Matches in SemOpenAlex for { <https://semopenalex.org/work/W2154683723> ?p ?o ?g. }
- W2154683723 endingPage "9224" @default.
- W2154683723 startingPage "9212" @default.
- W2154683723 abstract "ABSTRACT A recently reported new member of the Vav family proteins, Vav3 has been identified as a Ros receptor protein tyrosine kinase (RPTK) interacting protein by yeast two-hybrid screening. Northern analysis shows that Vav3 has a broad tissue expression profile that is distinct from those of Vav and Vav2. Two species of Vav3 transcripts, 3.4 and 5.4 kb, were detected with a differential expression pattern in various tissues. Transient expression of Vav in 293T and NIH 3T3 cells demonstrated that ligand stimulation of several RPTKs (epidermal growth factor receptor [EGFR], Ros, insulin receptor [IR], and insulin-like growth factor I receptor [IGFR]) led to tyrosine phosphorylation of Vav3 and its association with the receptors as well as their downstream signaling molecules, including Shc, Grb2, phospholipase C (PLC-γ), and phosphatidylinositol 3 kinase. In vitro binding assays using glutathione S -transferase-fusion polypeptides containing the GTPase-binding domains of Rok-α, Pak, or Ack revealed that overexpression of Vav3 in NIH 3T3 cells resulted in the activation of Rac-1 and Cdc42 whereas a deletion mutant lacking the N-terminal calponin homology and acidic region domains activated RhoA and Rac-1 but lost the ability to activate Cdc42. Vav3 induced marked membrane ruffles and microspikes in NIH 3T3 cells, while the N-terminal truncation mutants of Vav3 significantly enhanced membrane ruffle formation but had a reduced ability to induce microspikes. Activation of IR further enhanced the ability of Vav3 to induce membrane ruffles, but IGFR activation specifically promoted Vav3-mediated microspike formation. N-terminal truncation of Vav3 activated its transforming potential, as measured by focus-formation assays. We conclude that Vav3 mediates RPTK signaling and regulates GTPase activity, its native and mutant forms are able to modulate cell morphology, and it has the potential to induce cell transformation." @default.
- W2154683723 created "2016-06-24" @default.
- W2154683723 creator A5009760367 @default.
- W2154683723 creator A5020997600 @default.
- W2154683723 creator A5033801009 @default.
- W2154683723 creator A5043891387 @default.
- W2154683723 creator A5071641414 @default.
- W2154683723 creator A5081882500 @default.
- W2154683723 creator A5083233960 @default.
- W2154683723 creator A5091501023 @default.
- W2154683723 date "2000-12-01" @default.
- W2154683723 modified "2023-10-18" @default.
- W2154683723 title "Vav3 Mediates Receptor Protein Tyrosine Kinase Signaling, Regulates GTPase Activity, Modulates Cell Morphology, and Induces Cell Transformation" @default.
- W2154683723 cites W135518686 @default.
- W2154683723 cites W1487500734 @default.
- W2154683723 cites W1527673674 @default.
- W2154683723 cites W1595934817 @default.
- W2154683723 cites W1965518306 @default.
- W2154683723 cites W1972234127 @default.
- W2154683723 cites W1973706463 @default.
- W2154683723 cites W1973782344 @default.
- W2154683723 cites W1979542208 @default.
- W2154683723 cites W1981628302 @default.
- W2154683723 cites W1984592013 @default.
- W2154683723 cites W1984967137 @default.
- W2154683723 cites W1987202628 @default.
- W2154683723 cites W1987989903 @default.
- W2154683723 cites W2001234795 @default.
- W2154683723 cites W2002411373 @default.
- W2154683723 cites W2003976708 @default.
- W2154683723 cites W2007298022 @default.
- W2154683723 cites W2008217531 @default.
- W2154683723 cites W2013592169 @default.
- W2154683723 cites W2023761542 @default.
- W2154683723 cites W2036033286 @default.
- W2154683723 cites W2044356299 @default.
- W2154683723 cites W2044374752 @default.
- W2154683723 cites W2050519522 @default.
- W2154683723 cites W2061913305 @default.
- W2154683723 cites W2070066745 @default.
- W2154683723 cites W2072152826 @default.
- W2154683723 cites W2074885149 @default.
- W2154683723 cites W2075025406 @default.
- W2154683723 cites W2077792958 @default.
- W2154683723 cites W2078475797 @default.
- W2154683723 cites W2079138949 @default.
- W2154683723 cites W2080590768 @default.
- W2154683723 cites W2084759193 @default.
- W2154683723 cites W2087025778 @default.
- W2154683723 cites W2087159097 @default.
- W2154683723 cites W2088877635 @default.
- W2154683723 cites W2090171844 @default.
- W2154683723 cites W2096791952 @default.
- W2154683723 cites W2102787965 @default.
- W2154683723 cites W2104069123 @default.
- W2154683723 cites W2109452714 @default.
- W2154683723 cites W2109974996 @default.
- W2154683723 cites W2126749556 @default.
- W2154683723 cites W2141542738 @default.
- W2154683723 cites W2142529876 @default.
- W2154683723 cites W2142946131 @default.
- W2154683723 cites W2144026996 @default.
- W2154683723 cites W2144111358 @default.
- W2154683723 cites W2154841963 @default.
- W2154683723 cites W2165083476 @default.
- W2154683723 cites W2168635603 @default.
- W2154683723 cites W2326153836 @default.
- W2154683723 doi "https://doi.org/10.1128/mcb.20.24.9212-9224.2000" @default.
- W2154683723 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/102179" @default.
- W2154683723 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11094073" @default.
- W2154683723 hasPublicationYear "2000" @default.
- W2154683723 type Work @default.
- W2154683723 sameAs 2154683723 @default.
- W2154683723 citedByCount "138" @default.
- W2154683723 countsByYear W21546837232012 @default.
- W2154683723 countsByYear W21546837232013 @default.
- W2154683723 countsByYear W21546837232014 @default.
- W2154683723 countsByYear W21546837232015 @default.
- W2154683723 countsByYear W21546837232016 @default.
- W2154683723 countsByYear W21546837232017 @default.
- W2154683723 countsByYear W21546837232018 @default.
- W2154683723 countsByYear W21546837232019 @default.
- W2154683723 countsByYear W21546837232020 @default.
- W2154683723 countsByYear W21546837232021 @default.
- W2154683723 countsByYear W21546837232022 @default.
- W2154683723 countsByYear W21546837232023 @default.
- W2154683723 crossrefType "journal-article" @default.
- W2154683723 hasAuthorship W2154683723A5009760367 @default.
- W2154683723 hasAuthorship W2154683723A5020997600 @default.
- W2154683723 hasAuthorship W2154683723A5033801009 @default.
- W2154683723 hasAuthorship W2154683723A5043891387 @default.
- W2154683723 hasAuthorship W2154683723A5071641414 @default.
- W2154683723 hasAuthorship W2154683723A5081882500 @default.
- W2154683723 hasAuthorship W2154683723A5083233960 @default.
- W2154683723 hasAuthorship W2154683723A5091501023 @default.
- W2154683723 hasBestOaLocation W21546837232 @default.
- W2154683723 hasConcept C101544691 @default.
- W2154683723 hasConcept C104317684 @default.