Role of Histone Tails and Single Strand DNA Breaks in Nucleosomal Arrest of RNA Polymerase

Int J Mol Sci. 2023 Jan 24;24(3):2295. doi: 10.3390/ijms24032295.

Abstract

Transcription through nucleosomes by RNA polymerases (RNAP) is accompanied by formation of small intranucleosomal DNA loops (i-loops). The i-loops form more efficiently in the presence of single-strand breaks or gaps in a non-template DNA strand (NT-SSBs) and induce arrest of transcribing RNAP, thus allowing detection of NT-SSBs by the enzyme. Here we examined the role of histone tails and extranucleosomal NT-SSBs in i-loop formation and arrest of RNAP during transcription of promoter-proximal region of nucleosomal DNA. NT-SSBs present in linker DNA induce arrest of RNAP +1 to +15 bp in the nucleosome, suggesting formation of the i-loops; the arrest is more efficient in the presence of the histone tails. Consistently, DNA footprinting reveals formation of an i-loop after stalling RNAP at the position +2 and backtracking to position +1. The data suggest that histone tails and NT-SSBs present in linker DNA strongly facilitate formation of the i-loops during transcription through the promoter-proximal region of nucleosomal DNA.

Keywords: DNA damage; DNA loop; chromatin structure; nucleosome; single-strand DNA breaks; transcription-coupled DNA repair.

MeSH terms

  • DNA / genetics
  • DNA Breaks, Single-Stranded
  • DNA, Single-Stranded
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism
  • Histones* / genetics
  • Histones* / metabolism
  • Nucleosomes* / genetics
  • RNA Polymerase II / genetics
  • Transcription, Genetic

Substances

  • Nucleosomes
  • Histones
  • RNA Polymerase II
  • DNA-Directed RNA Polymerases
  • DNA
  • DNA, Single-Stranded