Ortmann Christina A, Burchert Andreas, Hölzle Katharina, Nitsche Andreas, Wittig Burghardt, Neubauer Andreas, Schmidt Manuel
Klinik für Hämatologie, Onkologie and Immunologie, Zentrum Innere Medizin, Klinikum der Philipps-Universität, Marburg, Germany.
Nucleic Acids Res. 2005 Dec 7;33(21):6895-905. doi: 10.1093/nar/gki1001. Print 2005.
Although the bcr-abl translocation has been shown to be the causative genetic aberration in chronic myeloid leukemia (CML), there is mounting evidence that the deregulation of other genes, such as the transcription factor interferon regulatory factor 4 (IRF-4), is also implicated in the pathogenesis of CML. Promoter methylation of CpG target sites or direct deletions/insertions of genes are mechanisms of a reversible or permanent silencing of gene expression, respectively. Therefore, we investigated whether IRF-4 promoter methylation or mutation may be involved in the regulation of IRF-4 expression in leukemia cells. Whereas promoter mutations or structural rearrangements could be excluded as a cause of altered IRF-4 expression in hematopoietic cells, the IRF-4 promoter methylation status was found to significantly influence IRF-4 transcription. First, treatment of IRF-4-negative lymphoid, myeloid and monocytic cell lines with the methylation-inhibitor 5-aza-2-deoxycytidine resulted in a time- and concentration-dependent increase of IRF-4 mRNA and protein levels. Second, using a restriction-PCR-assay and bisulfite-sequencing we identified specifically methylated CpG sites in IRF-4-negative but not in IRF-4-positive cells. Third, we clearly determined promoter methylation as a mechanism for IRF-4 down-regulation via reporter gene assays, but did not detect an association of methylational status and mRNA expression of DNA methyltransferases or methyl-CpG-binding proteins. Together, these data suggest CpG site-specific IRF-4 promoter methylation as a putative mechanism of down-regulated IRF-4 expression in leukemia.
尽管bcr-abl易位已被证明是慢性髓性白血病(CML)的致病基因畸变,但越来越多的证据表明,其他基因的失调,如转录因子干扰素调节因子4(IRF-4),也与CML的发病机制有关。CpG靶位点的启动子甲基化或基因的直接缺失/插入分别是基因表达可逆或永久沉默的机制。因此,我们研究了IRF-4启动子甲基化或突变是否可能参与白血病细胞中IRF-4表达的调控。虽然启动子突变或结构重排可被排除为造血细胞中IRF-4表达改变的原因,但发现IRF-4启动子甲基化状态显著影响IRF-4转录。首先,用甲基化抑制剂5-氮杂-2'-脱氧胞苷处理IRF-4阴性的淋巴细胞、髓细胞和单核细胞系,导致IRF-4 mRNA和蛋白水平呈时间和浓度依赖性增加。其次,使用限制性PCR分析和亚硫酸氢盐测序,我们在IRF-4阴性而非IRF-4阳性细胞中鉴定出特异性甲基化的CpG位点。第三,我们通过报告基因分析明确确定启动子甲基化是IRF-4下调的机制,但未检测到DNA甲基转移酶或甲基-CpG结合蛋白的甲基化状态与mRNA表达之间的关联。总之,这些数据表明CpG位点特异性IRF-4启动子甲基化是白血病中IRF-4表达下调的一种可能机制。