Jia Pei, Tang Ye, Hu Guang, Quan Yonggang, Chen Aimin, Zhong Naiqin, Peng Qingzhong, Wu Jiahe
Hunan Provincial Key Laboratory of Plant Resources Conservation and Utilization, College of Biology and Environmental Sciences, Jishou University, Jishou, China.
State Key Laboratory of Plant Genomics, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Front Plant Sci. 2022 May 20;13:870882. doi: 10.3389/fpls.2022.870882. eCollection 2022.
Teosinte branched1/Cincinnata/proliferating cell factor (TCP) transcription factors play important roles in plant growth and defense. However, the molecular mechanisms of TCPs participating in plant defense remain unclear. Here, we characterized a cotton TCP4-like fine-tuned by miR319b, which could interact with NON-EXPRESSER OF PATHOGEN-RELATED GENES 1 (NPR1) to directly activate () expression, facilitating plant resistance against . mRNA degradome data and GUS-fused assay showed that mRNA was directedly cleaved by ghr-miR319b. Knockdown of ghr-miR319b increased plant resistance to , whereas silencing increased plant susceptibility by the virus-induced gene silencing (VIGS) method, suggesting that is a positive regulator of plant defense. According to the electrophoretic mobility shift assay and GUS reporter analysis, GhTCP4-like could transcriptionally activate expression, resulting in increased salicylic acid (SA) accumulation. Yeast two-hybrid and luciferase complementation image analyses demonstrated that interacts with , which can promote transcriptional activation in expression according to the GUS reporter assay. Together, these results revealed that GhTCP4-like interacts with GhNPR1 to promote expression through fine-tuning of ghr-miR319b, leading to SA accumulation, which is percepted by NPR1 to increase plant defense against . Therefore, GhTCP4-like participates in a positive feedback regulation loop of SA biosynthesis via NPR1, increasing plant defenses against fungal infection.
玉米分枝1/辛辛那提/增殖细胞因子(TCP)转录因子在植物生长和防御中发挥重要作用。然而,TCP参与植物防御的分子机制仍不清楚。在此,我们鉴定了一个受miR319b微调的棉花类TCP4,它可以与病程相关基因非表达子1(NPR1)相互作用,直接激活()的表达,促进植物对()的抗性。mRNA降解组数据和GUS融合分析表明,()mRNA被ghr-miR319b直接切割。通过病毒诱导基因沉默(VIGS)方法敲低ghr-miR319b可增强植物对()的抗性,而沉默()则增加植物的易感性,这表明()是植物防御的正调控因子。根据电泳迁移率变动分析和GUS报告基因分析,类GhTCP4可以转录激活()的表达,导致水杨酸(SA)积累增加。酵母双杂交和荧光素酶互补成像分析表明,()与()相互作用,根据GUS报告基因分析,()可以促进()在()表达中的转录激活。总之,这些结果表明,类GhTCP4与GhNPR1相互作用,通过微调ghr-miR319b促进()表达,导致SA积累,NPR1感知到SA积累从而增强植物对()的防御。因此,类GhTCP4通过NPR1参与SA生物合成的正反馈调节环,增强植物对真菌感染的防御。