Elongation Factor TFIIS Prevents Transcription Stress and R-Loop Accumulation to Maintain Genome Stability
Description
Although correlations between RNA polymerase II (RNAPII) transcription stress, R-loops, and genome instability have been established, the mechanisms underlying these connections remain poorly understood. Here, we used a mutant version of the transcription elongation factor TFIIS (TFIISmut), aiming to specifically induce increased levels of RNAPII pausing, arrest, and/or backtracking in human cells. Indeed, TFIISmut expression results in slower elongation rates, relative depletion of polymerases from the end of genes, and increased levels of stopped RNAPII; it affects mRNA splicing and termination as well. Remarkably, TFIISmut expression also dramatically increases R-loops, which may form at the anterior end of backtracked RNAPII and trigger genome instability, including DNA strand breaks. These results shed light on the relationship between transcription stress and R-loops and suggest that different classes of R-loops may exist, potentially with distinct consequences for genome stability.
Abstract
Cancer Research UK FC001166
Abstract
UK Medical Research Council FC001166
Abstract
Wellcome Trust FC001166
Abstract
European Research Council 693327, ERC2014 AdG669898
Abstract
Ministerio de Economía y Competitividad BFU2013-42918-P, BFU2016-75058-P
Additional details
- URL
- https://idus.us.es/handle//11441/90721
- URN
- urn:oai:idus.us.es:11441/90721
- Origin repository
- USE