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BEN3/BIG2 ARF GEF 参与拟南芥中转高尔基体网络/早期内体中 Brefeldin A 敏感的运输。

BEN3/BIG2 ARF GEF is Involved in Brefeldin A-Sensitive Trafficking at the trans-Golgi Network/Early Endosome in Arabidopsis thaliana.

机构信息

Department of Biological Science, Graduate School of Science, Osaka University, Osaka, 560-0043 Japan.

Institute of Science and Technology Austria (IST Austria), 3400 Klosterneuburg, Austria.

出版信息

Plant Cell Physiol. 2017 Oct 1;58(10):1801-1811. doi: 10.1093/pcp/pcx118.

DOI:10.1093/pcp/pcx118
PMID:29016942
Abstract

Membrane traffic at the trans-Golgi network (TGN) is crucial for correctly distributing various membrane proteins to their destination. Polarly localized auxin efflux proteins, including PIN-FORMED1 (PIN1), are dynamically transported between the endosomes and the plasma membrane (PM) in the plant cells. The intracellular trafficking of PIN1 protein is sensitive to the fungal toxin brefeldin A (BFA), which is known to inhibit guanine nucleotide exchange factors for ADP ribosylation factors (ARF GEFs) such as GNOM. However, the molecular details of the BFA-sensitive trafficking pathway have not been fully revealed. In a previous study, we identified an Arabidopsis mutant BFA-visualized endocytic trafficking defective 3 (ben3) which exhibited reduced sensitivity to BFA in terms of BFA-induced intracellular PIN1 agglomeration. Here, we show that BEN3 encodes a member of BIG family ARF GEFs, BIG2. BEN3/BIG2 tagged with fluorescent proteins co-localized with markers for the TGN/early endosome (EE). Inspection of conditionally induced de novo synthesized PIN1 confirmed that its secretion to the PM is BFA sensitive, and established BEN3/BIG2 as a crucial component of this BFA action at the level of the TGN/EE. Furthermore, ben3 mutation alleviated BFA-induced agglomeration of another TGN-localized ARF GEF, BEN1/MIN7. Taken together, our results suggest that BEN3/BIG2 is an ARF GEF component, which confers BFA sensitivity to the TGN/EE in Arabidopsis.

摘要

跨高尔基网络(TGN)的膜运输对于正确分配各种膜蛋白到其目的地至关重要。极性定位的生长素外排蛋白,包括 PIN 形成蛋白 1(PIN1),在植物细胞中在内体和质膜(PM)之间动态运输。PIN1 蛋白的细胞内运输对真菌毒素布雷菲德菌素 A(BFA)敏感,BFA 已知抑制 ADP 核糖基化因子(ARF)的鸟嘌呤核苷酸交换因子(ARF GEFs),如 GNOM。然而,BFA 敏感的运输途径的分子细节尚未完全揭示。在之前的一项研究中,我们鉴定了一个拟南芥突变体 BFA-可视化内吞运输缺陷 3(ben3),该突变体在 BFA 诱导的细胞内 PIN1 聚集方面对 BFA 的敏感性降低。在这里,我们表明 BEN3 编码 BIG 家族 ARF GEFs 的一个成员,BIG2。用荧光蛋白标记的 BEN3/BIG2 与 TGN/早期内体(EE)的标记物共定位。条件诱导新合成的 PIN1 的检查证实了其向 PM 的分泌对 BFA 敏感,并将 BEN3/BIG2 确立为该 BFA 在 TGN/EE 水平上作用的关键组成部分。此外,ben3 突变减轻了另一个 TGN 定位的 ARF GEF BEN1/MIN7 诱导的聚集。总之,我们的结果表明 BEN3/BIG2 是一个 ARF GEF 组成部分,它使拟南芥的 TGN/EE 对 BFA 敏感。

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