CBFbeta allosterically regulates the Runx1 Runt domain via a dynamic conformational equilibrium

Nat Struct Mol Biol. 2004 Sep;11(9):901-6. doi: 10.1038/nsmb819. Epub 2004 Aug 22.

Abstract

Core binding factors (CBFs) are heterodimeric transcription factors consisting of a DNA-binding CBFalpha subunit and non-DNA-binding CBFbeta subunit. The CBFbeta subunit increases the affinity of the DNA-binding Runt domain of CBFalpha for DNA while making no direct contacts to the DNA. We present evidence for conformational exchange in the S-switch region in a Runt domain-DNA complex that is quenched upon CBFbeta binding. Analysis of (15)N backbone relaxation parameters shows that binding of CBFbeta reduces the backbone dynamics in the microsecond-to-millisecond time frame for several regions of the Runt domain that make energetically important contacts with the DNA. The DNA also undergoes conformational exchange in the Runt domain-DNA complex that is quenched in the presence of CBFbeta. Our results indicate that allosteric regulation by the CBFbeta subunit is mediated by a shift in an existing dynamic conformational equilibrium of both the Runt domain and DNA.

Publication types

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

MeSH terms

  • Allosteric Site
  • Binding Sites
  • Calorimetry
  • Core Binding Factor Alpha 2 Subunit
  • DNA / chemistry
  • DNA-Binding Proteins / chemistry*
  • Dimerization
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Nitrogen / chemistry
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins / chemistry*
  • Time Factors
  • Transcription Factor AP-2
  • Transcription Factors / chemistry*

Substances

  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Transcription Factor AP-2
  • Transcription Factors
  • DNA
  • Nitrogen

Associated data

  • PDB/1H9D