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

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

Research output: Contribution to journalArticlepeer-review

103 Citations (Scopus)

Abstract

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
Pages (from-to)1037-49
Number of pages13
JournalCell
Volume157
Issue number5
Early online date15 May 2014
DOIs
Publication statusPublished - 22 May 2014

Keywords

  • Genome, Human
  • Genomic Instability
  • HEK293 Cells
  • Humans
  • RNA Polymerase II
  • RecQ Helicases
  • Transcription Elongation, Genetic
  • Transcription, Genetic

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