TET Methylcytosine Oxidases in T Cell and B Cell Development and Function

被引:54
|
作者
Tsagaratou, Ageliki [1 ]
Lio, Chan-Wang J. [1 ]
Yue, Xiaojing [1 ]
Rao, Anjana [1 ,2 ,3 ]
机构
[1] La Jolla Inst Allergy & Immunol, Dept Signaling & Gene Express, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Pharmacol & Moores Canc Ctr, La Jolla, CA 92093 USA
[3] Sanford Consortium Regenerat Med, La Jolla, CA 92037 USA
来源
FRONTIERS IN IMMUNOLOGY | 2017年 / 8卷
关键词
TET proteins; 5hmC; T cells; B cells; development; immune gene regulation; chromatin accessibility; cancer; DNA METHYLTRANSFERASE 1; GENE-EXPRESSION; 5-METHYLCYTOSINE OXIDATION; FOXP3; EXPRESSION; LINEAGE SPECIFICATION; DYNAMIC CHANGES; CIS-ELEMENT; METHYLATION; 5-HYDROXYMETHYLCYTOSINE; DEMETHYLATION;
D O I
10.3389/fimmu.2017.00220
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 established by DNA methyltransferases and is a key epigenetic mark. Ten-eleven translocation (TET) proteins are enzymes that oxidize 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further oxidization products (oxi-mCs), which indirectly promote DNA demethylation. Here, we provide an overview of the effect of TET proteins and altered DNA modification status in T and B cell development and function. We summarize current advances in our understanding of the role of TET proteins and 5hmC in T and B cells in both physiological and pathological contexts. We describe how TET proteins and 5hmC regulate DNA modification, chromatin accessibility, gene expression, and transcriptional networks and discuss potential underlying mechanisms and open questions in the field.
引用
收藏
页数:15
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