The Warburg micro syndrome protein RAB3GAP1 modulates neuronal morphogenesis and interacts with axon elongation end ER-Golgi trafficking factors.

Abstract

RAB3GAP1 is GTPase activating protein localized to the ER and Golgi compartments. In humans, mutations in RAB3GAP1 are the most common cause of Warburg Micro syndrome, a neurodevelopmental disorder associated with intellectual disability, microcephaly, and agenesis of the corpus callosum. We found that downregulation of RAB3GAP1 leads to a reduction in neurite outgrowth and complexity in human stem cell derived neurons. To further define the cellular function of RAB3GAP1, we sought to identify novel interacting proteins. We used a combination of mass spectrometry, co-immunoprecipitation and colocalization analysis and identified two novel interactors of RAB3GAP1: the axon elongation factor Dedicator of cytokinesis 7 (DOCK7) and the TATA modulatory factor 1 (TMF1) a modulator of Endoplasmic Reticulum (ER) to Golgi trafficking. To define the relationship between RAB3GAP1 and its two novel interactors, we analyzed their localization to different subcellular compartments in neuronal and non-neuronal cells with loss of RAB3GAP1. We find that RAB3GAP1 is important for the sub-cellular localization of TMF1 and DOCK7 across different compartments of the Golgi and endoplasmic reticulum. In addition, we find that loss of function mutations in RAB3GAP1 lead to dysregulation of pathways that are activated in response to the cellular stress like ATF6, MAPK, and PI3-AKT signaling. In summary, our findings suggest a novel role for RAB3GAP1 in neurite outgrowth that could encompass the regulation of proteins that control axon elongation, ER-Golgi trafficking, as well as pathways implicated in response to cellular stress.

• Authors: Pankaj S Ghate, Janay M Vacharasin, Joseph A Ward, Duncan Nowling, Valerie Kay, Mara H Cowen, Mary-Kate Lawlor, Mikayla McCord, Hailey Xu, Esteban Carmona, Seon-Hye Cheon, Evelyn Chukwurah, Mike Walla, Sofia B Lizarraga
• Journal: Neurobiology of disease (Neurobiol Dis) Vol. 184 Pg. 106215 (08 2023) ISSN: 1095-953X [Electronic] United States
• PMID: 37385458 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural)
• Copyright: Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Chemical References

• rab3 GTP-Binding Proteins
• RAB3GAP1 protein, human

Topics

• Humans
• Intellectual Disability (genetics)
• Microcephaly (genetics)
• rab3 GTP-Binding Proteins (genetics, metabolism)
• Endoplasmic Reticulum (metabolism)
• Neurons (metabolism)
• Axons (metabolism)