Methylation and demethylation in the regulation of genes, cells, and responses in the immune system

被引:102
|
作者
Fitzpatrick, DR
Wilson, CB
机构
[1] Amgen Inc, Immunol Syst Dept, Seattle, WA 98101 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
关键词
DE-NOVO METHYLATION; IFN-GAMMA PROMOTER; DNA METHYLTRANSFERASE GENE; CPG-BINDING PROTEIN; HISTONE DEACETYLASE COMPLEX; T-HELPER LYMPHOCYTES; LOCUS-CONTROL REGION; HUMAN CANCER-CELLS; EPIGENETIC REGULATION; INTERLEUKIN-2; GENE;
D O I
10.1016/S1521-6616(03)00205-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA methylation is a focus of epigenetic research in the immune system. This overview begins with a synopsis of the players and processes involved in DNA methylation, demethylation, methyl-CpG-recognition, histone modification, and chromatin remodeling. The role of these mechanisms in immune responses, with a focus on T lymphocytes, is then reviewed. There is evidence for epigenetic regulation of several key immune processes including thymocyte development, antigen presentation, differentiation, cytokine expression, effector function, and memory. DNA methylation contributes, along with other epigenetic mechanisms, to the establishment of transcriptional thresholds that vary between genes and T cell types. The immune system is a fertile field for studies of epigenetic regulation of cell fate and function. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:37 / 45
页数:9
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