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PMID: 9341107 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Heat shock factor 1 represses Ras-induced transcriptional activation of the c-fos gene.

The Journal of biological chemistry ·Vol. 272 ·No. 43 ·1997-10-24 ·Pages 26803-6

Chen C, Xie Y, Stevenson MA, Auron PE, Calderwood SK

Abstract

Heat shock factor 1, the critical molecular regulator of the stress response is conserved throughout eukaryotic organisms and activates the transcription of heat shock genes. We now show that heat shock factor 1 inhibits the expression of c-fos, an immediate early gene that controls responses to extracellular stimuli for growth and differentiation. Heat shock factor 1 inhibits the transcription of the c-fos gene and antagonizes the activating effects of the signal transducing protein Ras on the c-fos promoter and on the promoter of another Ras responsive gene uPA. This property was specific for heat shock factor 1; c-fos repression was not seen with the structurally related protein heat shock factor 2. Repression involved different molecular mechanisms compared with those involved in transcriptional activation by heat shock factor 1 and specifically did not require binding to the c-fos promoter. Thus, in addition to its known role as a transcriptional activator of the cellular heat shock response, heat shock factor 1 also antagonizes the expression of Fos, a key component of the ubiquitous AP-1 transcription factor complex and as such could influence multiple aspects of cell regulation.

MeSH Terms
Animals CHO Cells Cricetinae DNA-Binding Proteins/biosynthesis,metabolism Genes, Reporter Genes, fos Heat Shock Transcription Factors Heat-Shock Proteins/biosynthesis,metabolism Humans Luciferases/biosynthesis Promoter Regions, Genetic Proto-Oncogene Proteins c-fos/biosynthesis Proto-Oncogene Proteins p21(ras)/biosynthesis,metabolism Recombinant Fusion Proteins/biosynthesis Transcription Factors/biosynthesis,metabolism Transcription, Genetic Transfection Urokinase-Type Plasminogen Activator/biosynthesis beta-Galactosidase/biosynthesis
Chemicals
DNA-Binding Proteins Heat Shock Transcription Factors Heat-Shock Proteins Proto-Oncogene Proteins c-fos Recombinant Fusion Proteins Transcription Factors HSF2 protein, human Luciferases beta-Galactosidase Urokinase-Type Plasminogen Activator HRAS protein, human Proto-Oncogene Proteins p21(ras)
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Chen C
Dana-Farber Cancer Institute and Joint Center for Radiation Therapy, Harvard Medical School, Boston, Massachusetts 02115, USA.
Xie Y
Stevenson M A
Auron P E
Calderwood S K
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1997-10-24
Pages
26803-6
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA31303 · United States
NCI NIH HHS · CA4707 · United States
NCI NIH HHS · CA50642 · United States
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