Su Chang, Li Xue, Dong Ye, Daniel Bimpong, Liu Chao, Xing Yujun, Ma Dongfang
Ministry of Agriculture and Rural Affairs (MARA) Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co-Construction by Ministry and Province), College of Agriculture, Yangtze University, Jingzhou, 434025, China.
Ministry of Agriculture and Rural Affairs (MARA) Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co-Construction by Ministry and Province), College of Agriculture, Yangtze University, Jingzhou, 434025, China; Jiangsu Key Laboratory for Food Quality and Safety, Institute of Food Safety and Nutrition, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Plant Physiol Biochem. 2025 Jul;224:109898. doi: 10.1016/j.plaphy.2025.109898. Epub 2025 Apr 9.
Intergenic long non-coding RNAs (lincRNAs) have recently been recognized as pivotal regulators in plant-pathogen interactions. However, the specific regulatory mechanisms of lincRNAs responding to Fusarium graminearum (F. graminearum) infection remain largely unexplored. Here, we performed time-series transcriptome profiling (0, 24, 48, and 72 h post-inoculation) and systematic identification of lincRNAs. A total of 1238 expressed lincRNAs were identified, among which 548 were differentially expressed lincRNAs during the time course of F. graminearum infection. We further predicted cis-regulatory lincRNA-mRNA pairs, comprising 347 lincRNAs and potential 1015 target genes, which were found to be mainly involved in amino acid metabolism and biosynthetic pathways. Moreover, 19 lincRNAs were predicted as putative precursors or endogenous target mimics of miRNAs. Subsequently, we verified that two lincRNAs, MSTRG.6494 and MSTRG.32080, showed strong transcriptional responses to F. graminearum infection by quantitative real-time PCR (qPCR) screening. Silencing MSTRG.6494 reduced the expression level of defense-related genes, resulting in reduced resistance to fungal pathogenicity. Meanwhile, the expression level of the potential target gene ATP synthase subunit beta (TaATP2) was significantly decreased in MSTRG.6494-silenced plants infected with F. graminearum. Overall, we performed the genome-wide identification of lincRNAs and their possible regulatory networks during F. graminearum infection-related process, confirming that MSTRG.6494 participates in wheat resistance to F. graminearum, may be via targeting TaATP2 to enhance defense responses. Our findings provide new insights into the regulatory mechanism of lincRNAs for Fusarium head blight (FHB) resistance, suggesting this mechanism as an essential strategy for protecting wheat from F. graminearum.
基因间长链非编码RNA(lincRNA)最近被认为是植物与病原体相互作用中的关键调节因子。然而,lincRNA响应禾谷镰刀菌(F. graminearum)感染的具体调控机制仍 largely未被探索。在此,我们进行了时间序列转录组分析(接种后0、24、48和72小时)并对lincRNA进行了系统鉴定。共鉴定出1238个表达的lincRNA,其中548个是在禾谷镰刀菌感染过程中差异表达的lincRNA。我们进一步预测了顺式调控的lincRNA - mRNA对,包括347个lincRNA和潜在的1015个靶基因,发现它们主要参与氨基酸代谢和生物合成途径。此外,19个lincRNA被预测为miRNA的假定前体或内源性靶标模拟物。随后,我们通过定量实时PCR(qPCR)筛选验证了两个lincRNA,MSTRG.6494和MSTRG.32080,对禾谷镰刀菌感染表现出强烈的转录反应。沉默MSTRG.6494降低了防御相关基因的表达水平,导致对真菌致病性的抗性降低。同时,在感染禾谷镰刀菌的MSTRG.6494沉默植株中,潜在靶基因ATP合酶β亚基(TaATP2)的表达水平显著降低。总体而言,我们在禾谷镰刀菌感染相关过程中进行了lincRNA及其可能调控网络的全基因组鉴定,证实MSTRG.6494参与小麦对禾谷镰刀菌的抗性,可能是通过靶向TaATP2来增强防御反应。我们的发现为lincRNA在赤霉病(FHB)抗性中的调控机制提供了新见解,表明该机制是保护小麦免受禾谷镰刀菌侵害的重要策略。