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A Rho Scaffold Integrates the Secretory System with Feedback Mechanisms in Regulation of Auxin Distribution

机译:Rho脚手架将分泌系统与反馈机制整合调节生长素的分布

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摘要

Development in multicellular organisms depends on the ability of individual cells to coordinate their behavior by means of small signaling molecules to form correctly patterned tissues. In plants, a unique mechanism of directional transport of the signaling molecule auxin between cells connects cell polarity and tissue patterning and thus is required for many aspects of plant development. Direction of auxin flow is determined by polar subcellular localization of PIN auxin efflux transporters. Dynamic PIN polar localization results from the constitutive endocytic cycling to and from the plasma membrane, but it is not well understood how this mechanism connects to regulators of cell polarity. The Rho family small GTPases ROPs/RACs are master regulators of cell polarity, however their role in regulating polar protein trafficking and polar auxin transport has not been established. Here, by analysis of mutants and transgenic plants, we show that the ROP interactor and polarity regulator scaffold protein ICR1 is required for recruitment of PIN proteins to the polar domains at the plasma membrane. icr1 mutant embryos and plants display an a array of severe developmental aberrations that are caused by compromised differential auxin distribution. ICR1 functions at the plasma membrane where it is required for exocytosis but does not recycle together with PINs. ICR1 expression is quickly induced by auxin but is suppressed at the positions of stable auxin maxima in the hypophysis and later in the embryonic and mature root meristems. Our results imply that ICR1 is part of an auxin regulated positive feedback loop realized by a unique integration of auxin-dependent transcriptional regulation into ROP-mediated modulation of cell polarity. Thus, ICR1 forms an auxin-modulated link between cell polarity, exocytosis, and auxin transport-dependent tissue patterning.
机译:多细胞生物的发展取决于单个细胞通过小的信号分子形成正确模式的组织来协调其行为的能力。在植物中,信号分子生长素在细胞之间定向运输的独特机制将细胞极性与组织模式连接在一起,因此对于植物发育的许多方面都是必需的。生长素流动的方向由PIN生长素外排转运蛋白的极性亚细胞定位确定。动态PIN极性定位是由与细胞质膜之间的本构内吞循环引起的,但对此机制如何与细胞极性调节剂连接尚不清楚。 Rho家族的小GTPases ROP / RAC是细胞极性的主要调节剂,但尚未确定其在调节极性蛋白质运输和极性植物生长素运输中的作用。在这里,通过分析突变体和转基因植物,我们表明ROP相互作用子和极性调节剂支架蛋白ICR1是将PIN蛋白募集到质膜极性域所必需的。 icr1突变体的胚胎和植物显示出一系列严重的发育异常,这些异常是由于生长素的差异性分布受损而引起的。 ICR1在胞吐作用所需的质膜上起作用,但不会与PIN一起回收。生长素可以快速诱导ICR1表达,但在垂体中稳定的生长素最大值位置会受到抑制,后来在胚胎和成熟的根分生组织中则被抑制。我们的结果表明,ICR1是生长素调节的正反馈环的一部分,该环通过将生长素依赖性转录调节独特地整合到ROP介导的细胞极性调节中而实现。因此,ICR1在细胞极性,胞吐作用和生长素依赖运输的组织构图之间形成生长素调节的联系。

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