Hinge like domain motion facilitates human RBMS1 protein binding to proto-oncogene c-myc promoter

Nucleic Acids Res. 2021 Jun 4;49(10):5943-5955. doi: 10.1093/nar/gkab363.

Abstract

DNA binding proteins recognize DNA specifically or non-specifically using direct and indirect readout mechanisms like sliding, hopping, and diffusion. However, a common difficulty in explicitly elucidating any particular mechanism of site-specific DNA-protein recognition is the lack of knowledge regarding target sequences and inadequate account of non-specific interactions, in general. Here, we decipher the structural basis of target search performed by the key regulator of expression of c-myc proto-oncogene, the human RBMS1 protein. In this study, we have shown the structural reorganization of this multi-domain protein required for recognizing the specific c-myc promoter sequence. The results suggest that a synergy between structural re-organization and thermodynamics is necessary for the recognition of target sequences. The study presents another perspective of looking at the DNA-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Calorimetry, Differential Scanning
  • Crystallography, X-Ray
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / genetics
  • Gene Expression
  • Genes, myc*
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Dynamics Simulation
  • Mutagenesis, Site-Directed
  • Promoter Regions, Genetic*
  • Protein Binding
  • Protein Domains
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc / chemistry*
  • Proto-Oncogene Proteins c-myc / genetics*
  • RNA-Binding Proteins / chemistry*
  • RNA-Binding Proteins / genetics
  • Recombinant Proteins
  • Thermodynamics

Substances

  • DNA-Binding Proteins
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc
  • RBMS1 protein, human
  • RNA-Binding Proteins
  • Recombinant Proteins