Atypical Rho GTPases of the RhoBTB Subfamily: Roles in vesicle trafficking and tumorigenesis

Ji, Wei; Rivero, Francisco

Abstract

RhoBTB proteins constitute a subfamily of atypical Rho GTPases represented in mammals by RhoBTB1, RhoBTB2, and RhoBTB3. Their characteristic feature is a carboxyl terminal extension that harbors two BTB domains capable of assembling cullin 3-dependent ubiquitin ligase complexes. The expression of all three RHOBTB genes has been found reduced or abolished in a variety of tumors. They are considered tumor suppressor genes and recent studies have strengthened their implication in tumorigenesis through regulation of the cell cycle and apoptosis. RhoBTB3 is also involved in retrograde transport from endosomes to the Golgi apparatus. One aspect that makes RhoBTB proteins atypical among the Rho GTPases is their proposed mechanism of activation. No specific guanine nucleotide exchange factors or GTPase activating proteins are known. Instead, RhoBTB might be activated through interaction with other proteins that relieve their auto-inhibited conformation and inactivated through auto-ubiquitination and destruction in the proteasome. In this review we discuss our current knowledge on the molecular mechanisms of action of RhoBTB proteins and the implications for tumorigenesis and other pathologic conditions.

Citation

Ji, W., & Rivero, F. (2016). Atypical Rho GTPases of the RhoBTB Subfamily: Roles in vesicle trafficking and tumorigenesis. Cells, 5(2), 28. https://doi.org/10.3390/cells5020028

• Journal Article Type: Review
• Acceptance Date: Jun 8, 2016
• Online Publication Date: Jun 14, 2016
• Publication Date: Jun 14, 2016
• Deposit Date: Jun 10, 2016
• Publicly Available Date: Oct 27, 2022
• Journal: Cells
• Electronic ISSN: 2073-4409
• Publisher: MDPI
• Peer Reviewed: Peer Reviewed
• Volume: 5
• Issue: 2
• Article Number: ARTN 28
• Pages: 28
• DOI: https://doi.org/10.3390/cells5020028
• Keywords: Cullin, Cyclin E, HIFα, Rab9, RhoBTB, Tumor suppressor, Ubiquitination
• Public URL: https://hull-repository.worktribe.com/output/439437
• Publisher URL: http://www.mdpi.com/2073-4409/5/2/28
• Additional Information: This is a copy of an article published in: Cells, 2016, v.5 issue 2.