Drosophila dSmad2 and Atr‐I transmit activin/TGFβ signals

Much is known about the three subfamilies of the TGFβ superfamily in vertebrates—the TGFβs, dpp/BMPs, and activins. Signalling in each subfamily is dependent on both shared and unique cell surface receptors and Smads. In invertebrates, mutants for BMP pathway components have been extensively characterized, but thus far, evidence for an activin‐ or TGFβ‐like pathway has been lacking, preventing the use of the extensive genetic tools available for studying several key issues of TGFβ signalling.

[1]  J. Massagué,et al.  Responsiveness to Transforming Growth Factor-@ (TGF-@) Restored by Genetic Complementation between Cells Defective in TGF-P Receptors I and 11” , 2001 .

[2]  八木 健,et al.  Alternatively spliced variant of smad2 lacking exon 3 : comparison with wild-type smad2 and smad3 , 2001 .

[3]  M. O’Connor,et al.  Synergistic signaling by two BMP ligands through the SAX and TKV receptors controls wing growth and patterning in Drosophila. , 1998, Development.

[4]  Yigong Shi,et al.  Crystal Structure of a Smad MH1 Domain Bound to DNA Insights on DNA Binding in TGF-β Signaling , 1998, Cell.

[5]  K. Miyazono,et al.  Interplay of signal mediators of decapentaplegic (Dpp): molecular characterization of mothers against dpp, Medea, and daughters against dpp. , 1998, Molecular biology of the cell.

[6]  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.

[7]  Takeshi Imamura,et al.  Smad proteins exist as monomers in vivo and undergo homo‐ and hetero‐oligomerization upon activation by serine/threonine kinase receptors , 1998, The EMBO journal.

[8]  Denis Vivien,et al.  Direct binding of Smad3 and Smad4 to critical TGFβ‐inducible elements in the promoter of human plasminogen activator inhibitor‐type 1 gene , 1998, The EMBO journal.

[9]  G. Kutty,et al.  Identification of a new member of transforming growth factor-beta superfamily in Drosophila: the first invertebrate activin gene. , 1998, Biochemical and biophysical research communications.

[10]  R. W. Padgett,et al.  TGF‐β signaling, Smads, and tumor suppressors , 1998 .

[11]  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.

[12]  K. Miyazono,et al.  Interaction of Drosophila Inhibitors of Apoptosis with Thick Veins, a Type I Serine/Threonine Kinase Receptor for Decapentaplegic* , 1998, The Journal of Biological Chemistry.

[13]  L. Dobens,et al.  Medea is a Drosophila Smad4 homolog that is differentially required to potentiate DPP responses. , 1998, Development.

[14]  J. Hudson,et al.  The Drosophila Medea gene is required downstream of dpp and encodes a functional homolog of human Smad4. , 1998, Development.

[15]  R. W. Padgett,et al.  The Drosophila gene Medea demonstrates the requirement for different classes of Smads in dpp signaling. , 1998, Development.

[16]  Yigong Shi,et al.  The L3 loop: a structural motif determining specific interactions between SMAD proteins and TGF‐β receptors , 1998, The EMBO journal.

[17]  T. Yoneda,et al.  Smad5 and DPC4 Are Key Molecules in Mediating BMP-2-induced Osteoblastic Differentiation of the Pluripotent Mesenchymal Precursor Cell Line C2C12* , 1998, The Journal of Biological Chemistry.

[18]  Kohei Miyazono,et al.  TGF-β signalling from cell membrane to nucleus through SMAD proteins , 1997, Nature.

[19]  W. Vale,et al.  Smad8 mediates the signaling of the receptor serine kinase , 1997 .

[20]  Ken W. Y. Cho,et al.  Production of a DPP Activity Gradient in the Early Drosophila Embryo through the Opposing Actions of the SOG and TLD Proteins , 1997, Cell.

[21]  K. Miyazono,et al.  Smad6 inhibits signalling by the TGF-β superfamily , 1997, Nature.

[22]  R. W. Padgett,et al.  Drosophila MAD, a member of the Smad family, translocates to the nucleus upon stimulation of the dpp pathway. , 1997, Biochemical and biophysical research communications.

[23]  Takeshi Imamura,et al.  TGF‐β receptor‐mediated signalling through Smad2, Smad3 and Smad4 , 1997 .

[24]  W. Gelbart,et al.  Mothers against dpp participates in a DDP/TGF-beta responsive serine-threonine kinase signal transduction cascade. , 1997, Development.

[25]  J. Baker,et al.  From receptor to nucleus: the Smad pathway. , 1997, Current opinion in genetics & development.

[26]  M. Sekiguchi Genes to cells: edited by Jun-ichi Tomizawa, Blackwell Science Ltd. Institutional: £218.00 (Europe), £242.00 (Rest of World), US$382.00 (USA and Canada). Individual: £65.00 (Europe), £72.00 (Rest of World), US$114.00 (USA and Canada) ISSN 1356 9597 , 1997 .

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

[28]  Nihon Hassei Seibutsu Gakkai,et al.  Genes to cells , 1996 .

[29]  P. Hoodless,et al.  MADR2 Is a Substrate of the TGFβ Receptor and Its Phosphorylation Is Required for Nuclear Accumulation and Signaling , 1996, Cell.

[30]  K. Miyazono,et al.  Phosphorylation of Ser165 in TGF‐beta type I receptor modulates TGF‐beta1‐induced cellular responses. , 1996 .

[31]  J. Baker,et al.  A novel mesoderm inducer, Madr2, functions in the activin signal transduction pathway. , 1996, Genes & development.

[32]  P. Hoodless,et al.  MADR1, a MAD-Related Protein That Functions in BMP2 Signaling Pathways , 1996, Cell.

[33]  K. Miyazono,et al.  Phosphorylation of Ser165 in TGF‐β type I receptor modulates TGF‐β1‐induced cellular responses , 1996, The EMBO journal.

[34]  R. W. Padgett,et al.  The tolkin gene is a tolloid/BMP-1 homologue that is essential for Drosophila development. , 1995, Genetics.

[35]  J. Massagué,et al.  GS domain mutations that constitutively activate T beta R‐I, the downstream signaling component in the TGF‐beta receptor complex. , 1995, The EMBO journal.

[36]  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.

[37]  J. Sekelsky,et al.  Genetic characterization and cloning of mothers against dpp, a gene required for decapentaplegic function in Drosophila melanogaster. , 1995, Genetics.

[38]  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.

[39]  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.

[40]  S. Kunes,et al.  Pattern formation in the visual centers of the Drosophila brain: wingless acts via decapentaplegic to specify the dorsoventral axis , 1994, Cell.

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

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

[43]  R. W. Padgett,et al.  Mutational analysis of the Drosophila tolloid gene, a human BMP-1 homolog. , 1994, Development.

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

[45]  J. Massagué,et al.  Two distinct transmembrane serine/threonine kinases from Drosophila melanogaster form an activin receptor complex , 1994, Molecular and cellular biology.

[46]  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.

[47]  M. O’Connor,et al.  The Drosophila dorsal-ventral patterning gene tolloid is related to human bone morphogenetic protein 1 , 1991, Cell.

[48]  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.

[49]  J. Massagué,et al.  Responsiveness to transforming growth factor-beta (TGF-beta) restored by genetic complementation between cells defective in TGF-beta receptors I and II. , 1991, The Journal of biological chemistry.

[50]  W. Gelbart,et al.  An extensive 3' cis-regulatory region directs the imaginal disk expression of decapentaplegic, a member of the TGF-beta family in Drosophila. , 1991, Development.

[51]  S. Selleck,et al.  The influence of retinal innervation on neurogenesis in the first optic ganglion of drosophila , 1991, Neuron.

[52]  W. Gelbart,et al.  A transcript from a Drosophila pattern gene predicts a protein homologous to the transforming growth factor-β family , 1987, Nature.

[53]  L. Kauvar,et al.  The engrailed locus of drosophila: Structural analysis of an embryonic transcript , 1985, Cell.