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The Brn-3a POU family transcription factor stimulates p53 gene expression in human and mouse tumour cells.
- Source :
-
Neuroscience letters [Neurosci Lett] 2002 Dec 06; Vol. 334 (1), pp. 1-4. - Publication Year :
- 2002
-
Abstract
- The Brn-3a POU family transcription factor is able to induce the expression of genes encoding anti-apoptotic proteins such as Bcl-2 and Bcl-x and protects neuronal cells from apoptosis. This effect is opposed by the pro-apoptotic p53 protein which completely inhibits the ability of Brn-3a to activate the Bcl-2 and Bcl-x promoters. Here we demonstrate that Brn-3a is able to stimulate p53 expression. Thus, in co-transfection experiments, Brn-3a activates the p53 promoter acting via a region from +22 to +67, located between the most proximal (+1) and the most distal (+105) transcriptional start sites. Similarly, reduction of Brn-3a expression using anti-sense constructs reduces endogenous p53 expression in human neuroblastoma or cervical carcinoma cell lines growing in vitro and as tumours in nude mice whilst increasing Brn-3a levels enhances p53 expression. These results suggest the existence of a negative feedback loop in which elevated Brn-3a expression induces the expression of p53 which, in turn, antagonises the anti-apoptotic activity of Brn-3a.<br /> (Copyright 2002 Elsevier Science Ireland Ltd.)
- Subjects :
- Animals
Apoptosis genetics
Apoptosis physiology
Carcinoma, Squamous Cell
DNA-Binding Proteins antagonists & inhibitors
DNA-Binding Proteins biosynthesis
Humans
Mice
Mice, Nude
Neuroblastoma
Promoter Regions, Genetic
Transcription Factor Brn-3
Transcription Factor Brn-3A
Transcription Factors antagonists & inhibitors
Transcription Factors biosynthesis
Transcription Factors physiology
Transcriptional Activation physiology
Transfection
Tumor Cells, Cultured
Tumor Suppressor Protein p53 biosynthesis
DNA-Binding Proteins genetics
Transcription Factors genetics
Transcriptional Activation genetics
Tumor Suppressor Protein p53 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0304-3940
- Volume :
- 334
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Neuroscience letters
- Publication Type :
- Academic Journal
- Accession number :
- 12431761
- Full Text :
- https://doi.org/10.1016/s0304-3940(02)00813-3