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PMID: 10748082 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Control of intramolecular interactions between the pleckstrin homology and Dbl homology domains of Vav and Sos1 regulates Rac binding.

The Journal of biological chemistry ·Vol. 275 ·No. 20 ·2000-05-19 ·Pages 15074-81

Das B, Shu X, Day GJ, Han J, Krishna UM, Falck JR, Broek D

Abstract

Vav and Sos1 are Dbl family guanine nucleotide exchange factors, which activate Rho family GTPases in response to phosphatidylinositol 3-kinase products. A pleckstrin homology domain adjacent to the catalytic Dbl homology domain via an unknown mechanism mediates the effects of phosphoinositides on guanine nucleotide exchange activity. Here we tested the possibility that phosphatidylinositol 3-kinase substrates and products control an interaction between the pleckstrin homology domain and the Dbl homology domain, thereby explaining the inhibitory effects of phosphatidylinositol 3-kinase substrates and stimulatory effects of the products. Binding studies using isolated fragments of Vav and Sos indicate phosphatidylinositol 3-kinase substrate promotes the binding of the pleckstrin homology domain to the Dbl homology domain and blocks Rac binding to the DH domain, whereas phosphatidylinositol 3-kinase products disrupt the Dbl homology/pleckstrin homology interactions and permit Rac binding. Additionally, Lck phosphorylation of Vav, a known activating event, reduces the affinities between the Vav Dbl homology and pleckstrin homology domains and permits Rac binding. We also show Vav activation in cells, as monitored by phosphorylation of Vav, Vav association with phosphatidylinositol 3,4,5-trisphosphate, and Vav guanine nucleotide exchange activity, is blocked by the phosphatidylinositol 3-kinase inhibitor wortmannin. These results suggest the molecular mechanisms for activation of Vav and Sos1 require disruption of inhibitory intramolecular interactions involving the pleckstrin homology and Dbl homology domains.

MeSH Terms
3T3 Cells Animals Binding Sites Cell Cycle Proteins Cloning, Molecular Escherichia coli Mice Phosphatidylinositol 3-Kinases/metabolism Phosphatidylinositol 4,5-Diphosphate/metabolism Phosphatidylinositol Phosphates/metabolism Phospholipids/metabolism Phosphorylation Proto-Oncogene Proteins/chemistry,metabolism Proto-Oncogene Proteins c-vav Recombinant Proteins/metabolism SOS1 Protein/chemistry,metabolism Transfection rac GTP-Binding Proteins/metabolism src Homology Domains
Chemicals
Cell Cycle Proteins Phosphatidylinositol 4,5-Diphosphate Phosphatidylinositol Phosphates Phospholipids Proto-Oncogene Proteins Proto-Oncogene Proteins c-vav Recombinant Proteins SOS1 Protein Vav1 protein, mouse phosphatidylinositol 3,4,5-triphosphate rac GTP-Binding Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Das B
Department of Biochemistry and Molecular Biology, Norris Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, California 90089, USA.
Shu X
Day G J
Han J
Krishna U M
Falck J R
Broek D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-05-19
Pages
15074-81
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA50261 · United States
NIGMS NIH HHS · GM31278 · United States
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