Regulation of c-fos gene expression in hamster fibroblasts: initiation and elongation of transcription and mRNA degradation.

Abstract:

:Rapid and transient activation of both c-fos transcription and mRNA accumulation occurs when resting CCL39 hamster fibroblasts are serum-stimulated to grow. By using several combinations of serum and cycloheximide, a protein synthesis inhibitor, we showed that: i) addition of cycloheximide to resting cell elicits an increase in c-fos gene transcription located within the first 540 bases of the unit, suggesting that an "attenuation-like" mechanism, similar to that observed for c-myc, might be essential for c-fos transcriptional regulation; ii) it also prevents both transcriptional shutoff and mRNA degradation in serum-stimulated cells; iii) upon removal of cycloheximide, mRNA degradation resumes rapidly; deletion of a 130 bases long segment in the 3 non-coding region leads to a stabilization of c-fos mRNA lending experimental support to a putative destabilizer element within this sequence.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Fort P,Rech J,Vie A,Piechaczyk M,Bonnieu A,Jeanteur P,Blanchard JM

doi

10.1093/nar/15.14.5657

subject

Has Abstract

pub_date

1987-07-24 00:00:00

pages

5657-67

issue

14

eissn

0305-1048

issn

1362-4962

journal_volume

15

pub_type

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