Boevink P, Oparka K, Santa Cruz S, Martin B, Betteridge A, Hawes C
Unit of Cell Biology, Scottish Crop Research Institute, Invergowrie, Dundee, UK.
Plant J. 1998 Aug;15(3):441-7. doi: 10.1046/j.1365-313x.1998.00208.x.
We have visualized the relationship between the endoplasmic reticulum (ER) and Golgi in leaf cells of Nicotiana clevelandii by expression of two Golgi proteins fused to green fluorescent protein (GFP). A fusion of the transmembrane domain (signal anchor sequence) of a rat sialyl transferase to GFP was targeted to the Golgi stacks. A second construct that expressed the Arabidopsis H/KDEL receptor homologue aERD2, fused to GFP, was targeted to both the Golgi apparatus and ER, allowing the relationship between these two organelles to be studied in living cells for the first time. The Golgi stacks were shown to move rapidly and extensively along the polygonal cortical ER network of leaf epidermal cells, without departing from the ER tubules. Co-localization of F-actin in the GFP-expressing cells revealed an underlying actin cytoskeleton that matched precisely the architecture of the ER network, while treatment of cells with the inhibitors cytochalasin D and N-ethylmaleimide revealed the dependency of Golgi movement on actin cables. These observations suggest that the leaf Golgi complex functions as a motile system of actin-directed stacks whose function is to pick up products from a relatively stationary ER system. Also, we demonstrate for the first time in vivo brefeldin A-induced retrograde transport of Golgi membrane protein to the ER.
通过表达两种与绿色荧光蛋白(GFP)融合的高尔基体蛋白,我们观察了克利夫兰烟草叶片细胞内质网(ER)与高尔基体之间的关系。大鼠唾液酸转移酶的跨膜结构域(信号锚定序列)与GFP的融合蛋白定位于高尔基体堆叠。另一个构建体表达与GFP融合的拟南芥H/KDEL受体同源物aERD2,它定位于高尔基体和内质网,从而首次能够在活细胞中研究这两个细胞器之间的关系。结果显示,高尔基体堆叠沿着叶片表皮细胞的多边形皮质内质网网络快速且广泛地移动,且不脱离内质网管。在表达GFP的细胞中,F-肌动蛋白的共定位揭示了一个潜在的肌动蛋白细胞骨架,其与内质网网络的结构精确匹配,而用细胞松弛素D和N-乙基马来酰亚胺抑制剂处理细胞则揭示了高尔基体运动对肌动蛋白丝束的依赖性。这些观察结果表明,叶片高尔基体复合体作为一个由肌动蛋白引导的堆叠的运动系统发挥作用,其功能是从相对静止的内质网系统中获取产物。此外,我们首次在体内证明了布雷菲德菌素A诱导的高尔基体膜蛋白向内质网的逆行运输。