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Oscillating Aquaporin Phosphorylation and 14-3-3 Proteins Mediate the Circadian Regulation of Leaf Hydraulics

机译:振荡的水通道蛋白磷酸化和14-3-3蛋白质介导叶水力学的昼夜调节。

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摘要

The circadian clock regulates plant tissue hydraulics to synchronize water supply with environmental cycles and thereby optimize growth. The circadian fluctuations in aquaporin transcript abundance suggest that aquaporin water channels play a role in these processes. Here, we show that hydraulic conductivity (Kros) of Arabidopsis (Arabidopsis thaliana) rosettes displays a genuine circadian rhythmicity with a peak around midday. Combined immunological and proteomic approaches revealed that phosphorylation at two C-terminal sites (Ser280, Ser283) of PLASMA MEMBRANE INTRINSIC PROTEIN 2;1 (AtPIP2;1), a major plasma membrane aquaporin in rosettes, shows circadian oscillations and is correlated with Kros. Transgenic expression of phosphodeficient and phosphomimetic forms of this aquaporin indicated that AtPIP2;1 phosphorylation is necessary but not sufficient for Kros regulation. We investigated the supporting role of 14-3-3 proteins, which are known to interact with and regulate phosphorylated proteins. Individual knockout plants for five 14-3-3 protein isoforms expressed in rosettes lacked circadian activation of Kros. Two of these [GRF4 (14-3-3Phi); GRF10 (14-3-3Epsilon)] showed direct interactions with AtPIP2;1 in the plant and upon coexpression in Xenopus laevis oocytes and activated AtPIP2;1, preferentially when the latter was phosphorylated at its two C-terminal sites. We propose that this regulatory mechanism assists in the activation of phosphorylated AtPIP2;1 during circadian regulation of Kros.
机译:该生物钟调节植物组织的水力学,以使供水与环境循环同步,从而优化生长。水通道蛋白转录本丰度的昼夜节律波动表明水通道蛋白水通道在这些过程中起作用。在这里,我们显示拟南芥(Arabidopsis thaliana)莲座丛的水力传导率(Kros)显示出真正的昼夜节律,并在午间左右达到峰值。结合的免疫学和蛋白质组学方法表明,玫瑰花结膜中主要的质膜水通道蛋白PLASMA膜内在蛋白2; 1(AtPIP2; 1)的两个C末端位点(Ser280,Ser283)磷酸化,显示出昼夜节律振荡并与Kros相关。该水通道蛋白的磷酸缺陷型和磷酸化形式的转基因表达表明,AtPIP2; 1磷酸化是必需的,但不足以进行Kros调节。我们研究了14-3-3蛋白的支持作用,这些蛋白与磷酸化蛋白相互作用并调节它们。在花环中表达的五个14-3-3蛋白质同工型的单独敲除植物缺乏Kros的昼夜节律激活。其中两个[GRF4(14-3-3Phi); GRF10(14-3-3Epsilon)]在植物中以及在非洲爪蟾卵母细胞中共表达后与AtPIP2; 1直接相互作用,并激活了AtPIP2; 1,优先当后者在其两个C末端位点被磷酸化时。我们建议这种调节机制有助于在Kros的昼夜调节过程中磷酸化AtPIP2; 1的激活。

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