Blood Bank, Preveza General Hospital, Preveza, Greece.
Molecular Biology Laboratory, Ioannina University Hospital, Ioannina, Greece.
Cell Mol Life Sci. 2018 Jun;75(11):1999-2009. doi: 10.1007/s00018-018-2783-2. Epub 2018 Feb 26.
DNA methylation (CpG methylation) exerts an important role in normal differentiation and proliferation of hematopoietic stem cells and their differentiated progeny, while it has also the ability to regulate myeloid versus lymphoid fate. Mutations of the epigenetic machinery are observed in hematological malignancies including acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) resulting in hyper- or hypo-methylation affecting several different pathways. Enhancers are cis-regulatory elements which promote transcription activation and are characterized by histone marks including H3K27ac and H3K4me1/2. These gene subunits are target gene expression 'fine-tuners', are differentially used during the hematopoietic differentiation, and, in contrast to promoters, are not shared by the different hematopoietic cell types. Although the interaction between gene promoters and DNA methylation has extensively been studied, much less is known about the interplay between enhancers and DNA methylation. In hematopoiesis, DNA methylation at enhancers has the potential to discriminate between fetal and adult erythropoiesis, and also is a regulatory mechanism in granulopoiesis through repression of neutrophil-specific enhancers in progenitor cells during maturation. The interplay between DNA methylation at enhancers is disrupted in AML and MDS and mainly hyper-methylation at enhancers raising early during myeloid lineage commitment is acquired during malignant transformation. Interactions between mutated epigenetic drivers and other oncogenic mutations also affect enhancers' activity with final result, myeloid differentiation block. In this review, we have assembled recent data regarding DNA methylation and enhancers' activity in normal and mainly myeloid malignancies.
DNA 甲基化(CpG 甲基化)在造血干细胞及其分化产物的正常分化和增殖中发挥重要作用,同时也具有调节髓系与淋系命运的能力。表观遗传机制的突变在包括急性髓系白血病(AML)和骨髓增生异常综合征(MDS)在内的血液恶性肿瘤中被观察到,导致超甲基化或低甲基化,影响几个不同的途径。增强子是顺式调控元件,可促进转录激活,其特征是组蛋白标记,包括 H3K27ac 和 H3K4me1/2。这些基因亚基是靶基因表达的“微调器”,在造血分化过程中被不同地使用,与启动子不同,它们不被不同的造血细胞类型共享。尽管基因启动子和 DNA 甲基化之间的相互作用已被广泛研究,但增强子和 DNA 甲基化之间的相互作用知之甚少。在造血中,增强子上的 DNA 甲基化有可能区分胎儿和成人红细胞生成,并且在粒细胞生成中也是一种调节机制,通过在成熟过程中抑制祖细胞中的中性粒细胞特异性增强子来抑制其表达。AML 和 MDS 中增强子上的 DNA 甲基化相互作用被破坏,主要是在髓系谱系承诺早期获得的增强子高甲基化,发生在恶性转化期间。突变的表观遗传驱动因子和其他致癌突变之间的相互作用也会影响增强子的活性,最终导致髓系分化受阻。在这篇综述中,我们汇集了有关正常和主要髓系恶性肿瘤中 DNA 甲基化和增强子活性的最新数据。