• Nature · Sep 1999

    Silencing of TGF-beta signalling by the pseudoreceptor BAMBI.

    • D Onichtchouk, Y G Chen, R Dosch, V Gawantka, H Delius, J Massagué, and C Niehrs.
    • Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
    • Nature. 1999 Sep 30; 401 (6752): 480-5.

    AbstractMembers of the transforming growth factor-beta (TGF-beta) superfamily, including TGF-beta, bone morphogenetic proteins (BMPs), activins and nodals, are vital for regulating growth and differentiation. These growth factors transduce their signals through pairs of transmembrane type I and type II receptor kinases. Here, we have cloned a transmembrane protein, BAMBI, which is related to TGF-beta-family type I receptors but lacks an intracellular kinase domain. We show that BAMBI is co-expressed with the ventralizing morphogen BMP4 (refs 5, 6) during Xenopus embryogenesis and that it requires BMP signalling for its expression. The protein stably associates with TGF-beta-family receptors and inhibits BMP and activin as well as TGF-beta signalling. Finally, we provide evidence that BAMBI's inhibitory effects are mediated by its intracellular domain, which resembles the homodimerization interface of a type I receptor and prevents the formation of receptor complexes. The results indicate that BAMBI negatively regulates TGF-beta-family signalling by a regulatory mechanism involving the interaction of signalling receptors with a pseudoreceptor.

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