Abstract

The trans-Golgi network (TGN) has been known as a key platform to sort and transport proteins to their final destinations in post-Golgi membrane trafficking. However, how the TGN sorts proteins with different destinies still remains elusive. Here, we examined 3D localization and 4D dynamics of TGN-localized proteins of Arabidopsis thaliana that are involved in either secretory or vacuolar trafficking from the TGN, by a multicolor high-speed and high-resolution spinning-disk confocal microscopy approach that we developed. We demonstrate that TGN-localized proteins exhibit spatially and temporally distinct distribution. VAMP721 (R-SNARE), AP (adaptor protein complex)−1, and clathrin which are involved in secretory trafficking compose an exclusive subregion, whereas VAMP727 (R-SNARE) and AP-4 involved in vacuolar trafficking compose another subregion on the same TGN. Based on these findings, we propose that the single TGN has at least two subregions, or “zones”, responsible for distinct cargo sorting: the secretory-trafficking zone and the vacuolar-trafficking zone.

The trans-Golgi network (TGN) serves as a platform to sort and transport proteins to their final destinations. Here the authors show that the TGN of Arabidopsis consists of spatially and temporally distinct subregions and propose that these zones may sort cargo to different destinations.

Details

Title
Cargo sorting zones in the trans-Golgi network visualized by super-resolution confocal live imaging microscopy in plants
Author
Shimizu Yutaro 1 ; Takagi Junpei 2   VIAFID ORCID Logo  ; Ito Emi 3 ; Ito Yoko 4   VIAFID ORCID Logo  ; Ebine Kazuo 5 ; Komatsu Yamato 6 ; Goto Yumi 7 ; Sato Mayuko 7   VIAFID ORCID Logo  ; Toyooka Kiminori 7   VIAFID ORCID Logo  ; Ueda, Takashi 5   VIAFID ORCID Logo  ; Kurokawa Kazuo 8 ; Uemura Tomohiro 3   VIAFID ORCID Logo  ; Nakano Akihiko 9   VIAFID ORCID Logo 

 RIKEN Center for Advanced Photonics, Wako, Live Cell Super-Resolution Imaging Research Team, Saitama, Japan; The University of Tokyo, Department of Biological Sciences, Graduate School of Science, Bunkyo-ku, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X) 
 Konan University, Kobe, Faculty of Science and Engineering, Hyogo, Japan (GRID:grid.258669.6) (ISNI:0000 0000 8565 5938) 
 Ochanomizu University, Graduate School of Humanities and Sciences, Bunkyo-ku, Japan (GRID:grid.412314.1) (ISNI:0000 0001 2192 178X) 
 RIKEN Center for Advanced Photonics, Wako, Live Cell Super-Resolution Imaging Research Team, Saitama, Japan (GRID:grid.412314.1); UMR 5200, CNRS, Université de Bordeaux, Laboratoire de Biogenèse Membranaire, Villenave d’Ornon, France (GRID:grid.4444.0) (ISNI:0000 0001 2112 9282) 
 National Institute for Basic Biology, Division of Cellular Dynamics, Okazaki, Japan (GRID:grid.419396.0) (ISNI:0000 0004 0618 8593); SOKENDAI (The Graduate University for Advanced Studies), The Department of Basic Biology, Okazaki, Japan (GRID:grid.275033.0) (ISNI:0000 0004 1763 208X) 
 The University of Tokyo, Department of Biological Sciences, Graduate School of Science, Bunkyo-ku, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X) 
 Mass Spectrometry and Microscopy Unit, RIKEN Center for Sustainable Resource Science, Technology Platform Division, Yokohama, Japan (GRID:grid.7597.c) (ISNI:0000000094465255) 
 RIKEN Center for Advanced Photonics, Wako, Live Cell Super-Resolution Imaging Research Team, Saitama, Japan (GRID:grid.275033.0) 
 RIKEN Center for Advanced Photonics, Wako, Live Cell Super-Resolution Imaging Research Team, Saitama, Japan (GRID:grid.412314.1) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2505573515
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.