Regulation of the Th1 Genomic Locus from Ifng through Tmevpg1 by T-bet

被引:98
作者
Collier, Sarah P. [1 ]
Henderson, Melodie A. [2 ]
Tossberg, John T. [2 ]
Aune, Thomas M. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
LONG NONCODING RNA; INTERFERON-GAMMA LOCUS; CELL-DIFFERENTIATION; GENE-EXPRESSION; TRANSCRIPTION FACTOR; EPIGENETIC CONTROL; NATURAL-KILLER; CHROMATIN; PROMOTER; RESPONSES;
D O I
10.4049/jimmunol.1401099
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Long noncoding RNAs (lncRNAs), critical regulators of protein-coding genes, are likely to be coexpressed with neighboring protein-coding genes in the genome. How the genome integrates signals to achieve coexpression of lncRNA genes and neighboring protein-coding genes is not well understood. The IncRNA Tmevpg1 (NeST, Ifng-AS1) is critical for Th1-lineage-specific expression of Ifng and is coexpressed with Ifng. In this study, we show that T-bet guides epigenetic remodeling of Tmevpg1 proximal and distal enhancers, leading to recruitment of stimulus-inducible transcription factors, NF-kappa B and Ets-1, to the locus. Activities of Tmevpg1-specific enhancers and Tmevpg1 transcription are dependent upon NF-kappa B. Thus, we propose that T-bet stimulates epigenetic remodeling of Tmevpg1-specific enhancers and Ifng-specific enhancers to achieve Th1-lineage-specific expression of Ifng.
引用
收藏
页码:3959 / 3965
页数:7
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