Literature DB >> 8119899

Identification of an insulin response element in the fatty acid synthase promoter.

N Moustaïd1, R S Beyer, H S Sul.   

Abstract

We have previously reported that insulin increases fatty acid synthase (FAS) gene transcription, and that sequences responsible for positive regulation are located within the first 332 base pairs of the FAS promoter. To define minimal sequences required for insulin regulation within this region, chimeric constructs containing serial 5' deletions starting at -318 and extending through position +67 of the rat FAS gene ligated to the luciferase reporter gene were transfected into 3T3-L1 adipocytes. Insulin treatment at 10 nM increased luciferase activity 2-3-fold in 3T3-L1 adipocytes transfected with constructs containing progressive deletions from -318 to -67. This stimulation of the FAS promoter activity by insulin was dose-dependent. However, no effect of insulin was observed when fusion constructs containing FAS promoter sequences spanning from -25 or from -19 to +67 were transfected into adipocytes. These results suggest that the insulin response sequences of the FAS gene may be located in the region from -67 to -25. DNase I footprinting using liver nuclear extracts revealed a protected region spanning -71 and -50 in addition to a region near the putative TATA box. Gel mobility shift assays using the sequence from -71 to -50 as a probe revealed nuclear factor(s) from mouse liver and 3T3-L1 adipocytes that specifically complexed with this sequence. Mutational analysis of this region showed that sequences between -68 and -60 are essential for recognition and interaction with a trans-acting factor(s). Moreover, when three tandem repeats of the sequences spanning -68 to -52 were linked to the SV40 promoter and used for transfection, luciferase activity increased 3.6-fold in response to insulin treatment. Thus, we have identified novel cis-acting DNA sequences responsible for insulin regulation of the FAS gene, which interact with nuclear protein(s) from liver and adipocytes and which are found to share limited homology to insulin response sequences present in other genes.

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Year:  1994        PMID: 8119899

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  25 in total

Review 1.  New perspectives in the regulation of hepatic glycolytic and lipogenic genes by insulin and glucose: a role for the transcription factor sterol regulatory element binding protein-1c.

Authors:  Fabienne Foufelle; Pascal Ferré
Journal:  Biochem J       Date:  2002-09-01       Impact factor: 3.857

2.  Transcriptional regulation of the rat fatty acid synthase gene: identification and functional analysis of positive and negative effectors of basal transcription.

Authors:  B Oskouian; V S Rangan; S Smith
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

Review 3.  Fatty acid synthase and liver triglyceride metabolism: housekeeper or messenger?

Authors:  Anne P L Jensen-Urstad; Clay F Semenkovich
Journal:  Biochim Biophys Acta       Date:  2011-10-08

4.  Identification of thyroid hormone response elements in the human fatty acid synthase promoter.

Authors:  S Xiong; S S Chirala; M H Hsu; S J Wakil
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

5.  Identification of upstream stimulatory factor as transcriptional activator of the liver promoter of the glucokinase gene.

Authors:  P B Iynedjian
Journal:  Biochem J       Date:  1998-08-01       Impact factor: 3.857

Review 6.  Synthesis of fat in response to alterations in diet: insights from new stable isotope methodologies.

Authors:  M K Hellerstein
Journal:  Lipids       Date:  1996-03       Impact factor: 1.880

7.  Somatotropin-dependent decrease in fatty acid synthase mRNA abundance in 3T3-F442A adipocytes is the result of a decrease in both gene transcription and mRNA stability.

Authors:  D Yin; S D Clarke; J L Peters; T D Etherton
Journal:  Biochem J       Date:  1998-05-01       Impact factor: 3.857

8.  CREB activation induces adipogenesis in 3T3-L1 cells.

Authors:  J E Reusch; L A Colton; D J Klemm
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

9.  ADD1/SREBP-1c is required in the activation of hepatic lipogenic gene expression by glucose.

Authors:  M Foretz; C Pacot; I Dugail; P Lemarchand; C Guichard; X Le Lièpvre; C Berthelier-Lubrano; B Spiegelman; J B Kim; P Ferré; F Foufelle
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

10.  Human fatty acid synthesis is stimulated by a eucaloric low fat, high carbohydrate diet.

Authors:  L C Hudgins; M Hellerstein; C Seidman; R Neese; J Diakun; J Hirsch
Journal:  J Clin Invest       Date:  1996-05-01       Impact factor: 14.808

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