Synergistic signaling by two BMP ligands through the SAX and TKV receptors controls wing growth and patterning in Drosophila.

In Drosophila wing discs, a morphogen gradient of DPP has been proposed to determine the transcriptional response thresholds of the downstream genes sal and omb. We present evidence that the concentration of the type I receptor TKV must be low to allow long-range DPP diffusion. Low TKV receptor concentrations result, however, in low signaling activity. To enhance signaling at low DPP concentrations, we find that a second ligand, GBB, augments DPP/TKV activity. GBB signals primarily through the type I receptor SAX, which synergistically enhances TKV signaling and is required for proper OMB expression. We show that OMB expression in wing discs requires synergistic signaling by multiple ligands and receptors to overcome the limitations imposed on DPP morphogen function by receptor concentration levels.

[1]  S. Torres-Schumann,et al.  TGF-beta/BMP superfamily members, Gbb-60A and Dpp, cooperate to provide pattern information and establish cell identity in the Drosophila wing. , 1998, Development.

[2]  F. Hoffmann,et al.  A genetic screen for modifiers of Drosophila decapentaplegic signaling identifies mutations in punt, Mothers against dpp and the BMP-7 homologue, 60A. , 1998, Development.

[3]  S. Selleck,et al.  dally, a Drosophila glypican, controls cellular responses to the TGF-beta-related morphogen, Dpp. , 1997, Development.

[4]  Minoru Watanabe,et al.  Smad4 and FAST-1 in the assembly of activin-responsive factor , 1997, Nature.

[5]  J. Massagué,et al.  Distinct roles of type I bone morphogenetic protein receptors in the formation and differentiation of cartilage. , 1997, Genes & development.

[6]  J. Marsh,et al.  Defects in glucuronate biosynthesis disrupt Wingless signaling in Drosophila. , 1997, Development.

[7]  S. Cohen,et al.  Problems and paradigms: Morphogens and pattern formation , 1997 .

[8]  Kirby D. Johnson,et al.  Drosophila Mad binds to DNA and directly mediates activation of vestigial by Decapentaplegic , 1997, Nature.

[9]  A. Hata,et al.  TGF-β signalling through the Smad pathway , 1997 .

[10]  J. Massagué,et al.  The TGF-beta family mediator Smad1 is phosphorylated directly and activated functionally by the BMP receptor kinase. , 1997, Genes & development.

[11]  A. Fainsod,et al.  The dorsalizing and neural inducing gene follistatin is an antagonist of BMP-4 , 1997, Mechanisms of Development.

[12]  K. Miyazono,et al.  TGF-beta signalling from cell membrane to nucleus through SMAD proteins. , 1997, Nature.

[13]  S Cohen,et al.  Morphogens and pattern formation. , 1997, BioEssays : news and reviews in molecular, cellular and developmental biology.

[14]  J. D. de Celis Expression and function of decapentaplegic and thick veins during the differentiation of the veins in the Drosophila wing. , 1997, Development.

[15]  E. Marin,et al.  The spalt gene links the A/P compartment boundary to a linear adult structure in the Drosophila wing. , 1997, Development.

[16]  W. Gelbart,et al.  Signaling through both type I DPP receptors is required for anterior-posterior patterning of the entire Drosophila wing. , 1997, Development.

[17]  G. Struhl,et al.  Dual Roles for Patched in Sequestering and Transducing Hedgehog , 1996, Cell.

[18]  R. Derynck,et al.  Receptor-associated Mad homologues synergize as effectors of the TGF-β response , 1996, Nature.

[19]  Y. Sasai,et al.  Dorsoventral Patterning in Xenopus: Inhibition of Ventral Signals by Direct Binding of Chordin to BMP-4 , 1996, Cell.

[20]  B. Hogan,et al.  Bone morphogenetic proteins: multifunctional regulators of vertebrate development. , 1996, Genes & development.

[21]  Manuel Calleja,et al.  Two distinct mechanisms for long-range patterning by Decapentaplegic in the Drosophila wing , 1996, Nature.

[22]  K. Basler,et al.  Dpp receptors are autonomously required for cell proliferation in the entire developing Drosophila wing. , 1996, Development.

[23]  R. Barrio,et al.  A gene complex acting downstream of dpp in Drosophila wing morphogenesis , 1996, Nature.

[24]  G. Struhl,et al.  Direct and Long-Range Action of a DPP Morphogen Gradient , 1996, Cell.

[25]  G. Pflugfelder,et al.  Control of the Gene optomotor-blind in Drosophila Wing Development by decapentaplegic and wingless , 1996, Science.

[26]  J. Massagué,et al.  Human type II receptor for bone morphogenic proteins (BMPs): extension of the two-kinase receptor model to the BMPs , 1995, Molecular and cellular biology.

[27]  M. Affolter,et al.  An absolute requirement for both the type II and type I receptors, punt and thick veins, for Dpp signaling in vivo , 1995, Cell.

[28]  W. Gelbart,et al.  Drosophila Dpp signaling is mediated by the punt gene product: A dual ligand-binding type II receptor of the TGFβ receptor family , 1995, Cell.

[29]  M. O’Connor,et al.  Characterization of tolloid-related-1: a BMP-1-like product that is required during larval and pupal stages of Drosophila development. , 1994, Developmental biology.

[30]  M. Levine,et al.  The screw gene encodes a ubiquitously expressed member of the TGF-beta family required for specification of dorsal cell fates in the Drosophila embryo. , 1994, Genes & development.

[31]  D. Kimelman,et al.  Combinatorial signaling in development. , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[32]  W. Gelbart,et al.  Characterization and relationship of dpp receptors encoded by the saxophone and thick veins genes in Drosophila , 1994, Cell.

[33]  J. Massagué,et al.  Identification of two bone morphogenetic protein type I receptors in Drosophila and evidence that Brk25D is a decapentaplegic receptor , 1994, Cell.

[34]  Markus Affolter,et al.  Receptor serine/threonine kinases implicated in the control of Drosophila body pattern by decapentaplegic , 1994, Cell.

[35]  R. W. Padgett,et al.  The Drosophila saxophone gene: a serine-threonine kinase receptor of the TGF-beta superfamily. , 1994, Science.

[36]  D. Kingsley,et al.  The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms. , 1994, Genes & development.

[37]  N. Perrimon,et al.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. , 1993, Development.

[38]  G. Struhl,et al.  The torso receptor localizes as well as transduces the spatial signal specifying terminal body pattern in Drosophila , 1993, Nature.

[39]  W. Gelbart,et al.  An activity gradient of decapentaplegic is necessary for the specification of dorsal pattern elements in the Drosophila embryo. , 1993, Development.

[40]  K. Anderson,et al.  decapentaplegic acts as a morphogen to organize dorsal-ventral pattern in the Drosophila embryo , 1992, Cell.

[41]  F. Hoffmann,et al.  Sequence, biochemical characterization, and developmental expression of a new member of the TGF-beta superfamily in Drosophila melanogaster. , 1992, Developmental biology.

[42]  W. Gelbart,et al.  Drosophila 60A gene, another transforming growth factor beta family member, is closely related to human bone morphogenetic proteins. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[43]  W. Gelbart The decapentaplegic gene: a TGF-beta homologue controlling pattern formation in Drosophila. , 1989, Development.