Rakusová Hana, Abbas Mohamad, Han Huibin, Song Siyuan, Robert Hélène S, Friml Jiří
Institute of Science and Technology (IST) Austria, 3400 Klosterneuburg, Austria; Department of Plant Systems Biology, VIB and Department of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Gent, Belgium.
Institute of Science and Technology (IST) Austria, 3400 Klosterneuburg, Austria.
Curr Biol. 2016 Nov 21;26(22):3026-3032. doi: 10.1016/j.cub.2016.08.067. Epub 2016 Oct 20.
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.
植物根据重力调整其生长。向重力性涉及重力感知、信号转导和不对称生长反应,结果是器官弯曲[1]。不对称生长源于植物特异性信号分子生长素的不对称分布[2],生长素通过侧向运输产生,在下胚轴中主要由生长素转运蛋白PIN-FORMED3(PIN3)介导[3-5]。重力刺激使PIN3极化到内皮层细胞的底部,这与受刺激器官下侧相邻组织中生长素积累增加相关,生长素在该部位诱导细胞伸长,进而导致器官弯曲。弯曲反应使下胚轴以特定角度恢复直立生长[6],这意味着在某个时刻生长素对称性得以恢复以防止过度弯曲。在此,我们对导致向性反应终止的细胞和分子机制进行了初步研究。我们发现生长素对PIN3极化的反馈是恢复PIN3依赖性生长素流对称性的潜在机制。因此,两个机制不同的PIN3极化事件在重力反应的不同时间点重定向生长素流:首先,重力介导PIN3介导的生长素流向在下胚轴下侧,生长素逐渐积累并促进生长,随后PIN3极化到相对的细胞一侧,耗尽生长素最大值以结束弯曲。相应地,对后期PIN3极化的遗传或药理学干扰会阻止反应终止并导致下胚轴过度弯曲。这一观察结果揭示了生长素对PIN极性的反馈在向性反应终止中的作用。