Root Biology Center, South China Agricultural University, Guangzhou 510642, China; College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510642, China.
College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510642, China.
J Hazard Mater. 2023 Oct 15;460:132496. doi: 10.1016/j.jhazmat.2023.132496. Epub 2023 Sep 6.
Cadmium (Cd) has long been recognized as toxic pollutant to crops worldwide. The biosynthesis of glutathione-dependent phytochelatin (PC) plays crucial roles in the detoxification of Cd in plants. However, its regulatory mechanism remains elusive. Here, we revealed that Arabidopsis transcription factor WRKY45 confers Cd tolerance via promoting the expression of PC synthesis-related genes PCS1 and PCS2, respectively. Firstly, we found that Cd stress induces the transcript levels of WRKY45 and its protein abundance. Accordingly, in contrast to wild type Col-0, the increased sensitivity to Cd is observed in wrky45 mutant, while overexpressing WRKY45 plants are more tolerant to Cd. Secondly, quantitative real-time PCR revealed that the expression of AtPCS1 and AtPCS2 is stimulated in overexpressing WRKY45 plants, but decreased in wrky45 mutant. Thirdly, WRKY45 promotes the expression of PCS1 and PCS2, electrophoresis mobility shift assay analysis uncovered that WRKY45 directly binds to the W-box cis-element of PCS2 promoter. Lastly, the overexpression of WRKY45 in Col-0 leads to more accumulation of PCs in Arabidopsis, and the overexpression of PCS1 or PCS2 in wrky45 mutant plants rescues the phenotypes induced by Cd stress. In conclusion, our results show that AtWRKY45 positively regulates Cd tolerance in Arabidopsis via activating PCS1 and PCS2 expression.
镉(Cd)长期以来一直被认为是全球作物的有毒污染物。谷胱甘肽依赖的植物螯合肽(PC)的生物合成在植物中 Cd 的解毒中起着至关重要的作用。然而,其调控机制仍不清楚。在这里,我们揭示了拟南芥转录因子 WRKY45 通过分别促进 PC 合成相关基因 PCS1 和 PCS2 的表达来赋予 Cd 耐受性。首先,我们发现 Cd 胁迫诱导 WRKY45 的转录水平及其蛋白丰度增加。因此,与野生型 Col-0 相比,wrky45 突变体对 Cd 的敏感性增加,而 WRKY45 过表达植物对 Cd 更耐受。其次,定量实时 PCR 显示 AtPCS1 和 AtPCS2 的表达在 WRKY45 过表达植物中受到刺激,但在 wrky45 突变体中降低。第三,WRKY45 促进 PCS1 和 PCS2 的表达,电泳迁移率变动分析显示 WRKY45 直接结合 PCS2 启动子的 W-box 顺式元件。最后,WRKY45 在 Col-0 中的过表达导致拟南芥中 PC 的积累增加,而 wrky45 突变体植物中 PCS1 或 PCS2 的过表达挽救了 Cd 胁迫诱导的表型。总之,我们的结果表明 AtWRKY45 通过激活 PCS1 和 PCS2 的表达正向调节拟南芥对 Cd 的耐受性。