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首页> 外文期刊>The Plant Cell >The WRKY6 Transcription Factor Modulates PHOSPHATE1 Expression in Response to Low Pi Stress in Arabidopsis.
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The WRKY6 Transcription Factor Modulates PHOSPHATE1 Expression in Response to Low Pi Stress in Arabidopsis.

机译:WRKY6转录因子调节拟南芥中低磷胁迫下的PHOSPHATE1表达。

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摘要

Arabidopsis thaliana WRKY family comprises 74 members and some of them are involved in plant responses to biotic and abiotic stresses. This study demonstrated that WRKY6 is involved in Arabidopsis responses to low-Pi stress through regulating PHOSPHATE1 (PHO1) expression. WRKY6 overexpression lines, similar to the pho1 mutant, were more sensitive to low Pi stress and had lower Pi contents in shoots compared with wild-type seedlings and the wrky6-1 mutant. Immunoprecipitation assays demonstrated that WRKY6 can bind to two W-boxes of the PHO1 promoter. RNA gel blot and beta-glucuronidase activity assays showed that PHO1 expression was repressed in WRKY6-overexpressing lines and enhanced in the wrky6-1 mutant. Low Pi treatment reduced WRKY6 binding to the PHO1 promoter, which indicates that PHO1 regulation by WRKY6 is Pi dependent and that low Pi treatment may release inhibition of PHO1 expression. Protein gel blot analysis showed that the decrease in WRKY6 protein induced by low Pi treatment was inhibited by a 26S proteosome inhibitor, MG132, suggesting that low Pi-induced release of PHO1 repression may result from 26S proteosome-mediated proteolysis. In addition, WRKY42 also showed binding to W-boxes of the PHO1 promoter and repressed PHO1 expression. Our results demonstrate that WRKY6 and WRKY42 are involved in Arabidopsis responses to low Pi stress by regulation of PHO1 expression.
机译:拟南芥WRKY家族由74个成员组成,其中一些成员参与植物对生物和非生物胁迫的反应。这项研究表明WRKY6通过调节PHOSPHATE1(PHO1)表达参与拟南芥对低Pi胁迫的反应。与野生型幼苗和wrky6-1突变体相比,与pho1突变体相似的WRKY6过表达株系对低Pi胁迫更为敏感,并且芽中的Pi含量较低。免疫沉淀分析表明WRKY6可以结合PHO1启动子的两个W-box。 RNA凝胶印迹和β-葡萄糖醛酸苷酶活性测定表明,PHO1表达在WRKY6过表达株中受到抑制,而在wrky6-1突变株中得到增强。低磷处理降低了WRKY6与PHO1启动子的结合,这表明WRKY6对PHO1的调控是Pi依赖性的,低磷处理可能会释放PHO1表达的抑制作用。蛋白凝胶印迹分析表明,低Pi处理诱导的WRKY6蛋白的减少受到26S蛋白体抑制剂MG132的抑制,这表明低Pi诱导的PHO1抑制的释放可能是由26S蛋白体介导的蛋白水解作用引起的。此外,WRKY42还显示与PHO1启动子的W-box结合并抑制PHO1表达。我们的结果表明,WRKY6和WRKY42通过调节PHO1表达参与拟南芥对低Pi胁迫的反应。

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