The Journal of Immunology · 2014 · 109 citations · 33 references
MedicineImmunologyMolecular BiologyEpigeneticsGene ExpressionTranscriptional RegulationEnhancer ArchitectureEnhancer FunctionImmune Gene RegulationInterferon ResponsesNoncoding Rna FunctionEnhancer-mediated Immune RegulationEnhancer-mediated Transcription ControlEnhancersLineage-specific EnhancersLineage-specific Gene ExpressionLong Noncoding Rna RegulationNoncoding Rna RegulationNoncoding Rna-mediated Regulation
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 lncRNA 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-κB and Ets-1, to the locus. Activities of Tmevpg1-specific enhancers and Tmevpg1 transcription are dependent upon NF-κB. 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.
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