The CDC42 homologue from Caenorhabditis elegans. Complementation of yeast mutation
- PMID: 8514766
The CDC42 homologue from Caenorhabditis elegans. Complementation of yeast mutation
Abstract
A Caenorhabditis elegans cDNA encoding a homologue of the p21 ras-related CDC42, designated as CDC42Ce, was isolated from a nematode mixed stage cDNA library. The encoded protein of 188 amino acid residues has 85% identity to both human G25K and CDC42Hs and 79 and 76% identity to the yeast CDC42Sp and CDC42Sc proteins, respectively. The CDC42Ce cDNA maps to a position on C. elegans chromosome II in close proximity to lin-26, a cell lineage gene. The CDC42Ce cDNA hybridizes to 2- and 1.5-kilobase mRNAs. Their expression is developmentally regulated with highest levels at the embryonic stage, decreasing progressively during development except for an increase of the more abundant 1.5-kilobase mRNA at the L3 stage. The glutathione S-transferase/CDC42Ce fusion protein expressed in Escherichia coli displays both GTP binding and intrinsic GTPase activities. The GTPase activity of CDC42Ce is moderately stimulated by human n-chimaerin, a GTPase-activating protein for the related p21 rac1. The CDC42Ce protein complements the temperature-sensitive lethal mutation cdc42-1 in yeast Saccharomyces cerevisiae. These data suggest that CDC42Ce is the C. elegans homologue of the yeast CDC42. The developmental expression pattern of mRNA and is biochemical properties of its encoded protein which are closely related to CErac1 suggest that the two p21s might be involved in related biological processes.
Similar articles
-
A new member of the ras superfamily, the rac1 homologue from Caenorhabditis elegans. Cloning and sequence analysis of cDNA, pattern of developmental expression, and biochemical characterization of the protein.J Biol Chem. 1993 Jan 5;268(1):320-4. J Biol Chem. 1993. PMID: 7677998
-
The Caenorhabditis elegans p21-activated kinase (CePAK) colocalizes with CeRac1 and CDC42Ce at hypodermal cell boundaries during embryo elongation.J Biol Chem. 1996 Oct 18;271(42):26362-8. doi: 10.1074/jbc.271.42.26362. J Biol Chem. 1996. PMID: 8824291
-
Molecular cloning of the gene for the human placental GTP-binding protein Gp (G25K): identification of this GTP-binding protein as the human homolog of the yeast cell-division-cycle protein CDC42.Proc Natl Acad Sci U S A. 1990 Dec;87(24):9853-7. doi: 10.1073/pnas.87.24.9853. Proc Natl Acad Sci U S A. 1990. PMID: 2124704 Free PMC article.
-
Ras-regulated signaling processes in Saccharomyces cerevisiae.Curr Opin Genet Dev. 1991 Oct;1(3):370-7. doi: 10.1016/s0959-437x(05)80302-8. Curr Opin Genet Dev. 1991. PMID: 1668647 Review.
-
Regulation of phosphorylation pathways by p21 GTPases. The p21 Ras-related Rho subfamily and its role in phosphorylation signalling pathways.Eur J Biochem. 1996 Dec 1;242(2):171-85. doi: 10.1111/j.1432-1033.1996.0171r.x. Eur J Biochem. 1996. PMID: 8973630 Review.
Cited by
-
Molecular cloning, characterization and differential expression of Cdc42 in Fonsecaea monophora.Mol Biol Rep. 2012 Feb;39(2):839-44. doi: 10.1007/s11033-011-0806-2. Epub 2011 May 15. Mol Biol Rep. 2012. PMID: 21573800
-
Pheromone signalling in Saccharomyces cerevisiae requires the small GTP-binding protein Cdc42p and its activator CDC24.Mol Cell Biol. 1995 Oct;15(10):5246-57. doi: 10.1128/MCB.15.10.5246. Mol Cell Biol. 1995. PMID: 7565673 Free PMC article.
-
Adherens junctions in C. elegans embryonic morphogenesis.Subcell Biochem. 2012;60:279-99. doi: 10.1007/978-94-007-4186-7_12. Subcell Biochem. 2012. PMID: 22674076 Free PMC article. Review.
-
Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model.Sci Rep. 2019 Mar 14;9(1):4418. doi: 10.1038/s41598-019-40988-7. Sci Rep. 2019. PMID: 30872706 Free PMC article.
-
Suppressors of the unc-73 gene of Caenorhabditis elegans.Genetics. 1996 May;143(1):225-36. doi: 10.1093/genetics/143.1.225. Genetics. 1996. PMID: 8722777 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
Miscellaneous