1. Academic Validation
  2. RAB21 interacts with TMED10 and modulates its localization and abundance

RAB21 interacts with TMED10 and modulates its localization and abundance

  • Biol Open. 2019 Sep 9;8(9):bio045336. doi: 10.1242/bio.045336.
Tomas Del Olmo 1 Camille Lacarrière-Keïta 1 Caroline Normandin 1 Dominique Jean 1 François-Michel Boisvert 1 Steve Jean 2
Affiliations

Affiliations

  • 1 Faculté de Médecine et des Sciences de la Santé, Département d'anatomie et de biologie cellulaire, Université de Sherbrooke, 3201, Rue Jean Mignault, Sherbrooke, Québec, Canada J1E 4K8.
  • 2 Faculté de Médecine et des Sciences de la Santé, Département d'anatomie et de biologie cellulaire, Université de Sherbrooke, 3201, Rue Jean Mignault, Sherbrooke, Québec, Canada J1E 4K8 [email protected].
Abstract

Membrane trafficking controls vesicular transport of cargo between cellular compartments. Vesicular trafficking is essential for cellular homeostasis and dysfunctional trafficking is linked to several pathologies such as neurodegenerative diseases. Following endocytosis, early endosomes act as sorting stations of internalized Materials, routing cargo toward various fates. One important class of membrane trafficking regulators are RAB GTPases. RAB21 has been associated with multiple functions and regulates Integrin internalization, endosomal sorting of specific clathrin-independent cargo and Autophagy. Although RAB21 is mostly associated with early endosomes, it has been shown to mediate a specific sorting event at the Golgi. From mass spectrometry data, we identified a GTP-favored interaction between RAB21 and TMED10 and 9, essential regulators of COPI and COPII vesicles. Using RAB21 knockout cells, we describe the role of RAB21 in modulating TMED10 Golgi localization. Taken together, our study suggests a new potential function of RAB21 in modulating TMED10 trafficking, with relevance to neurodegenerative disorders.

Keywords

Membrane trafficking; TMED2; TMED9; p24 family.

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