Nature Communications · 2022 · 65 citations · 59 references
Life SciencesGeneticsMolecular BiologyDna RepairTranscriptionTranscriptional RegulationDna DamageDna Damage SignalingDna Strand BreaksPromoter RegulationRna Polymerase RegulationTranscription ElongationDegradationDna Damage Response PathwaysDna Damage ResponsesGenotoxic Stress ResponseRna Polymerase Ii FunctionRna Polymerase Ii RegulationTranscription-coupled Dna RepairTranscription-coupled Repair Defects
The precise regulation of RNA Polymerase II (Pol II) transcription after genotoxic stress is crucial for proper execution of the DNA damage-induced stress response. While stalling of Pol II on transcription-blocking lesions (TBLs) blocks transcript elongation and initiates DNA repair in cis, TBLs additionally elicit a response in trans that regulates transcription genome-wide. Here we uncover that, after an initial elongation block in cis, TBLs trigger the genome-wide VCP-mediated proteasomal degradation of promoter-bound, P-Ser5-modified Pol II in trans. This degradation is mechanistically distinct from processing of TBL-stalled Pol II, is signaled via GSK3, and contributes to the TBL-induced transcription block, even in transcription-coupled repair-deficient cells. Thus, our data reveal the targeted degradation of promoter-bound Pol II as a critical pathway that allows cells to cope with DNA damage-induced transcription stress and enables the genome-wide adaptation of transcription to genotoxic stress.
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