X box-like sequences in the MHC class II region maintain regulatory function

J Immunol. 2005 Jul 15;175(2):1030-40. doi: 10.4049/jimmunol.175.2.1030.

Abstract

Sequences homologous to the canonical MHC class II (MHC-II) gene X box regulatory elements were identified within the HLA-DR subregion of the human MHC and termed X box-like (XL) sequences. Several XL box sequences were found to bind the MHC class II-specific transcription factors regulatory factor X and CIITA and were transcriptionally active. The histone code associated with the XL boxes and that of the HLA-DRA X box was determined. Using CIITA-positive and -negative B cell lines, CIITA-specific histone modifications were identified and found to be consistent among the active XL boxes. Although a remarkable similarity was observed for most modifications, differences in magnitude between the HLA-DRA promoter for modifications associated with the assembly of the general transcription factors, such as histone H3 lysine 9 acetylation and H3 lysine 4 trimethylation, distinguished the very active HLA-DRA promoter from the XL box regions. In response to IFN-gamma, XL box-containing histones displayed increased acetylation, coincident with CIITA expression and that observed in B cells, suggesting that the end point mechanisms of chromatin remodeling for cell type-specific MHC-II expression were similar. Lastly, an interaction between one XL box and the HLA-DRA promoter was observed in a chromatin-looping assay. Therefore, these data provide evidence that certain XL box sequences contribute to a global increase in chromatin accessibility of the HLA-DR region in B lymphocytes and in response to IFN-gamma and supports the involvement of these XL sequences in the regulation of MHC-II genes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylation
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Chromatin / genetics
  • Chromatin / immunology
  • Chromatin / metabolism
  • DNA Methylation
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / isolation & purification
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology*
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic / immunology*
  • Genes, MHC Class II*
  • HLA-D Antigens / genetics*
  • HLA-D Antigens / metabolism*
  • HLA-DR Antigens / genetics
  • HLA-DR Antigens / metabolism
  • HLA-DR alpha-Chains
  • Histones / metabolism
  • Humans
  • Interferon-gamma / pharmacology
  • Nuclear Proteins / isolation & purification
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology
  • Oligonucleotide Array Sequence Analysis
  • Protein Binding / genetics
  • Protein Binding / immunology
  • Regulatory Factor X Transcription Factors
  • Trans-Activators / isolation & purification
  • Trans-Activators / metabolism
  • Trans-Activators / physiology
  • Transcription Factors / genetics
  • Transcription Factors / isolation & purification
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*

Substances

  • Chromatin
  • DNA-Binding Proteins
  • HLA-D Antigens
  • HLA-DR Antigens
  • HLA-DR alpha-Chains
  • Histones
  • MHC class II transactivator protein
  • Nuclear Proteins
  • Regulatory Factor X Transcription Factors
  • Trans-Activators
  • Transcription Factors
  • Interferon-gamma