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Brief Communication
Nature Cell Biology  4, 170 - 174 (2002)
Published online: 21 January 2002; | doi:10.1038/ncb750

Sef is a feedback-induced antagonist of Ras/MAPK-mediated FGF signalling

Maximilian Fürthauer, Wei Lin, Siew-Lan Ang, Bernard Thisse & Christine Thisse

Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, BP 163, 67404 Illkirch cedex, CU de Strasbourg, France.

Correspondence should be addressed to Christine Thisse thisse@igbmc.u-strasbg.fr
Fibroblast growth factors (FGFs) are pleiotrophic growth factors that control cell proliferation, migration, differentiation and embryonic patterning1. During early zebrafish embryonic development, FGFs regulate dorsoventral patterning by controlling ventral bone morphogenetic protein (BMP) expression2, 3. FGFs function by binding and activating high-affinity tyrosine kinase receptors4. FGF activity is negatively regulated by members of the Sprouty family, which antagonize Ras signalling induced by receptor tyrosine kinases3, 5, 6, 7, 8. On the basis of similarities in their expression patterns during embryonic development, we have identified five genes that define a synexpression group — fgf8, fgf3, sprouty2, sprouty4, as well as a novel gene, sef (similar expression to fgf genes). Sef encodes a conserved putative transmembrane protein that shares sequence similarities with the intracellular domain of the interleukin 17 receptor9. Here we show that in zebrafish, Sef functions as a feedback-induced antagonist of Ras/Raf/MEK/MAPK-mediated FGF signalling.


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Nature Cell Biology
ISSN: 1465-7392
EISSN: 1476-4679
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