Epigenetic activation and silencing of the gene that encodes IFN-γ

被引:37
作者
Aune, Thomas M. [1 ,2 ]
Collins, Patrick L. [2 ]
Collier, Sarah P. [2 ]
Henderson, Melodie A. [1 ]
Chang, Shaojing [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
来源
FRONTIERS IN IMMUNOLOGY | 2013年 / 4卷
基金
美国国家卫生研究院;
关键词
interferon-gamma; T helper cells; natural killer cells; natural killer T cells; epigenetics; CpG methylation; long non-coding RNA;
D O I
10.3389/fimmu.2013.00112
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transcriptional activation and repression of genes that are developmentally regulated or exhibit cell-type specific expression patterns is largely achieved by modifying the chromatin template at a gene locus. Complex formation of stable epigenetic histone marks, loss or gain of DNA methylation, alterations in chromosome conformation, and specific utilization of both proximal and distal transcriptional enhancers and repressors all contribute to this process. In addition, long non-coding RNAs are a new species of regulatory RNAs that either positively or negatively regulate transcription of target gene loci. IFN-gamma is a pro-inflammatory cytokine with critical functions in both innate and adaptive arms of the immune system. This review focuses on our current understanding of how the chromatin template is modified at the I FNG locus during developmental processes leading to its transcriptional activation and silencing.
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页数:8
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