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FLRG, an activin-binding protein, is a new target of TGFβ transcription activation through Smad proteins
by
Gadoux, Mylène
, Magaud, Jean-Pierre
, Corbo, Laura
, Martel, Sylvie
, Lamadon, Christine
, Maguer-Satta, Véronique
, Hayette, Sandrine
, Morera, Anne-Marie
, Rimokh, Ruth
, Bartholin, Laurent
, Bertrand, Suzanne
in
Activin
/ activin-binding protein
/ Analysis
/ Binding sites
/ Biological and medical sciences
/ cDNA
/ Electrophoretic mobility
/ Expression vectors
/ FLRG gene
/ Follistatin
/ Fundamental and applied biological sciences. Psychology
/ Gel electrophoresis
/ Gene deletion
/ Gene expression
/ Gene regulation
/ Infection
/ Molecular and cellular biology
/ Peptide hormones
/ Proteins
/ Smad protein
/ Smad3 protein
/ Smad4 protein
/ Sp1 protein
/ Transcription activation
/ Transfection
/ Transforming growth factors
2001
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FLRG, an activin-binding protein, is a new target of TGFβ transcription activation through Smad proteins
by
Gadoux, Mylène
, Magaud, Jean-Pierre
, Corbo, Laura
, Martel, Sylvie
, Lamadon, Christine
, Maguer-Satta, Véronique
, Hayette, Sandrine
, Morera, Anne-Marie
, Rimokh, Ruth
, Bartholin, Laurent
, Bertrand, Suzanne
in
Activin
/ activin-binding protein
/ Analysis
/ Binding sites
/ Biological and medical sciences
/ cDNA
/ Electrophoretic mobility
/ Expression vectors
/ FLRG gene
/ Follistatin
/ Fundamental and applied biological sciences. Psychology
/ Gel electrophoresis
/ Gene deletion
/ Gene expression
/ Gene regulation
/ Infection
/ Molecular and cellular biology
/ Peptide hormones
/ Proteins
/ Smad protein
/ Smad3 protein
/ Smad4 protein
/ Sp1 protein
/ Transcription activation
/ Transfection
/ Transforming growth factors
2001
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FLRG, an activin-binding protein, is a new target of TGFβ transcription activation through Smad proteins
by
Gadoux, Mylène
, Magaud, Jean-Pierre
, Corbo, Laura
, Martel, Sylvie
, Lamadon, Christine
, Maguer-Satta, Véronique
, Hayette, Sandrine
, Morera, Anne-Marie
, Rimokh, Ruth
, Bartholin, Laurent
, Bertrand, Suzanne
in
Activin
/ activin-binding protein
/ Analysis
/ Binding sites
/ Biological and medical sciences
/ cDNA
/ Electrophoretic mobility
/ Expression vectors
/ FLRG gene
/ Follistatin
/ Fundamental and applied biological sciences. Psychology
/ Gel electrophoresis
/ Gene deletion
/ Gene expression
/ Gene regulation
/ Infection
/ Molecular and cellular biology
/ Peptide hormones
/ Proteins
/ Smad protein
/ Smad3 protein
/ Smad4 protein
/ Sp1 protein
/ Transcription activation
/ Transfection
/ Transforming growth factors
2001
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FLRG, an activin-binding protein, is a new target of TGFβ transcription activation through Smad proteins
Journal Article
FLRG, an activin-binding protein, is a new target of TGFβ transcription activation through Smad proteins
2001
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Overview
The FLRG gene encodes a secreted glycoprotein that binds to activin and is highly homologous to follistatin, an activin ligand. We cloned the promoter region of the human FLRG gene, and defined the minimal region necessary for transcription activation in a reporter-system assay. We showed that the fragment between positions −130 and +6, which consists of multiple consensus Sp1-binding sites, is required for the constitutive expression of the FLRG gene. We demonstrate here that FLRG mRNA expression is rapidly induced by TGFβ or by transfection with Smad protein expression vectors in human HepG2 cells. We investigated the transcription-regulation mechanism of FLRG expression in HepG2 cells following treatment with TGFβ. By deletion and point-mutation analysis of the FLRG promoter, we identified a Smad-binding element involved in the TGFβ-inducible expression of the FLRG gene. Moreover, transactivation of the FLRG promoter by TGFβ was compromised by dominant-negative mutants of Smad3 and Smad4 proteins. In addition, gel electrophoresis mobility-shift assays demonstrated the specific interaction of Smad3 and Smad4 proteins with the Smad-binding element consensus motif found in the FLRG promoter. Taken together, our data imply that Smad proteins participate in the regulation of expression of FLRG, a new target of TGFβ transcription activation.
Publisher
Nature Publishing,Nature Publishing Group
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