Wang Tianjiao, Zheng Kaifeng, Min Qinyue, Li Yihao, Xue Xiuhua, Li Wanjie, Han Shengcheng
Beijing Key Laboratory of Gene Resources and Molecular Development, College of Life Sciences, Beijing Normal University, Beijing 100875, China.
College of Life Sciences, Qinghai Normal University, Xining 810008, China.
Int J Mol Sci. 2025 Aug 28;26(17):8331. doi: 10.3390/ijms26178331.
Mitogen-activated protein kinases 3 and 6 (MPK3/MPK6) are central to pattern-triggered immunity (PTI) and effector-triggered immunity (ETI) in Arabidopsis, yet the involvement of long noncoding RNAs (lncRNAs, >200 nt) in these pathways is poorly understood. Here, transcriptomic analyses were performed to compare lncRNA and protein-coding gene (PCG) expression profiles in wild-type (WT) and MPK3/MPK6-deficient () Arabidopsis plants. These plants were inoculated with either pv. () DC3000, which elicits both PTI and ETI, or its type III secretion-deficient mutant, DC3000 , which induces only PTI. RNA sequencing (RNA-seq) analysis of 18 samples identified 1388 known and 70 novel lncRNAs, among which differentially expressed lncRNAs (DElncRNAs) involved in disease resistance were further identified. Using integrative analyses, including weighted gene co-expression network analysis (WGCNA), prediction of lncRNA -regulatory targets for PCGs, and validation via reverse transcription-quantitative PCR (RT-qPCR), three core lncRNA-mediated regulatory modules were identified: (i) MPK3/MPK6-dependent PTI and ETI, where lncRNAs amplify signals; (ii) MPK3/MPK6-dependent PTI, where lncRNAs fine-tune basal immunity; and (iii) MPK3/MPK6-independent PTI and ETI, where lncRNAs serve as a backup regulatory network. These modules form a multi-layered immune regulatory network via - and -regulation and further enable the identification of lncRNA-PCG pairs involved in both regulatory modes. This work enhances the understanding of the molecular mechanisms underlying plant innate immunity.
丝裂原活化蛋白激酶3和6(MPK3/MPK6)在拟南芥的模式触发免疫(PTI)和效应子触发免疫(ETI)中起核心作用,然而,长链非编码RNA(lncRNA,>200 nt)在这些途径中的作用尚不清楚。在这里,进行了转录组分析,以比较野生型(WT)和MPK3/MPK6缺陷型()拟南芥植物中lncRNA和蛋白质编码基因(PCG)的表达谱。这些植物接种了能引发PTI和ETI的丁香假单胞菌番茄致病变种()DC3000,或其III型分泌缺陷型突变体DC3000,后者仅诱导PTI。对18个样本的RNA测序(RNA-seq)分析鉴定出1388个已知lncRNA和70个新的lncRNA,其中进一步鉴定出参与抗病性的差异表达lncRNA(DElncRNA)。通过综合分析,包括加权基因共表达网络分析(WGCNA)、预测PCG的lncRNA调控靶点以及通过逆转录定量PCR(RT-qPCR)进行验证,确定了三个核心lncRNA介导的调控模块:(i)MPK3/MPK6依赖性PTI和ETI,其中lncRNA放大信号;(ii)MPK3/MPK6依赖性PTI,其中lncRNA微调基础免疫;(iii)MPK3/MPK6非依赖性PTI和ETI,其中lncRNA作为备用调控网络。这些模块通过正向和负向调控形成多层免疫调控网络,并进一步能够鉴定参与两种调控模式的lncRNA-PCG对。这项工作增进了对植物先天免疫分子机制的理解。