a Department of Plant Physiology, Center for Plant Molecular Biology (ZMBP), University of Tübingen, Auf der Morgenstelle 32, 72076 Tübingen, Germany b Present address: Department of Biology, Norwegian University of Science and Technology (NTNU), Høgskoleringen 5, 7491- Trondheim, Norway.
a Department of Plant Physiology, Center for Plant Molecular Biology (ZMBP), University of Tübingen, Auf der Morgenstelle 32, 72076 Tübingen, Germany.
Mol Plant. 2014 Oct;7(10):1560-77. doi: 10.1093/mp/ssu074. Epub 2014 Jun 19.
As the first and rate-limiting enzyme of proline degradation, PROLINE DEHYDROGENASE1 (PDH1) is tightly regulated during plant stress responses, including induction under hypoosmolarity and repression under water deficit. The plant receptor histidine kinases AHKs, elements of the two-component system (TCS) in Arabidopsis thaliana, are proposed to function in water stress responses by regulating different stress-responsive genes. However, little information is available concerning AHK phosphorelay-mediated downstream signaling. Here we show that the Arabidopsis type-B response regulator 18 (ARR18) functions as a positive osmotic stress response regulator in Arabidopsis seeds and affects the activity of the PDH1 promoter, known to be controlled by C-group bZIP transcription factors. Moreover, direct physical interaction of ARR18 with bZIP63 was identified and shown to be dependent on phosphorylation of the conserved aspartate residue in the ARR18 receiver domain. We further show that bZIP63 itself functions as a negative regulator of seed germination upon osmotic stress. Using reporter gene assays in protoplasts, we demonstrated that ARR18 interaction negatively interferes with the transcriptional activity of bZIP63 on the PDH1 promoter. Our findings provide new insight into the function of ARR18 and bZIP63 as antagonistic regulators of gene expression in Arabidopsis.
作为脯氨酸降解的第一限速酶,脯氨酸脱氢酶 1(PDH1)在植物应激反应中受到严格调控,包括在低渗胁迫下诱导和在水分亏缺下抑制。拟南芥中的植物受体组氨酸激酶 AHKs 是双组分系统(TCS)的组成部分,被认为通过调节不同的应激响应基因在水分胁迫响应中发挥作用。然而,关于 AHK 磷酸传递介导的下游信号传递的信息很少。在这里,我们表明拟南芥 B 型反应调节因子 18(ARR18)在拟南芥种子中作为正向渗透胁迫响应调节剂发挥作用,并影响 PDH1 启动子的活性,已知该启动子受 C 组 bZIP 转录因子控制。此外,鉴定并显示 ARR18 与 bZIP63 之间的直接物理相互作用依赖于 ARR18 接收结构域中保守天冬氨酸残基的磷酸化。我们进一步表明,bZIP63 本身在渗透胁迫下作为种子萌发的负调节剂发挥作用。通过原生质体中的报告基因测定,我们证明 ARR18 相互作用负干扰 bZIP63 在 PDH1 启动子上的转录活性。我们的研究结果为 ARR18 和 bZIP63 作为拟南芥中基因表达的拮抗调节剂的功能提供了新的见解。