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PIN 生长素外排载体的极性由 PINOID 激酶介导的募集到 GNOM 非依赖性运输中调节在拟南芥中。

PIN auxin efflux carrier polarity is regulated by PINOID kinase-mediated recruitment into GNOM-independent trafficking in Arabidopsis.

机构信息

Department of Plant Systems Biology, Flanders Institute for Biotechnology, B-9052 Gent, Belgium.

出版信息

Plant Cell. 2009 Dec;21(12):3839-49. doi: 10.1105/tpc.109.071639. Epub 2009 Dec 29.

Abstract

The phytohormone auxin plays a major role in embryonic and postembryonic plant development. The temporal and spatial distribution of auxin largely depends on the subcellular polar localization of members of the PIN-FORMED (PIN) auxin efflux carrier family. The Ser/Thr protein kinase PINOID (PID) catalyzes PIN phosphorylation and crucially contributes to the regulation of apical-basal PIN polarity. The GTP exchange factor on ADP-ribosylation factors (ARF-GEF), GNOM preferentially mediates PIN recycling at the basal side of the cell. Interference with GNOM activity leads to dynamic PIN transcytosis between different sides of the cell. Our genetic, pharmacological, and cell biological approaches illustrate that PID and GNOM influence PIN polarity and plant development in an antagonistic manner and that the PID-dependent PIN phosphorylation results in GNOM-independent polar PIN targeting. The data suggest that PID and the protein phosphatase 2A not only regulate the static PIN polarity, but also act antagonistically on the rate of GNOM-dependent polar PIN transcytosis. We propose a model that includes PID-dependent PIN phosphorylation at the plasma membrane and the subsequent sorting of PIN proteins to a GNOM-independent pathway for polarity alterations during developmental processes, such as lateral root formation and leaf vasculature development.

摘要

植物激素生长素在胚胎和胚胎后植物发育中起着重要作用。生长素的时空分布在很大程度上取决于 PIN 形成素(PIN)生长素外排载体家族成员的亚细胞极性定位。丝氨酸/苏氨酸蛋白激酶 PINOID(PID)催化 PIN 的磷酸化,对调节顶端-基极 PIN 极性至关重要。ADP-核糖基化因子(ARF-GEF)上的 GTP 交换因子 GNOM 优先介导细胞底部的 PIN 循环。干扰 GNOM 活性会导致 PIN 在细胞不同侧之间的动态胞吞作用。我们的遗传、药理学和细胞生物学方法表明,PID 和 GNOM 以拮抗的方式影响 PIN 极性和植物发育,并且 PID 依赖性的 PIN 磷酸化导致与 GNOM 无关的极性 PIN 靶向。这些数据表明,PID 和蛋白磷酸酶 2A 不仅调节静态 PIN 极性,而且还在 GNOM 依赖性极性 PIN 胞吞作用的速率上起拮抗作用。我们提出了一个模型,其中包括质膜上的 PID 依赖性 PIN 磷酸化,以及随后将 PIN 蛋白分拣到一个与 GNOM 无关的途径,以在发育过程中改变极性,例如侧根形成和叶片脉管系统发育。

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