Regulation of the Th1 genomic locus from Ifng through Tmevpg1 by T-bet

J Immunol. 2014 Oct 15;193(8):3959-65. doi: 10.4049/jimmunol.1401099. Epub 2014 Sep 15.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Lineage / immunology
  • Enhancer Elements, Genetic*
  • Epigenesis, Genetic*
  • Genetic Loci
  • Interferon-gamma / genetics*
  • Mice
  • Mice, Inbred BALB C
  • Proto-Oncogene Protein c-ets-1 / metabolism
  • RNA, Long Noncoding / genetics*
  • Regulatory Sequences, Nucleic Acid / genetics
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism*
  • Th1 Cells / immunology*
  • Transcription Factor RelA / metabolism

Substances

  • Ets1 protein, mouse
  • Proto-Oncogene Protein c-ets-1
  • RNA, Long Noncoding
  • Rela protein, mouse
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Tmevpg1 long noncoding RNA, mouse
  • Transcription Factor RelA
  • Interferon-gamma