Abstract
We previously found three transcription factor-binding motifs in the rat p53 promoter. They are two recognition motifs of NF1-Iike protein (NF1-like element 1: -296 ∼ -312, NF1-like element 2: -195 ∼ -219) and a bHLH protein binding element (-142 ∼ -146). In this study, we investigated the DNA-protein complex formation of the three elements with nuclear extracts from both normal and regenerating liver to find the element involved in the induced transcription of p53. The level of each DNA-protein complex on NF1-like and bHLH motifs was not changed. Instead, a new element located at -264 ∼ -284 was detected in the DNase I footprinting assay with regenerating nuclear extract. This element has partial homology to the AP1 consensus motif. However, the competition studies with diverse oligonucleotides suggest that the binding protein is not AP1. An in vitro transcription assay shows that this element is important for the transcriptional activation of the rat p53 promoter. Therefore, for the induced transcription of the rat p53 promoter, the -264 ∼ -284 region is required in addition to two NF1-like and one bHLH motif.
Original language | English |
---|---|
Pages (from-to) | 45-50 |
Number of pages | 6 |
Journal | Journal of Biochemistry and Molecular Biology |
Volume | 32 |
Issue number | 1 |
State | Published - 31 Jan 1999 |
Keywords
- AP1
- BHLH
- Liver regeneration
- Transcription regulation
- p53 gene