Independent yet overlapping pathways ensure the robustness and responsiveness of trans-Golgi network functions in Arabidopsis

Author:

Ravikumar Raksha1,Kalbfuß Nils1,Gendre Delphine2ORCID,Steiner Alexander1,Altmann Melina3,Altmann Stefan3,Rybak Katarzyna1ORCID,Edelmann Holger1,Stephan Friederike1,Lampe Marko4,Facher Eva5,Wanner Gerhard6ORCID,Falter-Braun Pascal37ORCID,Bhalerao Rishikesh P.2ORCID,Assaad Farhah F.1ORCID

Affiliation:

1. Plant Science Department, Botany, Technische Universität München, 85354 Freising, Germany

2. Umeå Plant Science Centre, Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, S-901 83 Umeå, Sweden

3. Institute of Network Biology (INET), Helmholtz Zentrum München, Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH), 85764 Neuherberg, Germany

4. Advanced Light Microscopy Facility, EMBL Heidelberg, 69117 Heidelberg, Germany

5. Systematic Botany and Mycology, Faculty of Biology, Dept. I Ludwig-Maximilians-Universität, 80638 Munich, Germany

6. Faculty of Biology, Dept. I, Ludwig-Maximillians Universität, 82152 Planegg-Martinsried, Germany

7. Faculty of Biology, Microbe-Host-Interactions, Ludwig-Maximilians-Universität (LMU) München, 82152 Planegg-Martinsried, Germany

Abstract

ABSTRACT The trans-Golgi-network (TGN) has essential housekeeping functions in secretion, endocytosis and protein sorting, but also more specialized functions in plant development. How the robustness of basal TGN function is ensured while specialized functions are differentially regulated is poorly understood. Here, we investigate two key regulators of TGN structure and function, ECHIDNA and the Transport Protein Particle II (TRAPPII) tethering complex. An analysis of physical, network and genetic interactions suggests that two network communities are implicated in TGN function and that ECHIDNA and TRAPPII belong to distinct yet overlapping pathways. Whereas ECHIDNA and TRAPPII colocalized at the TGN in interphase cells, their localization diverged in dividing cells. Moreover, ECHIDNA and TRAPPII localization patterns were mutually independent. TGN structure, endocytosis and sorting decisions were differentially impacted in echidna and trappii mutants. Our analyses point to a partitioning of specialized TGN functions, with ECHIDNA being required for cell elongation and TRAPPII for cytokinesis. Two independent pathways able to compensate for each other might contribute to the robustness of TGN housekeeping functions and to the responsiveness and fine tuning of its specialized functions.

Funder

Deutsche Forschungsgemeinschaft

Knut och Alice Wallenbergs Stiftelse

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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