Inoue Shinichi, Oishi Michio
Kazusa Research Institute, 2-6-7, Kazusa-kamatari, Kisarazu, Chiba 292-0818, Japan.
Gene. 2005 Mar 28;348:123-34. doi: 10.1016/j.gene.2004.12.044.
We have studied the effects of methylation of the promoter region on the expression of human synaptotagmin XI (syt11), a gene implicated in the onset of schizophrenia. Sequence analysis showed that cytosine residues not in the CpG sequence, but still within the promoter region of the gene, are partially methylated. The methylated cytosine residues are located in the mRNA-coding (minus) strand of the promoter region (mCmCTTmCTTmCmC). Gel mobility shift assays showed that when the cytosine residues are methylated, the binding activity of an Sp family protein, a transcription factor, to the region is significantly reduced. Furthermore, transient transcription assays using artificially methylated promoter sequences showed that methylation did reduce the expression of the reporter gene. The biological significance of the finding is discussed in respect to the effect of methylation of non-CpG sequences in promoter regions on gene expression.
我们研究了启动子区域甲基化对人类突触结合蛋白XI(syt11)表达的影响,该基因与精神分裂症的发病有关。序列分析表明,基因启动子区域内不在CpG序列中的胞嘧啶残基部分被甲基化。甲基化的胞嘧啶残基位于启动子区域的mRNA编码(负)链上(mCmCTTmCTTmCmC)。凝胶迁移率变动分析表明,当胞嘧啶残基甲基化时,转录因子Sp家族蛋白与该区域的结合活性显著降低。此外,使用人工甲基化启动子序列的瞬时转录分析表明,甲基化确实降低了报告基因的表达。我们从启动子区域非CpG序列甲基化对基因表达的影响方面讨论了这一发现的生物学意义。