DNA methylation as a transcriptional regulator of the immune system

被引:94
|
作者
Morales-Nebreda, Luisa [2 ]
Mclafferty, Fred S. [2 ]
Singer, Benjamin D. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Pulm & Crit Care Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Pulm & Crit Care Med, Dept Med, Chicago, IL 60611 USA
关键词
ACUTE MYELOID-LEUKEMIA; EPIGENOME-WIDE ASSOCIATION; T-CELL DEVELOPMENT; HEMATOPOIETIC STEM; DNMT3A MUTATIONS; CLONAL HEMATOPOIESIS; METHYLTRANSFERASE; GENE-EXPRESSION; SELF-RENEWAL; IN-VIVO;
D O I
10.1016/j.trsl.2018.08.001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:1 / 18
页数:18
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