Abstract
The retinoblastoma (Rb) protein is a master regulator of cell cycle. Accumulating evidence suggests that elevation of Rb expression is a key event in differentiation of various cell types. However the mechanism of regulation of Rb expression is poorly understood. Here we report that the candidate oncoprotein Bcl-3, previously characterized as a member of the IκB family, activates transcription of the Rb gene, whose promoter has no typical κB sites. A target element for Bcl-3 that matches the consensus for the E4TF1/GABP transcription factor was identified. Bcl-3 was shown to promote tetramer formation of E4TF1. During muscle cell differentiation, increased bcl-3 expression was observed before the induction of the Rb mRNA. Transient expression of Bcl-3 in myoblasts was shown to induce expression of the endogenous Rb. Furthermore, expression of the antisense bcl-3 RNA in myoblasts suppressed induction of Rb and myogenic differentiation. These results suggest that Bcl-3 is an upstream regulator of Rb expression during differentiation of muscle cells.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1837-1845 |
| Number of pages | 9 |
| Journal | Oncogene |
| Volume | 12 |
| Issue number | 9 |
| State | Published - 1996 |
Keywords
- Bcl-3
- E4TF1
- GABP
- Muscle differentiation
- Rb
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Cancer Research
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