);昭通市院士专家工作站项目(2024ZTYX06);凉山州农业科技“揭榜挂帅”项目(LSNY2024003)
1College of Agriculture, Yangtze University, Jingzhou 433200, Hubei;2Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081;3Alpine Agriculture Research Institute,Academy of Agricultural Sciences · Liangshan, Liangshan 615000, Sichuan;4Zhaotong City Academy of Agricultural Sciences, Zhaotong 657000, Yunnan
National Natural Science Foundation of China (32161143005); Yunnan Provincial Science and Technology Talent and Platform Program (202505AF350051); Zhaotong City Academician and Expert Workstation Project (2024ZTYX06); Liangshan Prefecture Agricultural Science and Technology "Unveiling and Assuming Leadership" Project (LSNY2024003)
立枯丝核菌(Rhizoctonia solani)引起的立枯病严重威胁苦荞[Fagopyrum tataricum(L.)Gaertn.]生产。本团队前期研究发现,多聚半乳糖醛酸酶(PG)家族基因FtADPG2可能与苦荞立枯病抗性相关,为深入了解该基因在立枯病抗性中发挥的作用,以中苦3号为材料,克隆获得FtADPG2,其编码一个41.65 kDa稳定蛋白。表达分析显示,该基因表达受立枯丝核菌侵染显著诱导,并与病程相关蛋白PR1表达及茉莉酸积累趋势一致。过表达FtADPG2显著增强烟草和拟南芥的感病性。单倍型分析发现该基因的第一外显子存在Ala22Val变异(Hap2),Hap2表现出更高酶活性和更强感病性。基于转录组与AlphaFold预测筛选到毒力蛋白RsEgD,通过酵母双杂交与荧光素酶互补实验证实其与FtADPG2互作。结果表明,FtADPG2是调控苦荞感病性的关键基因,其通过与病原菌毒力蛋白RsEgD互作协同促进侵染。本研究为阐明苦荞-立枯丝核菌互作机制及荞麦抗病育种提供了新靶点与理论依据。
Sheath blight caused by Rhizoctonia solani poses a serious threat to the production of tartary buckwheat (Fagopyrum tataricum). Previous work by our group suggested that FtADPG2, a gene from the polygalacturonase (PG) family, might be associated with sheath blight resistance in tartary buckwheat. To gain deeper insights into the functional role of this gene in disease resistance, we cloned FtADPG2 from the cultivar Zhongku 3. The gene encodes a stable protein with a molecular weight of 41.65 kDa. Expression analysis revealed that FtADPG2 transcription was significantly induced upon R. solani infection, and this induction showed a coordinated upregulation with the expression of the pathogenesis-related protein PR1 and the accumulation of jasmonic acid. Heterologous overexpression of FtADPG2 significantly enhanced disease susceptibility in both tobacco and Arabidopsis. Haplotype analysis identified a natural variation (Ala22Val) within the first exon, defining a haplotype designated Hap2. Notably, Hap2 was associated with higher enzymatic activity and conferred a greater susceptibility phenotype. Based on transcriptomic data and AlphaFold structure prediction, we identified a candidate fungal virulence protein, RsEgD. Protein-protein interaction between FtADPG2 and RsEgD was subsequently confirmed by yeast two-hybrid and luciferase complementation imaging assays. Our results demonstrate that FtADPG2 is a key susceptibility gene in tartary buckwheat, promoting infection through a physical interaction with the pathogen effector RsEgD. This study provides crucial targets and a theoretical foundation for elucidating the molecular mechanisms of F.tataricum-R.solani interaction and for breeding buckwheat varieties with enhanced disease resistance.
范红萍,樊冬晴,朱剑锋,等.苦荞
