College of Life Science, Key Laboratory for Bio-Resources and Eco-Environment of Ministry of Education, Sichuan University, Chengdu, 610065, China.
College of Life Sciences, Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, 610065, China.
Plant Physiol. 2022 Nov 28;190(4):2688-2705. doi: 10.1093/plphys/kiac404.
Plants usually suffer from phosphorus starvation because of the low inorganic phosphate (Pi) status of most soils. To cope with this, plants have evolved an adaptive phosphate starvation response (PSR) which involves both developmental and metabolic changes regulated mainly by PHOSPHATE STARVATION RESPONSE1 (PHR1) and its homologs. Here, we elucidated how perennial woody plants, such as poplars (Populus spp.), respond to low-Pi stress. We first performed RNA-seq analysis of low-Pi-treated poplars and identified PtoWRKY40 is rapidly downregulated and protein degraded after stress. Overexpressing and knocking-down PtoWRKY40 downregulated and upregulated the expression of Pi starvation signaling genes, respectively, such as PHOSPHATE TRANSPORTER1 (PHT1)-type genes and PURPLE ACID PHOSPHATASE genes. PtoWRKY40 bound to the W box in the promoter of several PtoPHT1s and repressed their expression. Moreover, PtoWRKY40 interacted with PtoPHR1-LIKE3 (PtoPHL3), a PHR1 homolog in poplar, to inhibit the latter binding to the P1BS element and thus reduced PtoPHT1s' transcription under Pi-sufficient conditions. However, Pi deficiency decreased PtoWRKY40 abundance and therefore released its inhibition on PHT1s. In conclusion, we have uncovered a PSR mechanism mediated by PtoWRKY40 and PtoPHL3 which regulates Pi content in poplars, deepening our understanding of how poplars adapt to diverse Pi conditions and regulate appropriate responses to maintain Pi homeostasis.
植物通常会遭受磷饥饿,因为大多数土壤中的无机磷酸盐 (Pi) 含量较低。为了应对这种情况,植物已经进化出适应性的磷饥饿反应(PSR),其中包括由 PHOSPHATE STARVATION RESPONSE1 (PHR1) 和其同源物主要调节的发育和代谢变化。在这里,我们阐明了杨树(Populus spp.)等多年生木本植物如何应对低 Pi 胁迫。我们首先对低 Pi 处理的杨树进行了 RNA-seq 分析,发现 PtoWRKY40 在胁迫后迅速下调并被蛋白降解。过表达和敲低 PtoWRKY40 分别下调和上调了 Pi 饥饿信号基因的表达,如 PHOSPHATE TRANSPORTER1 (PHT1)-type 基因和 PURPLE ACID PHOSPHATASE 基因。PtoWRKY40 结合到几个 PtoPHT1s 启动子中的 W 框上,抑制它们的表达。此外,PtoWRKY40 与杨树中的 PHR1 同源物 PtoPHR1-LIKE3 (PtoPHL3) 相互作用,抑制后者结合到 P1BS 元件上,从而减少了 Pi 充足条件下 PtoPHT1s 的转录。然而,Pi 缺乏会降低 PtoWRKY40 的丰度,从而解除其对 PHT1s 的抑制。总之,我们揭示了由 PtoWRKY40 和 PtoPHL3 介导的 PSR 机制,该机制调节杨树中的 Pi 含量,加深了我们对杨树如何适应不同 Pi 条件并调节适当的反应以维持 Pi 平衡的理解。