The role of the minor groove substituents in indirect readout of DNA sequence by 434 repressor

J Biol Chem. 2003 Apr 11;278(15):12955-60. doi: 10.1074/jbc.M212667200. Epub 2003 Feb 4.

Abstract

The sequence of non-contacted bases at the center of the 434 repressor binding site affects the strength of the repressor-DNA complex by influencing the structure and flexibility of DNA (Koudelka, G. B., and Carlson, P. (1992) Nature 355, 89-91). We synthesized 434 repressor binding sites that differ in their central sequence base composition to test the importance of minor groove substituents and/or the number of base pair hydrogen bonds between these base pairs on DNA structure and strength of the repressor-DNA complex. We show here that the number of base pair H-bonds between the central bases apparently has no role in determining the relative affinity of a DNA site for repressor. Instead we find that the affinity of DNA for repressor depends on the absence or presence the N2-NH(2) group on the purine bases at the binding site center. The N2-NH(2) group on bases at the center of the 434 binding site appears to destabilize 434 repressor-DNA complexes by decreasing the intimacy of the specific repressor-DNA contacts, while increasing the reliance on protein contacts to the DNA phosphate backbone. Thus, the presence of an N2-NH(2) group on the purines at the center of a binding site globally alters the precise conformation of the protein-DNA interface.

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Base Pairing
  • Base Sequence
  • Binding Sites
  • Circular Dichroism
  • Hydroxyl Radical
  • Kinetics
  • Nucleic Acid Conformation
  • Osmolar Concentration
  • Protein Conformation
  • Repressor Proteins / chemistry*
  • Repressor Proteins / genetics*
  • Thermodynamics
  • Viral Proteins

Substances

  • 434-repressor protein, Bacteriophage 434
  • Repressor Proteins
  • Viral Proteins
  • Hydroxyl Radical