Abstract
The mouse insulin-like growth factor II gene (Igf2) is transcribed from three promoters (P1, P2 and P3), and is expressed in a tissue-specific and developmentally regulated fashion; however, little information is available on the transcription factors controlling Igf2 expression. The AP-1 complex is a transcription factor involved in the regulation of a variety of genes, including those encoding certain growth factors. We show that Igf2 P3 is transactivated by AP-1 in a transient expression assay, and that this effect is mediated through two non-consensus AP-1 binding sites characterised by DNA-protein interaction studies. Mutational analysis indicates these sites are required for AP-1 responsiveness and full promoter activity.
| Original language | English |
|---|---|
| Pages (from-to) | 1873-9 |
| Number of pages | 7 |
| Journal | Nucleic Acids Research |
| Volume | 21 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 25 Apr 1993 |
Keywords
- Animals
- Base Sequence
- Binding Sites
- Blotting, Northern
- Cell Differentiation
- Cell Line
- DNA
- Insulin-Like Growth Factor II
- Mice
- Molecular Sequence Data
- Promoter Regions, Genetic
- Proto-Oncogene Proteins c-jun
- Rats
- Stem Cells
- Transcriptional Activation
- Journal Article
- Research Support, Non-U.S. Gov't
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