Scaffold attachment factor B1 directly interacts with nuclear receptors in living cells and represses transcriptional activity.

Détails

ID Serval
serval:BIB_A9BFC6B17C5E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Scaffold attachment factor B1 directly interacts with nuclear receptors in living cells and represses transcriptional activity.
Périodique
Journal of Molecular Endocrinology
Auteur⸱e⸱s
Debril M.B., Dubuquoy L., Feige J.N., Wahli W., Desvergne B., Auwerx J., Gelman L.
ISSN
0952-5041[print], 0952-5041[linking]
Statut éditorial
Publié
Date de publication
2005
Peer-reviewed
Oui
Volume
35
Numéro
3
Pages
503-517
Langue
anglais
Notes
Publication types: In Vitro ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Transcriptional activity relies on coregulators that modify the chromatin structure and serve as bridging factors between transcription factors and the basal transcription machinery. Using the DE domain of human peroxisome proliferator-activated receptor gamma (PPARgamma) as bait in a yeast two-hybrid screen of a human adipose tissue library, we isolated the scaffold attachment factor B1 (SAFB1/HET/HAP), which was previously shown to be a corepressor of estrogen receptor alpha. We show here that SAFB1 has a very broad tissue expression profile in human and is also expressed all along mouse embryogenesis. SAFB1 interacts in pull-down assays not only with PPARgamma but also with all nuclear receptors tested so far, albeit with different affinities. The association of SAFB1 and PPARgamma in vivo is further demonstrated by fluorescence resonance energy transfer (FRET) experiments in living cells. We finally show that SAFB1 is a rather general corepressor for nuclear receptors. Its change in expression during the early phases of adipocyte and enterocyte differentiation suggests that SAFB1 potentially influences cell proliferation and differentiation decisions.
Mots-clé
Adipocytes/metabolism, Animals, Base Sequence, COS Cells, Cell Line, Cercopithecus aethiops, DNA, Complementary/genetics, Embryonic Development/genetics, Female, Humans, Male, Matrix Attachment Region Binding Proteins/genetics, Matrix Attachment Region Binding Proteins/metabolism, Mice, Nuclear Matrix-Associated Proteins/genetics, Nuclear Matrix-Associated Proteins/metabolism, PPAR gamma/metabolism, Pregnancy, Receptors, Cytoplasmic and Nuclear/metabolism, Receptors, Estrogen/genetics, Receptors, Estrogen/metabolism, Recombinant Proteins/genetics, Recombinant Proteins/metabolism, Repressor Proteins/genetics, Repressor Proteins/metabolism, Tissue Distribution, Transcription, Genetic, Two-Hybrid System Techniques
Pubmed
Web of science
Création de la notice
24/01/2008 15:26
Dernière modification de la notice
20/08/2019 15:13
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