College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, China.
School of Agriculture, Policy and Development, University of Reading, Reading, RG6 6AR, UK.
Plant J. 2022 Sep;111(6):1753-1767. doi: 10.1111/tpj.15922. Epub 2022 Aug 6.
Phosphorus (P) is an important nutrient for plants. Here, we identify a WRKY transcription factor (TF) in poplar (Populus deltoides × Populus euramericana) (PdeWRKY65) that modulates tissue phosphate (Pi) concentrations in poplar. PdeWRKY65 overexpression (OE) transgenic lines showed reduced shoot Pi concentrations under both low and normal Pi availabilities, while PdeWRKY65 reduced expression (RE) lines showed the opposite phenotype. A gene encoding a Pi transporter (PHT), PdePHT1;9, was identified as the direct downstream target of PdeWRKY65 by RNA sequencing (RNA-Seq). The negative regulation of PdePHT1;9 expression by PdeWRKY65 was confirmed by DNA-protein interaction assays, including yeast one-hybrid (Y1H), electrophoretic mobility shift assay (EMSA), co-expression of the promoters of PdePHT1;9 and PdeWRKY65 in tobacco (Nicotiana benthamiana) leaves, and chromatin immunoprecipitation-quantitative PCR. A second WRKY TF, PdeWRKY6, was subsequently identified and confirmed to positively regulate the expression of PdePHT1;9 by DNA-protein interaction assays. PdePHT1;9 and PdeWRKY6 OE and RE poplar transgenic lines were used to confirm their positive regulation of shoot Pi concentrations, under both normal and low Pi availabilities. No interaction between PdeWRKY6 and PdeWRKY65 was observed at the DNA or protein levels. Collectively, these data suggest that the low Pi-responsive TFs PdeWRKY6 and PdeWRKY65 independently regulate the expression of PHT1;9 to modulate tissue Pi concentrations in poplar.
磷(P)是植物的重要营养物质。在这里,我们鉴定了杨树(Populus deltoides×Populus euramericana)(PdeWRKY65)中的一个 WRKY 转录因子(TF),该 TF 调节杨树中的组织磷(Pi)浓度。PdeWRKY65 过表达(OE)转基因株系在低磷和正常磷供应下表现出降低的地上部 Pi 浓度,而 PdeWRKY65 表达降低(RE)株系表现出相反的表型。通过 RNA 测序(RNA-Seq)鉴定了一个编码 Pi 转运蛋白(PHT)的基因,PdePHT1;9,是 PdeWRKY65 的直接下游靶标。通过 DNA-蛋白互作实验,包括酵母单杂交(Y1H)、电泳迁移率变动分析(EMSA)、在烟草(Nicotiana benthamiana)叶片中共表达 PdePHT1;9 和 PdeWRKY65 的启动子,以及染色质免疫沉淀定量 PCR,证实了 PdeWRKY65 对 PdePHT1;9 表达的负调控。随后鉴定并证实了第二个 WRKY TF,PdeWRKY6,通过 DNA-蛋白互作实验正向调控 PdePHT1;9 的表达。PdePHT1;9 和 PdeWRKY6 OE 和 RE 杨树转基因株系用于在正常和低 Pi 供应下确认它们对地上部 Pi 浓度的正向调控。在 DNA 或蛋白水平均未观察到 PdeWRKY6 和 PdeWRKY65 之间的相互作用。综上所述,这些数据表明低 Pi 响应 TF PdeWRKY6 和 PdeWRKY65 独立调节 PHT1;9 的表达,以调节杨树中的组织 Pi 浓度。