Bulged and Canonical G-Quadruplex Conformations Determine NDPK Binding Specificity

Molecules. 2019 May 23;24(10):1988. doi: 10.3390/molecules24101988.

Abstract

Guanine-rich DNA strands can adopt tertiary structures known as G-quadruplexes (G4s) that form when Hoogsteen base-paired guanines assemble as planar stacks, stabilized by a central cation like K+. In this study, we investigated the conformational heterogeneity of a G-rich sequence from the 5' untranslated region of the Zea mays hexokinase4 gene. This sequence adopted an extensively polymorphic G-quadruplex, including non-canonical bulged G-quadruplex folds that co-existed in solution. The nature of this polymorphism depended, in part, on the incorporation of different sets of adjacent guanines into a quadruplex core, which permitted the formation of the different conformations. Additionally, we showed that the maize homolog of the human nucleoside diphosphate kinase (NDPK) NM23-H2 protein-ZmNDPK1-specifically recognizes and promotes formation of a subset of these conformations. Heteromorphic G-quadruplexes play a role in microorganisms' ability to evade the host immune system, so we also discuss how the underlying properties that determine heterogeneity of this sequence could apply to microorganism G4s.

Keywords: G-quadruplex; G4; NDPK; nucleoside diphosphate kinase.

MeSH terms

  • 5' Untranslated Regions
  • Binding Sites
  • Circular Dichroism
  • DNA, Plant / chemistry*
  • DNA, Plant / metabolism
  • G-Quadruplexes
  • Hexokinase / chemistry
  • Hexokinase / genetics*
  • Models, Molecular
  • Nucleoside-Diphosphate Kinase / metabolism*
  • Plant Proteins / chemistry
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Spectrophotometry, Ultraviolet
  • Zea mays / enzymology*
  • Zea mays / genetics

Substances

  • 5' Untranslated Regions
  • DNA, Plant
  • Plant Proteins
  • Hexokinase
  • Nucleoside-Diphosphate Kinase