NMR investigation of FOXO4-DNA interaction for discriminating target and non-target DNA sequences

Commun Biol. 2024 Nov 1;7(1):1425. doi: 10.1038/s42003-024-07133-1.

Abstract

Forkhead box O4 (FOXO4), a human transcription factor, recognizes target DNA through its forkhead domain (FHD) while maintaining comparable binding affinity to non-target DNA. The conserved region 3 (CR3), a transactivation domain, modulates DNA binding kinetics to FHD and contributes to target DNA selection, but the underlying mechanism of this selection remains elusive. Using paramagnetic relaxation enhancement analysis, we observed a minor state of CR3 close to FHD in the presence of non-target DNA, a state absent when FHD interacts with target DNA. This minor state suggests that CR3 effectively masks the non-target DNA-binding interface on FHD. The interaction weakens significantly under high salt concentration, implying that CR3 or high salt concentrations can modulate electrostatic interactions with non-target DNA. Our 15N relaxation measurements revealed FHD's flexibility with non-target DNA and increased rigidity with target DNA binding. Our findings offer insights into the role of FOXO4 as a transcription initiator.

MeSH terms

  • Base Sequence
  • Binding Sites
  • Cell Cycle Proteins* / chemistry
  • Cell Cycle Proteins* / genetics
  • Cell Cycle Proteins* / metabolism
  • DNA* / chemistry
  • DNA* / metabolism
  • Forkhead Transcription Factors* / chemistry
  • Forkhead Transcription Factors* / genetics
  • Forkhead Transcription Factors* / metabolism
  • Humans
  • Magnetic Resonance Spectroscopy / methods
  • Models, Molecular
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Binding*

Substances

  • FOXO4 protein, human
  • DNA
  • Forkhead Transcription Factors
  • Cell Cycle Proteins