Literature DB >> 7864828

Analysis of c-fos expression in the butyrate-induced F-98 glioma cell differentiation.

S J Tang1, Y M Huang, F F Wang.   

Abstract

The functional induction of c-fos in the sodium butyrate-induced differentiation of F-98 glioma cells was studied. Fos protein level was increased by butyrate. In contrast, c-Jun protein was constitutively expressed and was not affected by butyrate. Gel-retardation assay indicates Fos as a component of the complex formed between the consensus oligonucleotide of the TPA (PMA, phorbol 12-myristate 13-acetate) response element (TRE) and nuclear extract prepared from butyrate-treated cells. Transfection studies showed that butyrate increased transcription from a multimeric TRE-driven reporter construct, and the effect was mimicked by transfecting cells with fos-expression plasmid. Furthermore, under conditions of c-fos over-expression, transactivation by butyrate was essentially abolished. These data suggest that Fos induction had a functional role in gene activation. Characterization of stable c-fos transfectants demonstrated that these cells displayed alterations in morphology, showed serum-dependent growth, had slower growth rates and grew to lower saturation densities than did untransfected F-98 cells or transfected cells that did not express c-fos. Immunofluorescent staining indicated that fos transfectants also had elevated glial fibrillary acidic protein ('GFAP') expression. Transfection of the c-fos promoter-chloramphenicol acetyltransferase fusion gene into F-98 cells revealed that activation of c-fos by butyrate was exerted at the promoter level, and sequences located within nucleotides -757 to -402 of the c-fos promoter were responsible for butyrate induction. Our data indicate that transcriptional activation of c-fos through its promoter by butyrate resulted in increased Fos protein expression. Transfection studies show that both c-fos and butyrate activate TRE-containing genes, and fos may be a downstream mediator of butyrate. Furthermore, expression of c-fos plays a major role in modulating the growth properties of F-98 cells.

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Year:  1995        PMID: 7864828      PMCID: PMC1136480          DOI: 10.1042/bj3060047

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  49 in total

1.  Induction of fos and sis proto-oncogenes and genes of the extracellular matrix proteins during butyrate induced glioma differentiation.

Authors:  S J Tang; L W Ko; Y H Lee; F F Wang
Journal:  Biochim Biophys Acta       Date:  1990-01-30

2.  Effect of a dominant inhibitory Ha-ras mutation on neuronal differentiation of PC12 cells.

Authors:  J Szeberényi; H Cai; G M Cooper
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

3.  Nuclear localization of c-Fos, but not v-Fos proteins, is controlled by extracellular signals.

Authors:  P Roux; J M Blanchard; A Fernandez; N Lamb; P Jeanteur; M Piechaczyk
Journal:  Cell       Date:  1990-10-19       Impact factor: 41.582

4.  Requirement for fos gene expression in the transcriptional activation of collagenase by other oncogenes and phorbol esters.

Authors:  A Schönthal; P Herrlich; H J Rahmsdorf; H Ponta
Journal:  Cell       Date:  1988-07-29       Impact factor: 41.582

5.  Different requirements for formation of Jun: Jun and Jun: Fos complexes.

Authors:  T Smeal; P Angel; J Meek; M Karin
Journal:  Genes Dev       Date:  1989-12       Impact factor: 11.361

6.  The c-Fos protein interacts with c-Jun/AP-1 to stimulate transcription of AP-1 responsive genes.

Authors:  R Chiu; W J Boyle; J Meek; T Smeal; T Hunter; M Karin
Journal:  Cell       Date:  1988-08-12       Impact factor: 41.582

7.  fos-associated cellular p39 is related to nuclear transcription factor AP-1.

Authors:  P Sassone-Corsi; W W Lamph; M Kamps; I M Verma
Journal:  Cell       Date:  1988-08-12       Impact factor: 41.582

8.  fos-lacZ transgenic mice: mapping sites of gene induction in the central nervous system.

Authors:  R J Smeyne; K Schilling; L Robertson; D Luk; J Oberdick; T Curran; J I Morgan
Journal:  Neuron       Date:  1992-01       Impact factor: 17.173

9.  c-Jun dimerizes with itself and with c-Fos, forming complexes of different DNA binding affinities.

Authors:  T D Halazonetis; K Georgopoulos; M E Greenberg; P Leder
Journal:  Cell       Date:  1988-12-02       Impact factor: 41.582

10.  Common DNA binding site for Fos protein complexes and transcription factor AP-1.

Authors:  F J Rauscher; L C Sambucetti; T Curran; R J Distel; B M Spiegelman
Journal:  Cell       Date:  1988-02-12       Impact factor: 41.582

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  5 in total

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Journal:  Curr Immunol Rev       Date:  2005-06

2.  The effects of histone acetylation on estrogen responsiveness in MCF-7 cells.

Authors:  M F Ruh; S Tian; L K Cox; T S Ruh
Journal:  Endocrine       Date:  1999-10       Impact factor: 3.633

3.  Activity banding of human chromosomes as shown by histone acetylation.

Authors:  J W Breneman; P M Yau; R R Swiger; R Teplitz; H A Smith; J D Tucker; E M Bradbury
Journal:  Chromosoma       Date:  1996-07       Impact factor: 4.316

4.  Systemic short-chain fatty acids rapidly alter gastrointestinal structure, function, and expression of early response genes.

Authors:  K A Tappenden; M I McBurney
Journal:  Dig Dis Sci       Date:  1998-07       Impact factor: 3.199

Review 5.  Cholesterylbutyrate solid lipid nanoparticles as a butyric acid prodrug.

Authors:  Andrea Brioschi; Gian Paolo Zara; Sara Calderoni; Maria Rosa Gasco; Alessandro Mauro
Journal:  Molecules       Date:  2008-02-01       Impact factor: 4.411

  5 in total

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