Bowen Zhou, Linjing Wang, Zhenyang Ji, Xiaoman Chen, Xingkai Sun, Na Xu, Peng Li, Ya Lin Sang, Qingzhang Du, Li-Jun Liu
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引用次数: 0
Abstract
Salt stress is a major abiotic stress restrict plant growth and distribution. In our previous study, we found the ABI5-BINDING PROTEIN 2a (PagAFP2a) gene was rapidly and significantly induced by salt stress in hybrid poplar (Populus alba × Populus glandulosa), however, its function in salt stress responses was unclear. In this study, we further demonstrated that the PagAFP2a gene expression is significantly induced by salt and ABA treatments. Additionally, the ABA-responsive element (ABRE) binding proteins (PagAREB1s) directly bind to PagAFP2a promoter and activate its expression. Physiological analysis showed that PagAFP2a overexpression (PagAFP2aOE) or PagAREB1-3 knockout (PagAREB1-3KO) significantly reduced salt tolerance whereas PagAFP2a knockout (PagAFP2aKO) or PagAREB1-3 overexpression (PagAREB1-3OE) significantly enhanced salt tolerance in poplar. Correspondingly, salt stress responsive genes were significantly upregulated in PagAFP2aKO and PagAREB1-3OE plants while downregulated in PagAFP2aOE and PagAREB1-3KO plants. Furthermore, we demonstrated that PagAFP2a directly interacts with PagAREB1s and represses its transcriptional activity at the target genes. In summary, our results unveil the PagAFP2a-PagAREB1s module form a negative feedback loop in ABA signaling to fine-tune salt stress responses in Populus.
盐胁迫是制约植物生长和分布的主要非生物胁迫。在我们之前的研究中,我们发现杂交白杨(Populus alba × Populus glandulosa)的ABI5-BINDING PROTEIN 2a (PagAFP2a)基因在盐胁迫下被快速显著诱导,但其在盐胁迫应答中的功能尚不清楚。在本研究中,我们进一步证明了盐和ABA处理显著诱导PagAFP2a基因的表达。此外,aba响应元件(ABRE)结合蛋白(pagareb1)直接结合PagAFP2a启动子并激活其表达。生理分析显示,PagAFP2a过表达(PagAFP2aOE)或PagAREB1-3敲除(PagAREB1-3KO)显著降低了杨树的耐盐性,而PagAFP2a敲除(PagAFP2aKO)或PagAREB1-3过表达(PagAREB1-3OE)显著增强了杨树的耐盐性。相应的,盐胁迫响应基因在PagAFP2aKO和PagAREB1-3OE植物中显著上调,而在PagAFP2aOE和PagAREB1-3KO植物中显著下调。此外,我们证明PagAFP2a直接与pagareb1相互作用,并抑制其在靶基因上的转录活性。综上所述,我们的研究结果揭示了PagAFP2a-PagAREB1s模块在ABA信号中形成负反馈回路,以微调杨树的盐胁迫反应。
期刊介绍:
Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.