Abstract
DBC2 is a tumor suppressor gene linked to breast and lung cancers. Although DBC2 belongs to the RHO GTPase family, it has a unique structure that contains a Broad-Complex/Tramtrack/Bric a Brac (BTB) domain at the C terminus instead of a typical CAAX motif. A limited number of functional studies on DBC2 have indicated its participation in diverse cellular activities, such as ubiquitination, cell-cycle control, cytoskeleton organization and protein transport. In this study, the role of DBC2 in protein transport was analyzed using vesicular stomatitis virus glycoprotein (VSVG) fused with green fluorescent protein. We discovered that DBC2 knockdown hinders the VSVG transport system in 293 cells. Previous studies have demonstrated that VSVG is transported via the microtubule motor complex. We demonstrate that DBC2 mobility depends also on an intact microtubule network. We conclude that DBC2 plays an essential role in microtubule-mediated VSVG transport from the endoplasmic reticulum to the Golgi apparatus.
MeSH Terms
Amino Acid Motifs
Cell Line
Endoplasmic Reticulum/metabolism
GTP-Binding Proteins/genetics,physiology
Golgi Apparatus/metabolism
Guanosine Triphosphate/metabolism
Humans
Membrane Glycoproteins/physiology
Microtubules/metabolism
Protein Transport
Recombinant Fusion Proteins/physiology
Tumor Suppressor Proteins/genetics,physiology
Viral Envelope Proteins/physiology
Chemicals
G protein, vesicular stomatitis virus
Membrane Glycoproteins
RHOBTB2 protein, human
Recombinant Fusion Proteins
Tumor Suppressor Proteins
Viral Envelope Proteins
Guanosine Triphosphate
GTP-Binding Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Chang Faith K
Department of Biological Sciences, Fordham University, 441 E Fordham Road, Bronx, NY 10458, USA.
Sato Noriko
Kobayashi-Simorowski Noriko
Yoshihara Takashi
Meth Jennifer L
Hamaguchi Masaaki
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