Publication | Open Access
Regulation of the Th1 Genomic Locus from <i>Ifng</i> through <i>Tmevpg1</i> by T-bet
108
Citations
33
References
2014
Year
GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsEpigeneticsTranscriptional RegulationLong Non-coding RnaMolecular SignalingTh1 Genomic LocusTmevpg1 TranscriptionLncrna Tmevpg1Gene ExpressionEpigenetic RegulationFunctional GenomicsCell BiologyTranscription RegulationChromatin FunctionGene FunctionChromatinChromatin StructureImmune Cell DevelopmentNatural SciencesGene RegulationGenetic MechanismTranscription FactorsMedicineTmevpg1 ProximalCell DevelopmentNon-coding Rna
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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