Please use this identifier to cite or link to this item: https://doi.org/10.1074/jbc.M108368200
Title: Sprouty2 inhibits the Ras/MAP kinase pathway by inhibiting the activation of Raf
Authors: Yusoff, P.
Lao, D.-H.
Ong, S.H. 
Miin Wong, E.S.
Lim, J.
Lo, T.L.
Leong, H.F.
Fong, C.W.
Guy, G.R. 
Issue Date: 1-Feb-2002
Citation: Yusoff, P., Lao, D.-H., Ong, S.H., Miin Wong, E.S., Lim, J., Lo, T.L., Leong, H.F., Fong, C.W., Guy, G.R. (2002-02-01). Sprouty2 inhibits the Ras/MAP kinase pathway by inhibiting the activation of Raf. Journal of Biological Chemistry 277 (5) : 3195-3201. ScholarBank@NUS Repository. https://doi.org/10.1074/jbc.M108368200
Abstract: Several genetic studies in Drosophila have shown that the dSprouty (dSpry) protein inhibits the Ras/mitogen-activated protein (MAP) kinase pathway induced by various activated receptor tyrosine kinase receptors, most notably those of the epidermal growth factor receptor (EGFR) and fibroblast growth factor receptor (FGFR). Currently, the mode of action of dSpry is unknown, and the point of inhibition remains controversial. There are at least four mammalian Spry isoforms that have been shown to co-express preferentially with FGFRs as compared with EGFRs. In this study, we investigated the effects of the various mammalian Spry isoforms on the Ras/MAP kinase pathway in cells overexpressing constitutively active FGFR1. hSpry2 was significantly more potent than mSpry1. or mSpry4 in inhibiting the Ras/MAP kinase pathway. Additional experiments indicated that full-length hSpry2 was required for its full potency. hSpry2 had no inhibitory effect on either the JNK or the p38 pathway and displayed no inhibition of FRS2 phosphorylation, Akt activation, and Ras activation. Constitutively active mutants of Ras, Raf, and Mek were employed to locate the prospective point of inhibition of hSpry2 downstream of activated Ras. Results from this study indicated that hSpry2 exerted its inhibitory effect at the level of Raf, which was verified in a Raf activation assay in an FGF signaling context.
Source Title: Journal of Biological Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/112085
ISSN: 00219258
DOI: 10.1074/jbc.M108368200
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