How to scan naked DNA using promiscuous recognition and no clamping: a model for pioneer transcription factors

Nucleic Acids Res. 2024 Oct 14;52(18):11098-11114. doi: 10.1093/nar/gkae790.

Abstract

Most DNA scanning proteins uniquely recognize their cognate sequence motif and slide on DNA assisted by some sort of clamping interface. The pioneer transcription factors that control cell fate in eukaryotes must forgo both elements to gain access to DNA in naked and chromatin forms; thus, whether or how these factors scan naked DNA is unknown. Here, we use single-molecule techniques to investigate naked DNA scanning by the Engrailed homeodomain (enHD) as paradigm of highly promiscuous recognition and open DNA binding interface. We find that enHD scans naked DNA quite effectively, and about 200000-fold faster than expected for a continuous promiscuous slide. To do so, enHD scans about 675 bp of DNA in 100 ms and then redeploys stochastically to another location 530 bp afar in just 10 ms. During the scanning phase enHD alternates between slow- and medium-paced modes every 3 and 40 ms, respectively. We also find that enHD binds nucleosomes and does so with enhanced affinity relative to naked DNA. Our results demonstrate that pioneer-like transcription factors can in principle do both, target nucleosomes and scan active DNA efficiently. The hybrid scanning mechanism used by enHD appears particularly well suited for the highly complex genomic signals of eukaryotic cells.

MeSH terms

  • Animals
  • Binding Sites
  • DNA* / chemistry
  • DNA* / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • Homeodomain Proteins* / chemistry
  • Homeodomain Proteins* / genetics
  • Homeodomain Proteins* / metabolism
  • Nucleosomes* / chemistry
  • Nucleosomes* / metabolism
  • Protein Binding
  • Transcription Factors* / metabolism

Substances

  • DNA
  • Nucleosomes
  • Transcription Factors
  • Homeodomain Proteins
  • DNA-Binding Proteins