Different Endomembrane Trafficking Pathways Establish Apical and Basal Polarities

内膜系统 生物 电池极性 细胞生物学 极性(国际关系) GTP酶 蛋白质靶向 膜蛋白 拟南芥 布雷菲尔德A 生物化学 突变体 细胞 内质网 基因 高尔基体
作者
Ruixi Li,Cecilia Rodríguez-Furlán,Junqi Wang,Wilhelmina van de Ven,Ting Gao,Natasha V. Raikhel,Glenn R. Hicks
出处
期刊:The Plant Cell [Oxford University Press]
卷期号:29 (1): 90-108 被引量:52
标识
DOI:10.1105/tpc.16.00524
摘要

The endomembrane system is an interconnected network required to establish signal transduction, cell polarity, and cell shape in response to developmental or environmental stimuli. In the model plant Arabidopsis thaliana, there are numerous markers to visualize polarly localized plasma membrane proteins utilizing endomembrane trafficking. Previous studies have shown that the large ARF-GEF GNOM plays a key role in the establishment of basal (rootward) polarity, whereas the apically (shootward) polarized membrane proteins undergo sorting via different routes. However, the mechanism that maintains apical polarity is largely unknown. Here, we used a chemical genomic approach and identified the compound endosidin 16 (ES16), which perturbed apically localized plasma membrane proteins without affecting basal polarity. We demonstrated that ES16 is an inhibitor for recycling of apical, lateral, and nonpolar plasma membrane proteins as well as biosynthetic secretion, leaving the basal proteins as the only exceptions not subject to ES16 inhibition. Further evidence from pharmaceutical and genetic data revealed that ES16 effects are mediated through the regulation of small GTPase RabA proteins and that RabA GTPases work in concert with the BIG clade ARF-GEF to modulate the nonbasal trafficking. Our results reveal that ES16 defines a distinct pathway for endomembrane sorting routes and is essential for the establishment of cell polarity.
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