Bypass of complex co-directional replication-transcription collisions by replisome skipping

Nucleic Acids Res. 2021 Sep 27;49(17):9870-9885. doi: 10.1093/nar/gkab760.

Abstract

Collisions between the replisome and RNA polymerases [RNAP(s)] are the main obstacle to DNA replication. These collisions can occur either head-on or co-directionally with respect to the direction of translocation of both complexes. Whereas head-on collisions require additional factors to be resolved, co-directional collisions are thought to be overcome by the replisome itself using the mRNA transcript as a primer. We show that mRNA takeover is utilized primarily after collisions with single RNAP complexes with short transcripts. Bypass of more complex transcription complexes requires the synthesis of a new primer downstream of the RNAP for the replisome to resume leading-strand synthesis. In both cases, bypass proceeds with displacement of the RNAP. Rep, Mfd, UvrD and RNase H can process the RNAP block and facilitate replisome bypass by promoting the formation of continuous leading strands. Bypass of co-directional RNAP(s) and/or R-loops is determined largely by the length of the obstacle that the replisome needs to traverse: R-loops are about equally as potent obstacles as RNAP arrays if they occupy the same length of the DNA template.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacterial Proteins / metabolism
  • DNA Helicases / metabolism
  • DNA Replication*
  • DNA-Directed DNA Polymerase*
  • DNA-Directed RNA Polymerases / metabolism
  • Escherichia coli Proteins / metabolism
  • Multienzyme Complexes*
  • R-Loop Structures
  • RNA, Messenger / metabolism
  • Transcription Factors / metabolism
  • Transcription, Genetic*

Substances

  • Bacterial Proteins
  • Escherichia coli Proteins
  • Multienzyme Complexes
  • RNA, Messenger
  • Transcription Factors
  • rep protein, E coli
  • transcription repair coupling factor protein, Bacteria
  • DNA synthesome
  • DNA-Directed RNA Polymerases
  • DNA-Directed DNA Polymerase
  • UvrD protein, E coli
  • DNA Helicases