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PMID: 9409665 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cellular interpretation of multiple TGF-beta signals: intracellular antagonism between activin/BVg1 and BMP-2/4 signaling mediated by Smads.

Development (Cambridge, England) ·Vol. 124 ·No. 22 ·1997-11-00 ·Pages 4467-80

Candia AF, Watabe T, Hawley SH, Onichtchouk D, Zhang Y, Derynck R, Niehrs C, Cho KW

Abstract

During early embryogenesis of Xenopus, dorsoventral polarity of the mesoderm is established by dorsalizing and ventralizing agents, which are presumably mediated by the activity of an activin/BVg1-like protein and Bone Morphogenetic Proteins (BMP), respectively. Interestingly, these two TGF-beta subfamilies are found in overlapping regions during mesoderm patterning. This raises the question of how the presumptive mesodermal cells recognize the multiple TGF-beta signals and differentially interpret this information to assign a particular cell fate. In this study, we have exploited the well characterized model of Xenopus mesoderm induction to determine the intracellular interactions between BMP-2/4 and activin/BVg1 signaling cascades. Using a constitutively active BMP-2/4 receptor that transduces BMP-2/4 signals in a ligand-independent fashion, we demonstrate that signals provided by activin/BVg1 and BMP modulate each other's activity and that this crosstalk occurs through intracellular mechanisms. In assays using BMP-2/4 and activin/BVg1-specific reporters, we determined that the specificity of BMP-2/4 and activin/BVg1 signaling is mediated by Smad1 and Smad2, respectively. These Smads should be considered as the mediators of the intracellular antagonism between BMP-2/4 and activin/BVg1 signaling possibly through sequestration of a limited pool of Smad4. Consistent with such a mechanism, Smad4 interacts functionally with both Smad1 and -2 to potentiate their signaling activities, and a dominant negative variant of Smad4 can inhibit both activin/BVg1 and BMP-2/4 mediated signaling Finally, we demonstrate that an activin/BVg1-dependent transcriptional complex contains both Smad2 and Smad4 and thereby provides a physical basis for the functional involvement of both Smads in TGF-beta-dependent transcriptional regulation. Thus, Smad4 plays a central role in synergistically activating activin/BVg1 and BMP-dependent transcription and functions as an intracellular sensor for TGF-beta-related signals.

MeSH Terms
Activins Animals Base Sequence Bone Morphogenetic Protein 2 Bone Morphogenetic Protein 4 Bone Morphogenetic Protein Receptors Bone Morphogenetic Proteins/metabolism DNA Primers/genetics DNA-Binding Proteins/genetics,metabolism Female Goosecoid Protein Homeodomain Proteins Inhibins/metabolism Intracellular Fluid/metabolism Male Nerve Growth Factors Polymerase Chain Reaction Promoter Regions, Genetic Receptors, Cell Surface/genetics,metabolism Receptors, Growth Factor Repressor Proteins Signal Transduction Smad Proteins Smad2 Protein Smad4 Protein Trans-Activators/metabolism Transcription Factors Transforming Growth Factor beta/metabolism Xenopus/embryology,genetics,metabolism Xenopus Proteins
Chemicals
Bone Morphogenetic Protein 2 Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins DNA Primers DNA-Binding Proteins Goosecoid Protein Homeodomain Proteins MXD1 protein, Xenopus Nerve Growth Factors Receptors, Cell Surface Receptors, Growth Factor Repressor Proteins Smad Proteins Smad2 Protein Smad2 protein, Xenopus Smad4 Protein Trans-Activators Transcription Factors Transforming Growth Factor beta Xenopus Proteins bmp4 protein, Xenopus smad4.1 protein, Xenopus smad4.2 protein, Xenopus Activins Inhibins Bone Morphogenetic Protein Receptors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Candia A F
Department of Developmental and Cell Biology, and Developmental Biology Center, University of California at Irvine, 92717-2300, USA.
Watabe T
Hawley S H
Onichtchouk D
Zhang Y
Derynck R
Niehrs C
Cho K W
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1997-11-00
Pages
4467-80
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NCI NIH HHS · CA63101 · United States
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