El-Maarri Osman, Kareta Michael S, Mikeska Thomas, Becker Tim, Diaz-Lacava Amalia, Junen Judith, Nüsgen Nicole, Behne Frank, Wienker Thomas, Waha Andreas, Oldenburg Johannes, Chédin Frédéric
Institute of Experimental Hematology and Transfusion Medicine, University of Bonn, Bonn, Germany.
Hum Mol Genet. 2009 May 15;18(10):1755-68. doi: 10.1093/hmg/ddp088. Epub 2009 Feb 26.
Causes underlying inter-individual variations in DNA methylation profiles among normal healthy populations are not thoroughly understood. To investigate the contribution of genetic variation in DNA methyltransferase (DNMT) genes to such epigenetic variation, we performed a systematic search for polymorphisms in all known human DNMT genes [DNMT1, DNMT3A, DNMT3B, DNMT3L and DNMT2 (TRDMT1)] in 192 healthy males and females. One hundred and eleven different polymorphisms were detected. Of these, 24 were located in coding regions and 10 resulted in an amino acid change that may affect the corresponding DNMT protein structure or function. Association analysis between all major polymorphisms (frequency > 1%) and quantitative DNA methylation profiles did not return significant results after correction for multiple testing. Polymorphisms leading to an amino acid change were further investigated for changes in global DNA methylation by differential methylation hybridization. This analysis revealed that a rare change at DNMT3L (R271Q) was associated with significant DNA hypomethylation. Biochemical characterization confirmed that DNMT3L(R271Q) is impaired in its ability to stimulate de novo DNA methylation by DNMT3A. Methylated DNA immunoprecipitation based analysis using CpG island microarrays revealed that the hypomethylation in this sample preferentially clustered to subtelomeric genomic regions with affected loci corresponding to a subset of repetitive CpG islands with low predicted promoter potential located outside of genes.
正常健康人群中DNA甲基化谱个体间差异的潜在原因尚未完全明确。为了研究DNA甲基转移酶(DNMT)基因中的遗传变异对这种表观遗传变异的贡献,我们对192名健康男性和女性的所有已知人类DNMT基因[DNMT1、DNMT3A、DNMT3B、DNMT3L和DNMT2(TRDMT1)]中的多态性进行了系统搜索。共检测到111种不同的多态性。其中,24种位于编码区,10种导致氨基酸改变,可能影响相应的DNMT蛋白结构或功能。在对多重检验进行校正后,所有主要多态性(频率>1%)与定量DNA甲基化谱之间的关联分析未得出显著结果。通过差异甲基化杂交进一步研究导致氨基酸改变的多态性对整体DNA甲基化的影响。该分析表明,DNMT3L(R271Q)的一种罕见改变与显著的DNA低甲基化有关。生化特性分析证实,DNMT3L(R271Q)刺激DNMT3A从头DNA甲基化的能力受损。使用CpG岛微阵列的基于甲基化DNA免疫沉淀的分析表明,该样本中的低甲基化优先聚集在亚端粒基因组区域,受影响的位点对应于基因外预测启动子潜力较低的重复CpG岛子集。