Department of Plant Cell Biology, Centre for Organismal Biology, University of Heidelberg, Germany.
J Microsc. 2012 Jul;247(1):48-59. doi: 10.1111/j.1365-2818.2011.03597.x. Epub 2012 Feb 23.
The higher plant Golgi apparatus consists of hundreds of individual Golgi stacks which move along the cortical ER, propelled by the actomysin system. Anterograde and retrograde transport between the endoplasmic reticulum (ER) and the plant Golgi occurs over a narrow interface (around 500 nm) and is generally considered to be mediated by COP-coated vesicles. Previously, ER exit sites (ERES) have been identified on the basis of to localization of transiently expressed COPII-coat proteins. As a consequence it has been held that ERES in higher plants are intimately associated with Golgi stacks, and that both move together as an integrated structure: the "secretory unit". Using a new COPII marker, as well as YFP-SEC24 (a bona fide COPII coat protein), we have made observations on tobacco leaf epidermis at high resolution in the CLSM. Our data clearly shows that COPII fluorescence is associated with the Golgi stacks rather than the surface of the ER and probably represents the temporary accumulation of COPII vesicles in the Golgi matrix prior to fusion with the cis-Golgi cisternae. We have calculated the numbers of COPII vesicles which would be required to provide a typical Golgi-associated COPII-fluorescent signal as being much less than 20. We have discussed the consequences of this and question the continued usage of the term "secretory unit".
高等植物的高尔基体由数百个单独的高尔基体堆叠组成,这些堆叠沿着皮质内质网移动,由肌动蛋白系统推动。内质网 (ER) 和植物高尔基体之间的正向和逆向运输发生在一个狭窄的界面(约 500nm)上,通常被认为是由 COP 包被囊泡介导的。以前,根据瞬时表达的 COPII 外套蛋白的定位,已经确定了内质网出口部位 (ERES)。因此,人们认为高等植物中的 ERES 与高尔基体堆叠密切相关,并且它们作为一个集成结构一起移动:“分泌单元”。使用新的 COPII 标记物以及 YFP-SEC24(一种真正的 COPII 外套蛋白),我们在 CLSM 中以高分辨率对烟草叶表皮进行了观察。我们的数据清楚地表明,COPII 荧光与高尔基体堆叠相关,而不是与内质网的表面相关,并且可能代表 COPII 囊泡在与顺式高尔基体潴腔融合之前在高尔基体基质中的临时积累。我们计算了提供典型高尔基体相关 COPII 荧光信号所需的 COPII 囊泡的数量,结果表明数量远小于 20。我们讨论了这一结果的意义,并对继续使用“分泌单元”一词提出了质疑。