Department of Medicine, Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Department of Medicine, Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Simpson Querrey Center for Epigenetics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Transl Res. 2019 Feb;204:1-18. doi: 10.1016/j.trsl.2018.08.001. Epub 2018 Aug 9.
DNA methylation is a dynamic epigenetic modification with a prominent role in determining mammalian cell development, lineage identity, and transcriptional regulation. Primarily linked to gene silencing, novel technologies have expanded the ability to measure DNA methylation on a genome-wide scale and uncover context-dependent regulatory roles. The immune system is a prototypic model for studying how DNA methylation patterning modulates cell type- and stimulus-specific transcriptional programs. Preservation of host defense and organ homeostasis depends on fine-tuned epigenetic mechanisms controlling myeloid and lymphoid cell differentiation and function, which shape innate and adaptive immune responses. Dysregulation of these processes can lead to human immune system pathology as seen in blood malignancies, infections, and autoimmune diseases. Identification of distinct epigenotypes linked to pathogenesis carries the potential to validate therapeutic targets in disease prevention and management.
DNA 甲基化是一种动态的表观遗传修饰,在决定哺乳动物细胞发育、谱系身份和转录调控方面发挥着重要作用。主要与基因沉默相关,新的技术已经扩展了在全基因组范围内测量 DNA 甲基化的能力,并揭示了与上下文相关的调节作用。免疫系统是研究 DNA 甲基化模式如何调节细胞类型和刺激特异性转录程序的典型模型。宿主防御和器官稳态的维持依赖于精细调控的表观遗传机制,这些机制控制着髓系和淋巴系细胞的分化和功能,从而塑造先天和适应性免疫反应。这些过程的失调可导致人类免疫系统疾病,如血液恶性肿瘤、感染和自身免疫性疾病。鉴定与发病机制相关的独特表型有可能在疾病预防和管理中验证治疗靶点。