ANALYSIS OF C-FOS EXPRESSION IN THE BUTYRATE-INDUCED F-98 GLIOMA CELL-DIFFERENTIATION

被引:27
作者
TANG, SJ
HUANG, YM
WANG, FF
机构
[1] NATL YANG MING MED COLL,INST BIOCHEM,TAIPEI 112,TAIWAN
[2] NATL RES INST CHINESE MED,TAIPEI 23117,TAIWAN
[3] NATL OCEAN UNIV,INST MARINE BIOTECHNOL,KEELONG 115,TAIWAN
关键词
D O I
10.1042/bj3060047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:47 / 56
页数:10
相关论文
共 51 条
[1]   MOLECULAR THEMES IN ONCOGENESIS [J].
BISHOP, JM .
CELL, 1991, 64 (02) :235-248
[2]   SODIUM-BUTYRATE ACTIVATES HUMAN-IMMUNODEFICIENCY-VIRUS LONG TERMINAL REPEAT - DIRECTED EXPRESSION [J].
BOHAN, C ;
YORK, D ;
SRINIVASAN, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (03) :899-905
[3]  
BOHAN CA, 1989, VIROLOGY, V172, P572
[4]   PROENKEPHALIN GENE-EXPRESSION IN THE PC12-PHEOCHROMOCYTOMA CELL-LINE - STIMULATION BY SODIUM-BUTYRATE [J].
BYRD, JC ;
NARANJO, JR ;
LINDBERG, I .
ENDOCRINOLOGY, 1987, 121 (04) :1299-1305
[5]  
CHIRGWIN JM, 1978, BIOCHEMISTRY-US, V18, P5294
[6]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[7]   GROWTH-FACTORS IN DEVELOPMENT, TRANSFORMATION, AND TUMORIGENESIS [J].
CROSS, M ;
DEXTER, TM .
CELL, 1991, 64 (02) :271-280
[9]   IDENTIFICATION OF A TRANSCRIPTIONAL ENHANCER ELEMENT UPSTREAM FROM THE PROTO-ONCOGENE FOS [J].
DESCHAMPS, J ;
MEIJLINK, F ;
VERMA, IM .
SCIENCE, 1985, 230 (4730) :1174-1177
[10]   MULTIPLE SEQUENCE ELEMENTS IN THE C-FOS PROMOTER MEDIATE INDUCTION BY CAMP [J].
FISCH, TM ;
PRYWES, R ;
SIMON, MC ;
ROEDER, RG .
GENES & DEVELOPMENT, 1989, 3 (02) :198-211