Two SH2 domains of p120 Ras GTPase-activating protein bind synergistically to tyrosine phosphorylated p190 Rho GTPase-activating protein. 1995

S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
Cellular and Molecular Biology Program, University of Michigan Medical School, Ann Arbor 48109, USA.

p120 GTPase-activating protein (GAP) is a negative regulator of Ras that functions at a key relay point in signal transduction pathways that control cell proliferation. Among other proteins, p120 GAP associates with p190, a GAP for the Ras-related protein, Rho. To characterize the p120.p190 interaction further, we used bacterially expressed glutathione S-transferase fusion polypeptides to map the regions of p120 necessary for its interactions with p190. Our results show that both the N-terminal and the C-terminal SH2 domains of p120 are individually capable of binding p190 expressed in a baculovirus/insect cell system. Moreover, the two SH2 domains together on one polypeptide bind synergistically to p190, and this interaction is dependent on tyrosine phosphorylation of p190. In addition, mutation of the highly conserved Arg residues in the critical FLVR sequences of both SH2 domains of full-length p120 reduces binding to tyrosine-phosphorylated p190. The dependence on p190 phosphorylation for complex formation with p120 SH2 domains observed in vitro is consistent with analysis of the native p120.p190 complexes formed in vivo. These findings suggest that SH2-phosphotyrosine interaction is one mechanism by which the cell regulates p120.p190 association and thus may be a means for coordinating the Ras- and Rho-mediated signaling pathways.

UI MeSH Term Description Entries
D009687 Nuclear Proteins Proteins found in the nucleus of a cell. Do not confuse with NUCLEOPROTEINS which are proteins conjugated with nucleic acids, that are not necessarily present in the nucleus. Nucleolar Protein,Nucleolar Proteins,Nuclear Protein,Protein, Nuclear,Protein, Nucleolar,Proteins, Nuclear,Proteins, Nucleolar
D010750 Phosphoproteins Phosphoprotein
D010766 Phosphorylation The introduction of a phosphoryl group into a compound through the formation of an ester bond between the compound and a phosphorus moiety. Phosphorylations
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D011506 Proteins Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein. Gene Products, Protein,Gene Proteins,Protein,Protein Gene Products,Proteins, Gene
D012097 Repressor Proteins Proteins which maintain the transcriptional quiescence of specific GENES or OPERONS. Classical repressor proteins are DNA-binding proteins that are normally bound to the OPERATOR REGION of an operon, or the ENHANCER SEQUENCES of a gene until a signal occurs that causes their release. Repressor Molecules,Transcriptional Silencing Factors,Proteins, Repressor,Silencing Factors, Transcriptional
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D002460 Cell Line Established cell cultures that have the potential to propagate indefinitely. Cell Lines,Line, Cell,Lines, Cell
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
January 1995, Methods in enzymology,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
August 1992, Molecular and cellular biology,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
June 1996, The Journal of biological chemistry,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
July 1992, The Journal of biological chemistry,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
March 2009, Biochimie,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
October 2011, Cellular signalling,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
October 2009, Blood,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
June 2004, The Biochemical journal,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
November 2000, The Journal of biological chemistry,
S S Bryant, and S Briggs, and T E Smithgall, and G A Martin, and F McCormick, and J H Chang, and S J Parsons, and R Jove
December 1994, Science (New York, N.Y.),
Copied contents to your clipboard!