Fan Gaofeng, Gao Yuan, Wu Xinyue, Yu Yingying, Yao Wenjing, Jiang Jiahui, Liu Huanzhen, Jiang Tingbo
State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Co-Innovation Center for Sustainable Forestry in Southern China/Bamboo Research Institute, Nanjing Forestry University, Nanjing, China.
Plant Genome. 2024 Dec;17(4):e20521. doi: 10.1002/tpg2.20521. Epub 2024 Oct 16.
Poplar trees are crucial for timber and greening, but high levels of salt in the soil have severely limited the yield of poplar. Ethylene response factor (ERF) transcription factors play an important role in growth, development, and stress response in eukaryotes. Our study focused on the PagERF021 gene from Populus alba × P. glandulosa, which was significantly upregulated in various tissues under salt stress [Correction added on October 4, 2024, after first online publication: "ETS2 reporter factor" is changed to "Ethylene response factor".]. Both the tissue-specific expression pattern and β-glucuronidase (GUS) staining of proPagERF021-GUS plants indicated that this gene was predominantly expressed in the roots and stems. The subcellular localization showed that the protein was only localized in the nucleus. The yeast assay demonstrated that this protein had transcriptional activation activity at its C-terminal and could specifically binding to the MYB-core cis-element. The overexpression of PagERF021 gene could scavenge the accumulation of reactive oxygen species and reduce the degree of cellular membrane damage, indicating that this gene enhanced the salt tolerance of poplars. This finding will provide a feasible insight for future research into the regulatory mechanisms of ERF genes in resisting to abiotic stress and the development of new stress-resistant varieties in plants.
杨树对于木材和绿化至关重要,但土壤中的高盐分严重限制了杨树的产量。乙烯响应因子(ERF)转录因子在真核生物的生长、发育和应激反应中发挥着重要作用。我们的研究聚焦于来自银白杨×腺毛杨的PagERF021基因,该基因在盐胁迫下的各种组织中显著上调[2024年10月4日首次在线发表后添加的更正:“ETS2报告因子”改为“乙烯响应因子”]。proPagERF021-GUS植株的组织特异性表达模式和β-葡萄糖醛酸酶(GUS)染色均表明该基因主要在根和茎中表达。亚细胞定位显示该蛋白仅定位于细胞核。酵母实验表明该蛋白在其C端具有转录激活活性,并能特异性结合MYB核心顺式元件。PagERF021基因的过表达可以清除活性氧的积累并降低细胞膜损伤程度,表明该基因增强了杨树的耐盐性。这一发现将为未来研究ERF基因在抵抗非生物胁迫中的调控机制以及植物新抗逆品种的培育提供可行的思路。