The Brn-3a POU family transcription factor stimulates p53 gene expression in human and mouse tumour cells

被引:10
作者
Budhram-Mahadeo, V
Morris, P
Ndisang, D
Irshad, S
Lozano, G
Pedley, B
Latchman, DS
机构
[1] UCL, Inst Child Hlth, London WC1N 1EH, England
[2] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[3] Royal Free & Univ Coll Med Sch, Dept Oncol, London, England
关键词
apoptosis; transcriptional regulation; Brn-3a transcription factor; p53;
D O I
10.1016/S0304-3940(02)00813-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 4
页数:4
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