daSilva Luis L P, Snapp Erik L, Denecke Jürgen, Lippincott-Schwartz Jennifer, Hawes Chris, Brandizzi Federica
Centre of Plant Sciences, University of Leeds, LS2 9JT, United Kingdom.
Plant Cell. 2004 Jul;16(7):1753-71. doi: 10.1105/tpc.022673. Epub 2004 Jun 18.
In contrast with animals, plant cells contain multiple mobile Golgi stacks distributed over the entire cytoplasm. However, the distribution and dynamics of protein export sites on the plant endoplasmic reticulum (ER) surface have yet to be characterized. A widely accepted model for ER-to-Golgi transport is based on the sequential action of COPII and COPI coat complexes. The COPII complex assembles by the ordered recruitment of cytosolic components on the ER membrane. Here, we have visualized two early components of the COPII machinery, the small GTPase Sar1p and its GTP exchanging factor Sec12p in live tobacco (Nicotiana tabacum) leaf epidermal cells. By in vivo confocal laser scanning microscopy and fluorescence recovery after photobleaching experiments, we show that Sar1p cycles on mobile punctate structures that track with the Golgi bodies in close proximity but contain regions that are physically separated from the Golgi bodies. By contrast, Sec12p is uniformly distributed along the ER network and does not accumulate in these structures, consistent with the fact that Sec12p does not become part of a COPII vesicle. We propose that punctate accumulation of Sar1p represents ER export sites (ERES). The sites may represent a combination of Sar1p-coated ER membranes, nascent COPII membranes, and COPII vectors in transit, which have yet to lose their coats. ERES can be induced by overproducing Golgi membrane proteins but not soluble bulk-flow cargos. Few punctate Sar1p loci were observed that are independent of Golgi bodies, and these may be nascent ERES. The vast majority of ERES form secretory units that move along the surface of the ER together with the Golgi bodies, but movement does not influence the rate of cargo transport between these two organelles. Moreover, we could demonstrate using the drug brefeldin A that formation of ERES is strictly dependent on a functional retrograde transport route from the Golgi apparatus.
与动物细胞不同,植物细胞含有多个移动的高尔基体堆叠,分布在整个细胞质中。然而,植物内质网(ER)表面蛋白质输出位点的分布和动态尚未得到表征。一种广泛接受的内质网到高尔基体运输模型是基于COPII和COPI衣被复合物的顺序作用。COPII复合物通过内质网膜上细胞溶质成分的有序募集而组装。在这里,我们在活的烟草(Nicotiana tabacum)叶表皮细胞中可视化了COPII机制的两个早期成分,小GTP酶Sar1p及其GTP交换因子Sec12p。通过体内共聚焦激光扫描显微镜和光漂白后荧光恢复实验,我们表明Sar1p在移动的点状结构上循环,这些结构与高尔基体紧密相邻并跟踪,但包含与高尔基体物理分离的区域。相比之下,Sec12p沿内质网网络均匀分布,并不在这些结构中积累,这与Sec12p不会成为COPII囊泡一部分的事实一致。我们提出Sar1p的点状积累代表内质网输出位点(ERES)。这些位点可能代表Sar1p包被的内质网膜、新生的COPII膜和正在运输的尚未失去衣被的COPII载体的组合。ERES可以通过过量表达高尔基体膜蛋白而不是可溶性大量运输货物来诱导。很少观察到独立于高尔基体的点状Sar1p位点,这些可能是新生的ERES。绝大多数ERES形成分泌单元,与高尔基体一起沿着内质网表面移动,但这种移动不会影响这两个细胞器之间货物运输的速率。此外,我们可以使用药物布雷菲德菌素A证明ERES的形成严格依赖于从高尔基体的功能性逆行运输途径。