Literature DB >> 9438848

Role of substrates and products of PI 3-kinase in regulating activation of Rac-related guanosine triphosphatases by Vav.

J Han1, K Luby-Phelps, B Das, X Shu, Y Xia, R D Mosteller, U M Krishna, J R Falck, M A White, D Broek.   

Abstract

Mitogen stimulation of cytoskeletal changes and c-jun amino-terminal kinases is mediated by Rac small guanine nucleotide-binding proteins. Vav, a guanosine diphosphate (GDP)-guanosine triphosphate (GTP) exchange factor for Rac that stimulates the exchange of bound GDP for GTP, bound to and was directly controlled by substrates and products of phosphoinositide (PI) 3-kinase. The PI 3-kinase substrate phosphatidylinositol-4,5-bisphosphate inhibited activation of Vav by the tyrosine kinase Lck, whereas the product phosphatidylinositol-3,4,5-trisphosphate enhanced phosphorylation and activation of Vav by Lck. Control of Vav in response to mitogens by the products of PI 3-kinase suggests a mechanism for Ras-dependent activation of Rac.

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Year:  1998        PMID: 9438848     DOI: 10.1126/science.279.5350.558

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  200 in total

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Review 6.  Regulatory and signaling properties of the Vav family.

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Review 8.  Leukocytes navigate by compass: roles of PI3Kgamma and its lipid products.

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9.  Vav-2 controls NFAT-dependent transcription in B- but not T-lymphocytes.

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