Literature DB >> 7488098

Truncated type II receptor for BMP-4 induces secondary axial structures in Xenopus embryos.

T Ishikawa1, H Yoshioka, H Ohuchi, S Noji, T Nohno.   

Abstract

BRK-3 is a vertebrate type II receptor for BMP-4 distantly related to invertebrate type II receptors for BMP-2/BMP-4/dpp, such as daf-4 and punt. BRK-3 has a long carboxy-terminal sequence following intracellular kinase domain and is capable of forming a high-affinity complex with a type I receptor, BRK-2. To examine the role of BRK-2 + BRK-3 receptor complex in BMP signaling during early embryogenesis, the dominant-negative form of BRK-3 was ectopically expressed in the Xenopus embryos. A secondary body axis expressing the Sonic hedgehog and N-CAM genes is induced by injecting mRNA encoding truncated form of BRK-3 into ventral marginal region, implicating the BMP signaling in axial mesoderm induction. Formation of the secondary axis depends on whether the deletion extends into the kinase domain, not into the carboxy-terminal tail, suggesting that the kinase domain, but not the tail region, is essential for BMP signaling.

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Year:  1995        PMID: 7488098     DOI: 10.1006/bbrc.1995.2587

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  9 in total

Review 1.  Antagonism of activin by activin chimeras.

Authors:  Uwe Muenster; Radhika Korupolu; Ratindra Rastogi; Jessica Read; Wolfgang H Fischer
Journal:  Vitam Horm       Date:  2011       Impact factor: 3.421

2.  A novel regulatory mechanism of the bone morphogenetic protein (BMP) signaling pathway involving the carboxyl-terminal tail domain of BMP type II receptor.

Authors:  Mun Chun Chan; Peter H Nguyen; Brandi N Davis; Nobumichi Ohoka; Hidetoshi Hayashi; Keyong Du; Giorgio Lagna; Akiko Hata
Journal:  Mol Cell Biol       Date:  2007-06-18       Impact factor: 4.272

3.  Functional heterogeneity of bone morphogenetic protein receptor-II mutants found in patients with primary pulmonary hypertension.

Authors:  Ayako Nishihara; Tetsuro Watabe; Takeshi Imamura; Kohei Miyazono
Journal:  Mol Biol Cell       Date:  2002-09       Impact factor: 4.138

Review 4.  The Wnt and BMP families of signaling morphogens at the vertebrate neuromuscular junction.

Authors:  Juan P Henríquez; Catherine E Krull; Nelson Osses
Journal:  Int J Mol Sci       Date:  2011-12-05       Impact factor: 5.923

5.  Bone morphogenetic protein signaling is required for maintenance of differentiated phenotype, control of proliferation, and hypertrophy in chondrocytes.

Authors:  M Enomoto-Iwamoto; M Iwamoto; Y Mukudai; Y Kawakami; T Nohno; Y Higuchi; S Takemoto; H Ohuchi; S Noji; K Kurisu
Journal:  J Cell Biol       Date:  1998-01-26       Impact factor: 10.539

Review 6.  Bone morphogenetic proteins, genetics and the pathophysiology of primary pulmonary hypertension.

Authors:  M De Caestecker; B Meyrick
Journal:  Respir Res       Date:  2001-06-11

Review 7.  Bone morphogenetic protein signaling in vertebrate motor neurons and neuromuscular communication.

Authors:  Nelson Osses; Juan P Henríquez
Journal:  Front Cell Neurosci       Date:  2015-01-27       Impact factor: 5.505

8.  Differential roles for bone morphogenetic protein (BMP) receptor type IB and IA in differentiation and specification of mesenchymal precursor cells to osteoblast and adipocyte lineages.

Authors:  D Chen; X Ji; M A Harris; J Q Feng; G Karsenty; A J Celeste; V Rosen; G R Mundy; S E Harris
Journal:  J Cell Biol       Date:  1998-07-13       Impact factor: 10.539

9.  BMP gradients steer nerve growth cones by a balancing act of LIM kinase and Slingshot phosphatase on ADF/cofilin.

Authors:  Zhexing Wen; Liang Han; James R Bamburg; Sangwoo Shim; Guo-li Ming; James Q Zheng
Journal:  J Cell Biol       Date:  2007-07-02       Impact factor: 10.539

  9 in total

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