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内质网导入部位及其与内质网出口部位的关系:高等植物中内质网-高尔基体逆向运输的新模型。

ER Import Sites and Their Relationship to ER Exit Sites: A New Model for Bidirectional ER-Golgi Transport in Higher Plants.

机构信息

Department of Plant Cell Biology, Centre for Organismal Studies, University of Heidelberg Heidelberg, Germany.

出版信息

Front Plant Sci. 2012 Jul 2;3:143. doi: 10.3389/fpls.2012.00143. eCollection 2012.

Abstract

Per definition, ER exit sites are COPII vesiculation events at the surface of the ER and in higher plants are only visualizable in the electron microscope through cryofixation techniques. Fluorescent COPII labeling moves with Golgi stacks and locates to the interface between the ER and the Golgi. In contrast, the domain of the ER where retrograde COPI vesicles fuse, i.e., ER import sites (ERIS), has remained unclear. To identify ERIS we have employed ER-located SNAREs and tethering factors. We screened several SNAREs (SYP81, the SYP7 family, and USE1) to find a SNARE whose overexpression did not disrupt ER-Golgi traffic and which gave rise to discrete fluorescent punctae when expressed with an XFP tag. Only the Qc-SNARE SYP72 fulfilled these criteria. When coexpressed with SYP72-YFP, both the type I-membrane protein RFP-p24δ5 and the luminal marker CFP-HDEL whose ER localization are due to an efficient COPI-mediated recycling, form nodules along the tubular ER network. SYP72-YFP colocalizes with these nodules which are not seen when RFP-p24δ5 or CFP-HDEL is expressed alone or when SYP72-YFP is coexpressed with a mutant form of RFP-p24δ5 that cannot exit the ER. SYP72-YFP does not colocalize with Golgi markers, except when the Golgi stacks are immobilized through actin depolymerization. Endogenous SYP7 SNAREs, also colocalize with immobilized COPII/Golgi. In contrast, XFP-tagged versions of plant homologs to TIP20 of the Dsl1 COPI-tethering factor complex, and the COPII-tethering factor p115 colocalize perfectly with Golgi stacks irrespective of the motile status. These data suggest that COPI vesicle fusion with the ER is restricted to periods when Golgi stacks are stationary, but that when moving both COPII and COPI vesicles are tethered and collect in the ER-Golgi interface. Thus, the Golgi stack and an associated domain of the ER thereby constitute a mobile secretory and recycling unit: a unique feature in eukaryotic cells.

摘要

根据定义,内质网出口部位是内质网上的 COPII 小泡化事件,在高等植物中,只有通过冷冻固定技术才能在电子显微镜下观察到。荧光 COPII 标记与高尔基体堆栈一起移动,并定位在内质网与高尔基体之间的界面处。相比之下,逆行 COPI 小泡融合的内质网区域,即内质网导入部位(ERIS),仍然不清楚。为了识别 ERIS,我们使用了内质网定位的 SNARE 和 tethering 因子。我们筛选了几种 SNARE(SYP81、SYP7 家族和 USE1),找到了一种 SNARE,其过表达不会破坏内质网-高尔基体运输,并且当与 XFP 标签表达时,会产生离散的荧光斑点。只有 Qc-SNARE SYP72 符合这些标准。当与 SYP72-YFP 共表达时,I 型膜蛋白 RFP-p24δ5 和 luminal 标记物 CFP-HDEL,其内质网定位是由于有效的 COPI 介导的回收,沿管状内质网网络形成结节。SYP72-YFP 与这些结节共定位,当 RFP-p24δ5 或 CFP-HDEL 单独表达或与不能从内质网输出的 RFP-p24δ5 的突变形式共表达时,不会看到这些结节。SYP72-YFP 与高尔基标记物不共定位,除非通过肌动蛋白解聚使高尔基堆栈固定。内源性 SYP7 SNARE 也与固定的 COPII/高尔基共定位。相比之下,植物同源物 XFP 标记版本的 Dsl1 COPI 连接因子复合物的 TIP20 和 COPII 连接因子 p115,与高尔基体堆栈完全共定位,无论其运动状态如何。这些数据表明,COPII 小泡与内质网的融合仅限于高尔基体堆栈静止的时期,但当移动时,COPII 和 COPI 小泡都被连接并收集在内质网-高尔基体界面处。因此,高尔基体堆栈和相关的内质网区域构成了一个可移动的分泌和回收单元:这是真核细胞的一个独特特征。

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