Probing conformational transitions towards mutagenic Watson-Crick-like G·T mismatches using off-resonance sugar carbon R relaxation dispersion

J Biomol NMR. 2020 Sep;74(8-9):457-471. doi: 10.1007/s10858-020-00337-7. Epub 2020 Aug 12.

Abstract

NMR off-resonance R relaxation dispersion measurements on base carbon and nitrogen nuclei have revealed that wobble G·T/U mismatches in DNA and RNA duplexes exist in dynamic equilibrium with short-lived, low-abundance, and mutagenic Watson-Crick-like conformations. As Watson-Crick-like G·T mismatches have base pairing geometries similar to Watson-Crick base pairs, we hypothesized that they would mimic Watson-Crick base pairs with respect to the sugar-backbone conformation as well. Using off-resonance R measurements targeting the sugar C3' and C4' nuclei, a structure survey, and molecular dynamics simulations, we show that wobble G·T mismatches adopt sugar-backbone conformations that deviate from the canonical Watson-Crick conformation and that transitions toward tautomeric and anionic Watson-Crick-like G·T mismatches restore the canonical Watson-Crick sugar-backbone. These measurements also reveal kinetic isotope effects for tautomerization in D2O versus H2O, which provide experimental evidence in support of a transition state involving proton transfer. The results provide additional evidence in support of mutagenic Watson-Crick-like G·T mismatches, help rule out alternative inverted wobble conformations in the case of anionic G·T-, and also establish sugar carbons as new non-exchangeable probes of this exchange process.

Keywords: Anions; Chemical exchange; Nucleic acid dynamics; Replication error; Sugar pucker; Tautomers.

MeSH terms

  • Base Pair Mismatch*
  • Base Pairing
  • Carbon / chemistry*
  • DNA / chemistry*
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular*
  • Nucleic Acid Conformation*
  • Sugars / chemistry*
  • Thymine

Substances

  • Sugars
  • Carbon
  • DNA
  • Thymine