Modifying the helical structure of DNA by design: recruitment of an architecture-specific protein to an enforced DNA bend

Chem Biol. 1995 Apr;2(4):213-21. doi: 10.1016/1074-5521(95)90271-6.

Abstract

Background: Proteins can force DNA to adopt distorted helical structures that are rarely if ever observed in naked DNA. The ability to synthesize DNA that contains defined helical aberrations would offer a new avenue for exploring the structural and energetic plasticity of DNA. Here we report a strategy for the enforcement of non-canonical helical structures through disulfide cross-linking; this approach is exemplified by the design and synthesis of an oligonucleotide containing a pronounced bend.

Results: A localized bend was site-specifically introduced into DNA by the formation of a disulfide cross-link between the 5' adenines of a 5'-AATT-3' region in complementary strands of DNA. The DNA bend was characterized by high-resolution NMR structure determination of a cross-linked dodecamer and electrophoretic mobility assays on phased multimers, which together indicate that the cross-linked tetranucleotide induces a helical bend of approximately 30 degrees and a modest degree of unwinding. The enforced bend was found to stimulate dramatically the binding of an architecture-specific protein, HMG-D, to the DNA. DNase I foot-printing analysis revealed that the protein is recruited to the section of DNA that is bent.

Conclusions: The present study reports a novel approach for the investigation of non-canonical DNA structures and their recognition by architecture-specific proteins. The mode of DNA bending induced by disulfide cross-linking resembles that observed in structures of protein-DNA complexes. The results reveal common elements in the DNA-binding mode employed by sequence-specific and architecture-specific HMG proteins.

Publication types

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

MeSH terms

  • Cross-Linking Reagents
  • DNA / chemical synthesis*
  • DNA / chemistry*
  • DNA Footprinting
  • Deoxyribonuclease I / chemistry
  • Disulfides / chemistry
  • Electrophoresis, Polyacrylamide Gel
  • High Mobility Group Proteins / chemistry
  • Nuclear Magnetic Resonance, Biomolecular
  • Nucleic Acid Conformation
  • Oligonucleotides / chemistry
  • Proteins / chemistry

Substances

  • Cross-Linking Reagents
  • Disulfides
  • High Mobility Group Proteins
  • Oligonucleotides
  • Proteins
  • DNA
  • Deoxyribonuclease I