Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
PLoS One. 2012;7(9):e46295. doi: 10.1371/journal.pone.0046295. Epub 2012 Sep 26.
In order to comprehensively screen genetic variants leading to differential expression of the important human ABCB1 gene in the primary drug-metabolizing organ, ABCB1 mRNA expression levels were measured in 73 normal liver tissue samples from Chinese subjects. A set of Tag SNPs. were genotyped. In addition, imputation was performed within a 500 kb region around the ABCB1 gene using the reference panels of 1,000 Genome project and HapMap III. Bayesian regression was used to assess the strength of associations by compute Bayes Factors for imputed SNPs. Through imputation and linkage disequilibrium analysis, the imputed loci rs28373093, rs1002205, rs1029421, rs2285647, and rs10235835, may represent independent and strong association signals. rs28373093, a polymorphism 1.5 kb upstream from the ABCB1 transcription start site, has the strongest association. 2677 G>A/T and 3435C>T confer a clear gene-dosage effect on ABCB1 mRNA expression. The systematic characterization of gene-wide common quantitative trait loci associated with ABCB1 mRNA expression in normal liver tissues would provide the candidate markers to ABCB1-relevant clinical phenotypes in Chinese population.
为了全面筛选导致重要的人类 ABCB1 基因在主要药物代谢器官中差异表达的遗传变异,我们测量了来自中国受试者的 73 个正常肝组织样本中的 ABCB1 mRNA 表达水平。一组 Tag SNPs 被分型。此外,还使用 1000 基因组计划和 HapMap III 的参考面板,在 ABCB1 基因周围 500 kb 区域内进行了内插。贝叶斯回归用于通过计算内插 SNP 的贝叶斯因子来评估关联的强度。通过内插和连锁不平衡分析,内插的 rs28373093、rs1002205、rs1029421、rs2285647 和 rs10235835 位点可能代表独立且强的关联信号。rs28373093 是 ABCB1 转录起始位点上游 1.5 kb 的多态性,与 ABCB1 mRNA 表达的关联最强。2677 G>A/T 和 3435C>T 对 ABCB1 mRNA 表达具有明显的基因剂量效应。对与正常肝组织中 ABCB1 mRNA 表达相关的全基因组常见数量性状基因座进行系统表征,将为中国人群中与 ABCB1 相关的临床表型提供候选标记。