He Siou-Luan, Li Bin, Zahurancik Walter J, Arthur Henry C, Sidharthan Vaishnavi, Gopalan Venkat, Wang Lei, Jang Jyan-Chyun
Department of Horticulture and Crop Science, The Ohio State University, Columbus, OH, United States.
Center for Applied Plant Sciences, The Ohio State University, Columbus, OH, United States.
Front Plant Sci. 2024 May 8;15:1375478. doi: 10.3389/fpls.2024.1375478. eCollection 2024.
Tandem CCCH zinc finger (TZF) proteins play diverse roles in plant growth and stress response. Although as many as 11 TZF proteins have been identified in , little is known about the mechanism by which TZF proteins select and regulate the target mRNAs. Here, we report that TZF1 is a bona-fide stress granule protein. Ectopic expression of (), but not an mRNA binding-defective mutant (), enhances salt stress tolerance in . RNA-seq analyses of NaCl-treated plants revealed that the down-regulated genes in plants are enriched for functions in salt and oxidative stress responses. Because many of these down-regulated mRNAs contain AU- and/or U-rich elements (AREs and/or UREs) in their 3'-UTRs, we hypothesized that TZF1-ARE/URE interaction might contribute to the observed gene expression changes. Results from RNA immunoprecipitation-quantitative PCR analysis, gel-shift, and mRNA half-life assays indicate that TZF1 binds and triggers degradation of the () mRNA, which encodes a tonoplast-localized calcium pump that extrudes calcium and dampens signal transduction pathways necessary for salt stress tolerance. Furthermore, this salt stress-tolerance phenotype was recapitulated in null mutants. Collectively, our findings demonstrate that TZF1 binds and initiates degradation of specific mRNAs to enhance salt stress tolerance.
串联CCCH锌指(TZF)蛋白在植物生长和应激反应中发挥多种作用。尽管在[具体植物名称未给出]中已鉴定出多达11种TZF蛋白,但对于TZF蛋白选择和调控靶mRNA的机制知之甚少。在此,我们报道TZF1是一种真正的应激颗粒蛋白。[具体基因名称未给出]的异位表达(而非mRNA结合缺陷突变体)增强了[具体植物名称未给出]对盐胁迫的耐受性。对NaCl处理植物的RNA测序分析表明,[具体植物名称未给出]植物中下调的基因在盐和氧化应激反应功能方面富集。由于许多这些下调的mRNA在其3'非翻译区含有富含AU和/或U的元件(AREs和/或UREs),我们推测TZF1与ARE/URE的相互作用可能导致了观察到的基因表达变化。RNA免疫沉淀定量PCR分析、凝胶迁移和mRNA半衰期测定结果表明,TZF1结合并触发编码液泡膜定位钙泵的[具体基因名称未给出]mRNA的降解,该钙泵可排出钙并抑制盐胁迫耐受性所需的信号转导途径。此外,在[具体植物名称未给出]基因敲除突变体中重现了这种盐胁迫耐受性表型。总体而言,我们的研究结果表明,TZF1结合并启动特定mRNA的降解以增强盐胁迫耐受性。