Rho family proteins and Ras transformation: the RHOad less traveled gets congested
Abstract
The Rho family of small GTPases has attracted considerable research interest over the past 5 years. During this time, we have witnessed a remarkable increase in our knowledge of the biochemistry and biology of these Ras-related proteins. Thus, Rho family proteins have begun to rival, if not overshadow, interest in their more celebrated cousins, the Ras oncogene proteins. The fascination in Rho family proteins is fueled primarily by two major observations. First, like Ras, Rho family proteins serve as guanine nucleotide-regulated binary switches that control signaling pathways that in turn regulate diverse cellular processes. Rho family proteins are key components in cellular processes that control the organization of the actin cytoskeleton, activate kinase cascades, regulate gene expression, regulate membrane trafficking, promote growth transformation and induce apoptosis. Second, at least five Rho family proteins have been implicated as critical regulators of oncogenic Ras transformation. Thus, it is suspected that Rho family proteins contribute significantly to the aberrant growth properties of Ras-transformed cells. Rho family proteins are also critical mediators of the transforming actions of other transforming proteins and include Dbl family oncogene proteins, G protein-coupled receptors and G protein alpha subunits. Thus, Rho family proteins may be key components for the transforming actions of diverse oncogene proteins. Major aims of Rho family protein studies are to d…
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RhoH has no intrinsic GTPase activity.
“Due to the mutation of the conserved residues G13 and Q61 which are essential for hydrolysis of GTP, it was proposed that RhoH has no intrinsic GTPase activity [12,13].”
From The small GTPase RhoH is an atypical regulator of haematopoietic cells (2008) · cites this paper as [12]
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- Authors
- Zohn, I. M., Campbell, S. L., Khosravi-Far, R., Rossman, K. L., & Der, C. J.
- Affiliations
- Massachusetts Institute of Technology (US)
- University of North Carolina at Chapel Hill (US)
- Venue
- Oncogene
- Published
- 1998-09-17
- Volume
- 17
- Issue
- 11
- Pages
- 1415-1438
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W2001626727
- Cited by
- 352
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 4 · 2018: 2 · 2017: 3 · 2016: 5 · 2015: 3 · 2014: 2 · 2013: 5 · 2012: 6
- FWCI
- 15.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (7r01ca055008-03, 5r01ca042978-30, 5r01ca052072-05)
- National Cancer Institute (CA42978, CA 55008, CA52072)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- Rho GTPases, Ras transformation, oncogenic Ras, actin cytoskeleton organization, kinase cascade, membrane trafficking, apoptosis, G protein-coupled receptors, G protein alpha subunit, small GTPase signaling
- MeSH terms
- Actins, Amino Acid Sequence, Animals, Cell Division, Cell Movement, Cell Transformation, Neoplastic, Gene Expression Regulation, Humans, Molecular Sequence Data, Proto-Oncogene Proteins, Genes, ras, Retroviridae Proteins, Oncogenic, ras Proteins, GTP-Binding Proteins, GTP Phosphohydrolases, Guanine Nucleotide Exchange Factors, rhoA GTP-Binding Protein
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