| Literature DB >> 27851891 |
Barbara Steurer1, Jurgen A Marteijn2.
Abstract
The faithful transcription of eukaryotic genes by RNA polymerase II (RNAP2) is crucial for proper cell function and tissue homeostasis. However, transcription-blocking DNA lesions of both endogenous and environmental origin continuously challenge the progression of elongating RNAP2. The stalling of RNAP2 on a transcription-blocking lesion triggers a series of highly regulated events, including RNAP2 processing to make the lesion accessible for DNA repair, R-loop-mediated DNA damage signaling, and the initiation of transcription-coupled DNA repair. The correct execution and coordination of these processes is vital for resuming transcription following the successful repair of transcription-blocking lesions. Here, we outline recent insights into the molecular consequences of RNAP2 stalling on transcription-blocking DNA lesions and how these lesions are resolved to restore mRNA synthesis.Keywords: DNA damage; RNA polymerase 2; nucleotide excision repair; transcription coupled repair; transcription restart
Mesh:
Substances:
Year: 2016 PMID: 27851891 DOI: 10.1016/j.jmb.2016.11.006
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469