Transforming growth factor beta enhances the glucocorticoid response of the mouse mammary tumor virus promoter through Smad and GA-binding proteins

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Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_26E25847FBF9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Transforming growth factor beta enhances the glucocorticoid response of the mouse mammary tumor virus promoter through Smad and GA-binding proteins
Périodique
Journal of Virology
Auteur⸱e⸱s
Aurrekoetxea-Hernandez K., Buetti E.
ISSN
0022-538X (Print)
Statut éditorial
Publié
Date de publication
03/2004
Volume
78
Numéro
5
Pages
2201-11
Notes
Journal Article Research Support, Non-U.S. Gov't --- Old month value: Mar
Résumé
Tissue-specific transcription is advantageously investigated by using viral promoters, which are selected for compact regulatory elements. Mouse mammary tumor virus (MMTV) has adapted to specialized cell types and targets initially B lymphocytes. We previously showed that, in B-cell lines, glucocorticoid-induced MMTV transcription requires an ETS family factor, GA-binding protein (GABP), bound in tandem to the MMTV DNA next to the glucocorticoid receptor (GR). We now report that transforming growth factor beta (TGF-beta) superinduces this response up to 10-fold through binding of its effectors, Smads, between the GABP-binding motifs. The basal level was unaffected. The TGF-beta-glucocorticoid cooperation also depended on GR and GABP binding, was transferable to another promoter, and occurred both with transiently transfected and with integrated templates. Smad3 associated in vitro with GR, with GABPalpha (via the MH2 domain), and with GABPbeta, Smad4 only with GABPalpha. Interactions of Smad3 with GABP (when coexpressed or endogenous to B cells) were shown by coprecipitation and by mammalian two-hybrid assay. This composite DNA element integrates three signaling pathways deriving from TGF-beta, glucocorticoid hormones, and a unique ETS factor, and may allow MMTV to exploit factors from the milk. It may as well indicate novel possibilities for cellular regulatory networks.
Mots-clé
Animals Base Sequence COS Cells Cell Line, Tumor DNA-Binding Proteins/*metabolism GA-Binding Protein Transcription Factor Gene Expression Regulation/*drug effects Glucocorticoids/*pharmacology Mammary Tumor Virus, Mouse/*genetics Mice Promoter Regions (Genetics)/*genetics Protein Binding Receptors, Glucocorticoid/metabolism Response Elements/genetics Smad3 Protein Smad4 Protein Terminal Repeat Sequences/genetics Trans-Activators/*metabolism Transcription Factors/*metabolism Transforming Growth Factor beta/*pharmacology
Pubmed
Web of science
Open Access
Oui
Création de la notice
25/01/2008 14:25
Dernière modification de la notice
20/08/2019 13:05
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