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Updated: Apr 29, 2026

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Published on: January 31, 2018
[The post-transcriptional regulation of the DNA damage response]
Deling Lin1, Ying Luo2, Yi Song3
1Medical Faculty of Kunming University of Science and Technology, Kunming 650500, China; Institute of Radiation Medicine, Academy of Military Medical Sciences, Beijing 100850, China.
Abstract:
In response to DNA damage, a complex signaling network called DNA damage response (DDR) would be activated in cells, to arrest the cell cycle and initiate DNA repair. Previous studies were mainly focused on the transcriptional regulation of gene and covalent modification of protein. In recent years, mRNA stability and translation in DDR attracted more and more attention. Emerging evidence suggests that microRNAs and RNA-binding proteins (RBPs) play critical roles in protecting the heritable genome through participating in the regulation of the DNA damage response. In this review, we discuss the most recent findings regarding the post-transcriptional regulation of the DDR by microRNAs and RBPs.
Insights
The DNA damage response (DDR) involves microRNAs and RNA-binding proteins (RBPs) in regulating cellular repair mechanisms. This review highlights their crucial roles in post-transcriptional control of the DDR pathway.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Context:
- The DNA damage response (DDR) is a critical cellular network activated by DNA damage to halt cell division and initiate repair.
- Research traditionally focused on transcriptional and protein modification aspects of DDR.
- Recent attention has shifted towards the roles of mRNA stability and translation in DDR.
Purpose:
- To review recent findings on the post-transcriptional regulation of the DNA damage response (DDR).
- To highlight the involvement of microRNAs and RNA-binding proteins (RBPs) in DDR.
- To discuss how these molecules contribute to genome protection.
Summary:
- MicroRNAs and RBPs are increasingly recognized for their roles in the DDR.
- These molecules regulate DDR through post-transcriptional mechanisms, affecting mRNA stability and translation.
- Their collective action is vital for maintaining genomic integrity following DNA damage.
Impact:
- Advances understanding of DDR regulation beyond transcriptional control.
- Identifies novel targets for therapeutic interventions in diseases involving DNA damage.
- Provides insights into the complex interplay of RNA molecules in cellular stress responses.
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