Dissection of functional NF-Y-RFX cooperative interactions on the MHC class II Ea promoter

J Mol Biol. 2000 Sep 22;302(3):539-52. doi: 10.1006/jmbi.2000.4028.

Abstract

Transcription of major histocompatibility complex (MHC) class II genes depends upon the trimeric complexes RFX and NF-Y binding to the conserved X-Y promoter elements. We produced and purified the RFX subunits from Escherichia coli, reconstituted DNA-binding to the mouse Ea X box and dissected the interactions with NF-Y. RFX and NF-Y do not interact in solution, but make cooperative interactions in EMSA: a minimal NF-Y, composed of the evolutionary conserved domains, is sufficient and the RFXAP N-terminal half is expendable. Altering the X-Y distance abolishes cooperativity, indicating that DNA imposes severe spatial constraints. When tested on a highly positioned nucleosome, RFX binds DNA well and NF-Y does not increase its affinity further. Transfections of NF-Y subunits, but not RFX, in class II negative cells improves basal transcription and coexpression of the two activators has a synergistic effect, while modestly increasing CIITA-mediated activation. These results show that interactions between the two trimers on DNA are key to MHC class II expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • CCAAT-Enhancer-Binding Proteins
  • Cell Line
  • Conserved Sequence / genetics
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Genes, MHC Class II / genetics*
  • Kinetics
  • Mice
  • Mutation
  • Nuclear Proteins*
  • Nucleic Acid Conformation
  • Nucleosomes / chemistry
  • Nucleosomes / genetics
  • Nucleosomes / metabolism
  • Precipitin Tests
  • Promoter Regions, Genetic / genetics*
  • Protein Binding
  • Recombinant Proteins / metabolism
  • Regulatory Factor X Transcription Factors
  • Response Elements / genetics
  • Thermodynamics
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic / genetics
  • Transcriptional Activation / genetics
  • Transfection

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • MHC class II transactivator protein
  • Nuclear Proteins
  • Nucleosomes
  • Recombinant Proteins
  • Regulatory Factor X Transcription Factors
  • Trans-Activators
  • Transcription Factors
  • DNA

Grants and funding