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Termination of Shoot Gravitropic Responses by Auxin Feedback on PIN3 Polarity

机译:生长素对PIN3极性的反馈终止芽重力反应。

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摘要

Plants adjust their growth according to gravity. Gravitropism involves gravity perception, signal transduction, and asymmetric growth response, with organ bending as a consequence [1]. Asymmetric growth results from the asymmetric distribution of the plant-specific signaling molecule auxin [2] that is generated by lateral transport, mediated in the hypocotyl predominantly by the auxin transporter PIN-FORMED3 (PIN3) [3-5]. Gravity stimulation polarizes PIN3 to the bottom sides of endodermal cells, correlating with increased auxin accumulation in adjacent tissues at the lower side of the stimulated organ, where auxin induces cell elongation and, hence, organ bending. A curvature response allows the hypocotyl to resume straight growth at a defined angle [6], implying that at some point auxin symmetry is restored to prevent overbending. Here, we present initial insights into cellular and molecular mechanisms that lead to the termination of the tropic response. We identified an auxin feedback on PIN3 polarization as underlying mechanism that restores symmetry of the PIN3-dependent auxin flow. Thus, two mechanistically distinct PIN3 polarization events redirect auxin fluxes at different time points of the gravity response: first, gravity-mediated redirection of PIN3-mediated auxin flow toward the lower hypocotyl side, where auxin gradually accumulates and promotes growth, and later PIN3 polarization to the opposite cell side, depleting this auxin maximum to end the bending. Accordingly, genetic or pharmacological interference with the late PIN3 polarization prevents termination of the response and leads to hypocotyl overbending. This observation reveals a role of auxin feedback on PIN polarity in the termination of the tropic response.
机译:植物根据重力调节其生长。重力作用涉及重力感知,信号转导和不对称生长反应,其结果是器官弯曲[1]。不对称生长是由植物特异性信号分子生长素[2]的不对称分布引起的,横向分布是由植物生长素转运蛋白PIN-FORMED3(PIN3)介导的下胚轴横向转运所产生的[3-5]。重力刺激将PIN3极化至内胚层细胞的底侧,这与受刺激器官下侧附近组织中生长素的积累增加有关,生长素会诱导细胞伸长,从而导致器官弯曲。曲率响应允许下胚轴以确定的角度[6]恢复笔直生长,这意味着在某些点恢复了生长素对称性以防止过度弯曲。在这里,我们提出了对导致热带反应终止的细胞和分子机制的初步见解。我们确定了关于PIN3极化的生长素反馈是恢复PIN3依赖性生长素流动对称性的基本机制。因此,两个机械上不同的PIN3极化事件会在重力响应的不同时间点重定向生长素通量:首先,重力介导的PIN3介导的生长素流向下胚轴侧流动,生长素逐渐积累并促进生长,随后PIN3极化到细胞的另一侧,耗尽最大的生长素以终止弯曲。因此,对PIN3晚期极化的遗传或药理学干预阻止了反应的终止并导致下胚轴过度弯曲。这一观察结果揭示了生长素反馈对PIN极性的作用在热带反应的终止中。

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    《Current Biology: CB》 |2016年第22期|共7页
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