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

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.

Publication DOI: https://doi.org/10.1016/j.cell.2014.03.048
Divisions: College of Health & Life Sciences > Aston Medical School
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
Additional Information: This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
Uncontrolled Keywords: General Biochemistry,Genetics and Molecular Biology
Publication ISSN: 1097-4172
Last Modified: 13 Nov 2024 17:43
Date Deposited: 09 Nov 2018 16:08
Full Text Link:
Related URLs: http://www.scop ... tnerID=8YFLogxK (Scopus URL)
PURE Output Type: Article
Published Date: 2014-05-22
Authors: Saponaro, Marco
Kantidakis, Theodoros (ORCID Profile 0000-0002-3515-5235)
Mitter, Richard
Kelly, Gavin P.
Heron, Mark
Williams, Hannah
Söding, Johannes
Stewart, Aengus
Svejstrup, Jesper Q.

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