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The E3 Ubiquitin Ligase SCFTIR1/AFB and Membrane Sterols Play Key Roles in Auxin Regulation of Endocytosis Recycling and Plasma Membrane Accumulation of the Auxin Efflux Transporter PIN2 in Arabidopsis thaliana

机译:E3泛素连接酶SCFTIR1 / AFB和膜甾醇在拟南芥生长素外排转运蛋白PIN2的内吞调节内吞再循环和血浆膜积累的生长素调节中起关键作用

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摘要

The PIN family of auxin efflux transporters exhibit polar plasma membrane (PM) localization and play a key role in auxin gradient-mediated developmental processes. Auxin inhibits PIN2 endocytosis and promotes its PM localization. However, the underlying mechanisms remain elusive. Here, we show that the inhibitory effect of auxin on PIN2 endocytosis was impaired in SCFTIR1/AFB auxin signaling mutants. Similarly, reducing membrane sterols impaired auxin inhibition of PIN2 endocytosis. Gas chromatography–mass spectrometry analyses indicate that membrane sterols were significantly reduced in SCFTIR1/AFB mutants, supporting a link between membrane sterols and auxin signaling in regulating PIN2 endocytosis. We show that auxin promoted PIN2 recycling from endosomes to the PM and increased PIN2 steady state levels in the PM fraction. Furthermore, we show that the positive effect of auxin on PIN2 levels in the PM was impaired by inhibiting membrane sterols or auxin signaling. Consistent with this, the sterol biosynthetic mutant fk-J79 exhibited pronounced defects in primary root elongation and gravitropic response. Our data collectively indicate that, although there are distinct processes involved in endocytic regulation of specific PM-resident proteins, the SCFTIR1/AFB-dependent processes are required for auxin regulation of endocytosis, recycling, and PM accumulation of the auxin efflux transporter PIN2 in Arabidopsis thaliana.
机译:生长素外排转运蛋白的PIN家族具有极性质膜(PM)定位,并在生长素梯度介导的发育过程中发挥关键作用。生长素抑制PIN2内吞并促进其PM定位。但是,基本机制仍然难以捉摸。在这里,我们表明生长素对PIN2内吞作用的抑制作用在SCF TIR1 / AFB 生长素信号转导突变体中被削弱。同样,减少膜固醇会损害生长素对PIN2内吞作用的抑制作用。气相色谱-质谱分析表明,SCF TIR1 / AFB 突变体中的膜固醇显着减少,支持膜固醇和生长素信号传导之间的联系,从而调节PIN2内吞作用。我们表明,生长素促进了PIN2从内体到PM的再循环,并增加了PM组分中PIN2的稳态水平。此外,我们表明,生长素对PM中PIN2水平的积极作用受到膜固醇或生长素信号传导的抑制。与此相一致,固醇生物合成突变体fk-J79在初生根伸长和重力反应中表现出明显的缺陷。我们的数据共同表明,尽管特定PM驻留蛋白的内吞调节涉及不同的过程,但生长素调节内吞,再循环和PM积累需要SCF TIR1 / AFB 依赖性过程拟南芥中植物生长素外排转运蛋白PIN2的表达。

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