Epigenetic regulation of inflammation by CxxC domain-containing proteins*

被引:8
|
作者
Onodera, Atsushi [1 ,2 ]
Kiuchi, Masahiro [1 ]
Kokubo, Kota [1 ]
Nakayama, Toshinori [1 ,3 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Immunol, Chiba, Japan
[2] Chiba Univ, Inst Global Prominent Res, Chiba, Japan
[3] AMED, AMED CREST, Chiba, Japan
关键词
DNA methylation; helper T cells; ten-eleven translocation (TET) proteins; trithorax; ACTIVE DNA DEMETHYLATION; BASE-RESOLUTION ANALYSIS; GENOME-WIDE ANALYSIS; CPG BINDING-PROTEIN; T-CELL DEVELOPMENT; 5-METHYLCYTOSINE OXIDATION; GENE-EXPRESSION; THYMINE DNA; STEM-CELLS; TRANSCRIPTIONAL REGULATION;
D O I
10.1111/imr.13056
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epigenetic regulation of gene transcription in the immune system is important for proper control of protective and pathogenic inflammation. Aberrant epigenetic modifications are often associated with dysregulation of the immune cells, including lymphocytes and macrophages, leading to pathogenic inflammation and autoimmune diseases. Two classical epigenetic markers-histone modifications and DNA cytosine methylation, the latter is the 5 position of the cytosine base in the context of CpG dinucleotides-play multiple roles in the immune system. CxxC domain-containing proteins, which basically bind to the non-methylated CpG (i.e., epigenetic "readers"), often function as "writers" of the epigenetic markers via their catalytic domain within the proteins or by interacting with other epigenetic modifiers. We herein report the most recent advances in our understanding of the functions of CxxC domain-containing proteins in the immune system and inflammation, mainly focusing on T cells and macrophages.
引用
收藏
页码:137 / 151
页数:15
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