首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The Brn-3a POU family transcription factor stimulates p53 gene expression in human and mouse tumour cells.
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The Brn-3a POU family transcription factor stimulates p53 gene expression in human and mouse tumour cells.

机译:Brn-3a POU家族转录因子刺激人和小鼠肿瘤细胞中的p53基因表达。

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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. Copyright 2002 Elsevier Science Ireland Ltd.
机译:Brn-3a POU家族转录因子能够诱导编码抗凋亡蛋白(例如Bcl-2和Bcl-x)的基因表达,并保护神经元细胞免于凋亡。促凋亡的p53蛋白可完全抑制Brn-3a激活Bcl-2和Bcl-x启动子的能力,而与之相反。在这里,我们证明Brn-3a能够刺激p53表达。因此,在共转染实验中,Brn-3a激活p53启动子,其作用范围是从+22至+67,位于最接近的(+1)和最远端的(+105)转录起始位点之间。类似地,使用反义构建体降低Brn-3a表达可降低人成神经细胞瘤或宫颈癌细胞系中体外生长的裸鼠体内肿瘤中的内源性p53表达,同时增加Brn-3a水平可增强p53表达。这些结果表明存在负反馈环,其中升高的Brn-3a表达诱导p53的表达,其反过来拮抗Brn-3a的抗凋亡活性。版权所有2002 Elsevier Science Ireland Ltd.

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