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PMID: 15020670 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Rho-family GTPases: it's not only Rac and Rho (and I like it).

Journal of cell science ·Vol. 117 ·No. Pt 8 ·2004-03-15 ·Pages 1301-12

Wennerberg K, Der CJ

Abstract

The Rho-family proteins make up a major branch of the Ras superfamily of small GTPases. To date, 22 human genes encoding at least 25 proteins have been described. The best known 'classical' members are RhoA, Rac1 and Cdc42. Highly related isoforms of these three proteins have not been studied as intensively, in part because it has been assumed that they are functionally identical to their better-studied counterparts. This now appears not to be the case. Variations in C-terminal-signaled modifications and subcellular targeting cause otherwise highly biochemically related isoforms (e.g. RhoA, RhoB and RhoC) to exhibit surprisingly divergent biological activities. Whereas the classical Rho GTPases are regulated by GDP/GTP cycling, other Rho GTPases are also regulated by other mechanisms, particularly by transcriptional regulation. Newer members of the family possess additional sequence elements beyond the GTPase domain, which suggests they exhibit yet other mechanisms of regulation.

MeSH Terms
Amino Acid Motifs Amino Acid Sequence Gene Expression Regulation, Enzymologic Humans Models, Biological Molecular Sequence Data Phylogeny Protein Processing, Post-Translational Protein Structure, Tertiary Sequence Homology, Amino Acid cdc42 GTP-Binding Protein/genetics,metabolism rac1 GTP-Binding Protein/genetics,metabolism rho GTP-Binding Proteins/chemistry,metabolism rhoA GTP-Binding Protein/genetics,metabolism
Chemicals
cdc42 GTP-Binding Protein rac1 GTP-Binding Protein rho GTP-Binding Proteins rhoA GTP-Binding Protein
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wennerberg Krister
Department of Pharmacology and Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7295, USA. kirster@med.unc.edu
Der Channing J
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
2004-03-15
Pages
1301-12
Language
English
Region
England
NLM ID
0052457
Subset
IM
Grants
NCI NIH HHS · CA63071 · United States
NCI NIH HHS · CA67771 · United States
NCI NIH HHS · CA92240 · United States
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