Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/182497
Title: The hepatocyte nuclear factor 4 (HNF-4) represses the mitochondrial HMG-CoA synthase gene
Author: Rodríguez Rubio, Joan Carles
Ortiz, José A.
García Hegardt, Fausto
Haro Bautista, Diego
Keywords: Àcids grassos
Mitocondris
Regulació del metabolisme
Fatty acids
Mitochondria
Metabolic regulation
Issue Date: 1998
Publisher: Elsevier B.V.
Abstract: We have recently shown that the gene for the mitochondrial HMG-CoA synthase is a target for PPAR and that this receptor mediates the induction of this gene by fatty acids. With the aim of gaining further insight into the function and regulation of this gene we examined the effect of other members of the nuclear hormone receptor superfamily on its expression. We previously identified a regulatory element in the mitochondrial HMG-CoA synthase gene promoter that confers transcriptional regulation by PPAR, RXR and the orphan nuclear receptor COUP-TF, In this study we demonstrate a trans-repressing regulatory function for HNF-4 at this same nuclear receptor response element (NRRE). HNF-4 binds to the mitochondrial HMG-CoA synthase NRRE, and, in cotransfection assays in HepG2 cells, it represses PPAR-dependent activation of a reporter gene linked to the mitochondrial HMG-CoA synthase gene promoter. These results suggest that the mitochondrial HMG-CoA synthase gene is subject to differential regulation by the interplay of multiple members of the nuclear hormone receptor superfamily.
Note: Versió postprint del document publicat a: https://www.sciencedirect.com/science/article/abs/pii/S0006291X97980323?via%3Dihub
It is part of: Biochemical and Biophysical Research Communications, 1998, vol. 242, num. 3, p. 692-696
URI: http://hdl.handle.net/2445/182497
ISSN: 0006-291X
Appears in Collections:Articles publicats en revistes (Bioquímica i Fisiologia)

Files in This Item:
File Description SizeFormat 
570946.pdf696.31 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.