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Updated: Jun 11, 2025

Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
Published on: June 8, 2018
From silence to symphony: transcriptional repression and recovery in response to DNA damage
Kamal Ajit1, Monika Gullerova1
1Sir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Abstract:
Genotoxic stress resulting from DNA damage is resolved through a signaling cascade known as the DNA Damage Response (DDR). The repair of damaged DNA is essential for cell survival, often requiring the DDR to attenuate other cellular processes such as the cell cycle, DNA replication, and transcription of genes not involved in DDR. The complex relationship between DDR and transcription has only recently been investigated. Transcription can facilitate the DDR in response to double-strand breaks (DSBs) and stimulate nucleotide excision repair (NER). However, transcription may need to be reduced to prevent potential interference with the repair machinery. In this review, we discuss various mechanisms that regulate transcription repression in response to different types of DNA damage, categorizing them by their range and duration of effect. Finally, we explore various models of transcription recovery following DNA damage-induced repression.
Insights
The DNA Damage Response (DDR) manages DNA repair, sometimes by reducing transcription to aid healing. This review explores how transcription is repressed and recovers after DNA damage.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- DNA damage triggers the DNA Damage Response (DDR) pathway essential for cell survival.
- DDR signaling often involves attenuating cellular processes like cell cycle, DNA replication, and transcription.
- The interplay between DDR and transcription is a recent area of investigation.
Purpose of the Study:
- To review mechanisms regulating transcription repression in response to DNA damage.
- To categorize these mechanisms by their range and duration of effect.
- To explore models of transcription recovery post-DNA damage.
Main Methods:
- Literature review of studies on DNA Damage Response and transcription.
- Analysis of mechanisms controlling transcription repression.
- Categorization of repression mechanisms based on effect scope and persistence.
- Examination of transcription recovery models.
Main Results:
- Transcription can facilitate DDR and nucleotide excision repair (NER) after double-strand breaks (DSBs).
- Repression of transcription is often necessary to prevent interference with DNA repair machinery.
- Mechanisms of transcription repression vary in range and duration.
Conclusions:
- Understanding transcription regulation during DDR is crucial for comprehending cell survival strategies.
- Diverse mechanisms ensure efficient DNA repair while minimizing transcriptional interference.
- Further research into transcription recovery models will illuminate cellular resilience post-damage.
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