Stacks off tracks a role for the golgin AtCASP in plant endoplasmic reticulum-Golgi apparatus tethering

• Published in: Journal of experimental botany Vol. 68; no. 13; pp. 3339 - 3350
• Main Authors: Osterrieder, Anne, Sparkes, Imogen A., Botchway, Stan W., Ward, Andy, Ketelaar, Tijs, de Ruijter, Norbert, Hawes, Chris
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 15-06-2017
• Subjects: Arabidopsis - genetics; Arabidopsis - metabolism; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Cell Biology; Endoplasmic Reticulum - metabolism; EPS; Golgi Apparatus - metabolism; Golgi Matrix Proteins; Laboratorium voor Celbiologie; Laboratory of Cell Biology; Membrane Proteins - genetics; Membrane Proteins - metabolism; Plant Leaves - metabolism; Research Papers; tethering factor; Arabidopsis; optical tweezers; secretory pathway; golgin; endoplasmic reticulum; Golgi apparatus; endomembrane system
• ISSN: 0022-0957; 1460-2431; 1460-2431
• DOI: 10.1093/jxb/erx167

The plant Golgi apparatus modifies and sorts incoming proteins from the endoplasmic reticulum (ER) and synthesizes cell wall matrix material. Plant cells possess numerous motile Golgi bodies, which are connected to the ER by yet to be identified tethering factors. Previous studies indicated a role for cis-Golgi plant golgins, which are long coiled-coil domain proteins anchored to Golgi membranes, in Golgi biogenesis. Here we show a tethering role for the golgin AtCASP at the ER-Golgi interface. Using live-cell imaging, Golgi body dynamics were compared in Arabidopsis thaliana leaf epidermal cells expressing fluorescently tagged AtCASP, a truncated AtCASP-ΔCC lacking the coiled-coil domains, and the Golgi marker STtmd. Golgi body speed and displacement were significantly reduced in AtCASP-ΔCC lines. Using a dual-colour optical trapping system and a TIRF-tweezer system, individual Golgi bodies were captured in planta. Golgi bodies in AtCASP-ΔCC lines were easier to trap and the ER-Golgi connection was more easily disrupted. Occasionally, the ER tubule followed a trapped Golgi body with a gap, indicating the presence of other tethering factors. Our work confirms that the intimate ER-Golgi association can be disrupted or weakened by expression of truncated AtCASP-ΔCC and suggests that this connection is most likely maintained by a golgin-mediated tethering complex.