RECQL5 controls transcript elongation and suppresses genome instability associated with transcription stress

Research output: Contribution to journalJournal articleResearchpeer-review

  • Marco Saponaro
  • Theodoros Kantidakis
  • Richard Mitter
  • Gavin P. Kelly
  • Mark Heron
  • Hannah Williams
  • Johannes Söding
  • Aengus Stewart
  • Svejstrup, Jesper Qualmann

RECQL5 is the sole member of the RECQ family of helicases associated with RNA polymerase II (RNAPII). We now show that RECQL5 is a general elongation factor that is important for preserving genome stability during transcription. Depletion or overexpression of RECQL5 results in corresponding shifts in the genome-wide RNAPII density profile. Elongation is particularly affected, with RECQL5 depletion causing a striking increase in the average rate, concurrent with increased stalling, pausing, arrest, and/or backtracking (transcription stress). RECQL5 therefore controls the movement of RNAPII across genes. Loss of RECQL5 also results in the loss or gain of genomic regions, with the breakpoints of lost regions located in genes and common fragile sites. The chromosomal breakpoints overlap with areas of elevated transcription stress, suggesting that RECQL5 suppresses such stress and its detrimental effects, and thereby prevents genome instability in the transcribed region of genes.

Original languageEnglish
JournalCell
Volume157
Issue number5
Pages (from-to)1037-1049
Number of pages13
ISSN0092-8674
DOIs
Publication statusPublished - 2014
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by grants from Association for International Cancer Research, the European Research Council, and Cancer Research UK (to J.Q.S.). We thank Nick Matthews and staff in the Advanced Sequencing Facility for their contribution; the Cell Services facility for assistance with cell lines; and members of the Svejstrup laboratory for comments on the manuscript.

ID: 330898891