School of Public Health, Sun Yat-sen University, Guangzhou, People's Republic of China.
Mutat Res. 2011 Nov 1;716(1-2):66-75. doi: 10.1016/j.mrfmmm.2011.08.004. Epub 2011 Aug 26.
The serine-threonine protein phosphatase 2A (PP2A) is a heterotrimeric enzyme family that plays an essential regulatory role in cell growth, differentiation, and apoptosis. Mutations in the genes encoding PP2A-Aα/β subunits are associated with tumorigenesis and other human diseases. To explore whether genetic variations in the promoter region of the PP2A-Aα gene (PPP2R1A) and their frequent haplotypes in the Han Chinese population have an impact on transcriptional activity, we collected DNA samples from 63 healthy Chinese donors and searched for genetic variations in the 5'-flanking promoter region of PPP2R1A (PPP2R1Ap). Haplotypes were characterized by Haploview analysis and individual subcloning. A set of molecular and functional experiments was performed using reporter genes and electrophoretic mobility shifting assay (EMSA). Seven genetic variations were identified within the promoter locus (2038bp) of PPP2R1A. Linkage disequilibrium (LD) patterns and haplotype profiles were analyzed using the identified genetic variants. Using serially truncated human PPP2R1A promoter luciferase constructs, we found that a 685bp (-448nt to +237nt) fragment around the transcription start site (TSS) was the core promoter region. Individual subcloning revealed the existence of six haplotypes in this proximal promoter region of PPP2R1Ap. Using luciferase reporter assays, we found that different haplotypes bearing different variant alleles exhibit distinct promoter activities. The EMSA revealed that the -241 -/G variant influences DNA-protein interactions involving the transcription factor NF-κB, which may regulate the activity of the PPP2R1A proximal promoter. Our findings suggest that functional genetic variants in the proximal promoter of the PP2A-Aα gene and their haplotypes are critical in the regulation of transcriptional activation.
丝氨酸-苏氨酸蛋白磷酸酶 2A(PP2A)是一种异三聚体酶家族,在细胞生长、分化和凋亡中发挥重要的调节作用。编码 PP2A-Aα/β亚基的基因突变与肿瘤发生和其他人类疾病有关。为了探讨 PP2A-Aα 基因(PPP2R1A)启动子区域的遗传变异及其在汉族人群中的常见单倍型是否影响转录活性,我们从 63 名健康的中国供体中收集 DNA 样本,并在 PPP2R1A 的 5'-侧翼启动子区域(PPP2R1Ap)中搜索遗传变异。通过 Haploview 分析和个体亚克隆来描述单倍型。使用报告基因和电泳迁移率变动分析(EMSA)进行了一组分子和功能实验。在 PPP2R1A 的启动子基因座(2038bp)内鉴定出 7 种遗传变异。使用鉴定出的遗传变异分析了连锁不平衡(LD)模式和单倍型谱。使用串联截断的人 PPP2R1A 启动子荧光素酶构建体,我们发现转录起始位点(TSS)周围的 685bp(-448nt 至+237nt)片段是核心启动子区域。个体亚克隆揭示了 PPP2R1Ap 近端启动子区域存在六种单倍型。使用荧光素酶报告基因检测,我们发现具有不同变异等位基因的不同单倍型表现出不同的启动子活性。EMSA 显示-241/-G 变异影响涉及转录因子 NF-κB 的 DNA-蛋白相互作用,这可能调节 PPP2R1A 近端启动子的活性。我们的研究结果表明,PP2A-Aα 基因近端启动子中的功能性遗传变异及其单倍型在转录激活的调节中至关重要。