Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto Japan.
Genet Mol Biol. 2010 Oct;33(4):615-26. doi: 10.1590/s1415-47572010000400004. Epub 2010 Dec 1.
Research has been conducted to identify sequence polymorphisms of gene promoter regions in patients and control subjects, including normal individuals, and to determine the influence of these polymorphisms on transcriptional regulation in cells that express wild-type or mutant p53. In this study we isolated genomic DNA from whole blood of healthy Japanese individuals and sequenced the promoter regions of the MDM2, p53, and p16(INK4a) genes. We identified polymorphisms comprising 3 nucleotide substitutions at exon 1 and intron 1 regions of the MDM2 gene and 1 nucleotide insertion at a poly(C) nucleotide position in the p53 gene. The Japanese individuals also exhibited p16(INK4a) polymorphisms at several positions, including position -191. Reporter gene analysis by using luciferase revealed that the polymorphisms of MDM2, p53, and p16(INK4a) differentially altered luciferase activities in several cell lines, including the Colo320DM, U251, and T98G cell lines expressing mutant p53. Our results indicate that the promoter sequences of these genes differ among normal Japanese individuals and that polymorphisms can alter gene transcription activity.
已经进行了研究,以确定患者和对照受试者(包括正常个体)中基因启动子区域的序列多态性,并确定这些多态性对表达野生型或突变型 p53 的细胞中转录调节的影响。在这项研究中,我们从健康的日本个体的全血中分离基因组 DNA,并对 MDM2、p53 和 p16(INK4a)基因的启动子区域进行测序。我们确定了 MDM2 基因的外显子 1 和内含子 1 区域的 3 个核苷酸取代和 p53 基因中多聚(C)核苷酸位置的 1 个核苷酸插入的多态性。日本个体还在多个位置表现出 p16(INK4a)多态性,包括位置 -191。使用荧光素酶的报告基因分析表明,MDM2、p53 和 p16(INK4a)的多态性在包括表达突变型 p53 的 Colo320DM、U251 和 T98G 细胞系在内的几种细胞系中差异地改变了荧光素酶活性。我们的结果表明,这些基因的启动子序列在正常日本个体中存在差异,并且多态性可以改变基因转录活性。