Department of Biology, University of Pisa, Via Derna 1, Pisa, Italy.
Hum Mutat. 2010 Apr;31(4):456-65. doi: 10.1002/humu.21214.
The transcription of the DeltaN133p53 isoform of the TP53 gene is controlled by an internal promoter region (IPR) containing eight polymorphisms in 11 common haplotypes, following a resequencing of 47 Caucasians. We assayed the functional effects of the commonest six haplotypes on the promoter activity with a luciferase reporter system, in HeLa and 293T cells. These studies showed that different IPR haplotypes are associated with differences in the promoter activity resulting in marked variation in the baseline expression of DeltaN133p53. In vivo quantitative-polymerase chain reaction (PCR) on human tissues confirmed that the baseline levels of DeltaN133p53 showed haplotype specific differences that paralleled those seen in vitro. When cell lines were treated with camptothecin, the fold-increase in DeltaN133p53 levels was dose-dependent but haplotype-independent (i.e., similar for all the haplotypes). Finally, we used an electrophoretic mobility shift assay to analyze the rs1794287 polymorphism and found changes in the pattern of protein binding. This partially confirmed our in silico analysis showing that the polymorphism rs1794287 can affect the function of the internal promoter by changing its affinity for several transcription factors. Thus, we showed that the expression of DeltaN133p53 is under genetic control, and suggested the presence of interindividual differences underlying this mechanism.
TP53 基因的 DeltaN133p53 异构体的转录受包含 11 个常见单倍型中 8 个多态性的内部启动子区域(IPR)控制,这是对 47 名高加索人进行重测序后的结果。我们使用荧光素酶报告系统在 HeLa 和 293T 细胞中检测了最常见的六种单倍型对启动子活性的功能影响。这些研究表明,不同的 IPR 单倍型与启动子活性的差异相关,导致 DeltaN133p53 的基础表达发生明显变化。对人体组织进行的体内定量聚合酶链反应(PCR)证实,DeltaN133p53 的基础水平表现出与体外所见相似的单倍型特异性差异。当细胞系用喜树碱处理时,DeltaN133p53 水平的增加倍数与剂量呈依赖性但与单倍型无关(即,所有单倍型相似)。最后,我们使用电泳迁移率变动分析来分析 rs1794287 多态性,发现蛋白结合模式发生变化。这部分证实了我们的计算机分析,表明多态性 rs1794287 可以通过改变其与几个转录因子的亲和力来影响内部启动子的功能。因此,我们表明 DeltaN133p53 的表达受遗传控制,并表明这种机制存在个体间差异。