Integrator facilitates RNAPII removal to prevent transcription-replication collisions and genome instability

Rahul Bhowmick*, Kavi P.M. Mehta, Mads Lerdrup, David Cortez

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

23 Citations (Scopus)
21 Downloads (Pure)

Abstract

DNA replication preferentially initiates close to active transcription start sites (TSSs) in the human genome. Transcription proceeds discontinuously with an accumulation of RNA polymerase II (RNAPII) in a paused state near the TSS. Consequently, replication forks inevitably encounter paused RNAPII soon after replication initiates. Hence, dedicated machinery may be needed to remove RNAPII and facilitate unperturbed fork progression. In this study, we discovered that Integrator, a transcription termination machinery involved in the processing of RNAPII transcripts, interacts with the replicative helicase at active forks and promotes the removal of RNAPII from the path of the replication fork. Integrator-deficient cells have impaired replication fork progression and accumulate hallmarks of genome instability including chromosome breaks and micronuclei. The Integrator complex resolves co-directional transcription-replication conflicts to facilitate faithful DNA replication.

Original languageEnglish
JournalMolecular Cell
Volume83
Issue number13
Pages (from-to)2357-2366.e8
ISSN1097-2765
DOIs
Publication statusPublished - 2023

Bibliographical note

Publisher Copyright:
© 2023 Elsevier Inc.

Keywords

  • fork reversal
  • genome stability
  • Integrator complex
  • MCM complex
  • R-loop
  • replication stress
  • replicative helicase
  • RNA polymerase II
  • RNAPII
  • transcription-replication conflicts
  • TRCs

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