Abstract
The serum response element (SRE) contributes to transcriptional repression of the c-fos proto-oncogene. We show that the transcription factor SRF is able to repress SRE-dependent transcription, apparently by sequestering a co-activator. Only the DNA-binding core region is required for this SRE-dependent repression. Furthermore the phosphorylation status at potential casein kinase II sites within an N-terminal repression domain affects SRE-independent transcription. SRF may thus pleiotropically influence cellular transcription, representing a novel aspect of SRF function.
Original language | English |
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Pages (from-to) | 45-9 |
Number of pages | 5 |
Journal | FEBS Letters |
Volume | 357 |
Issue number | 1 |
DOIs | |
Publication status | Published - 02 Jan 1995 |