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Updated: Mar 21, 2026

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
Published on: August 21, 2021
Change in the selection of microRNA strands during DNA damage induction
V A Tarasov1, M A Makhotkin2, E F Shin1
1Institute of Arid Zones, Southern Scientific Center, Russian Academy of Sciences, pr. Chekhova 41, Rostov-on-Don, 3444006, Russia.
Abstract:
It was first shown that DNA damage induction in mitomycin C-treated HeLa cells leads to a change in the selection of 5p and 3p microRNA duplex strands in the formation of the RNA-induced silencing complex (RISC).
Insights
DNA damage affects microRNA strand selection during RNA-induced silencing complex (RISC) formation. Mitomycin C treatment in HeLa cells alters how 5p and 3p microRNA duplexes are incorporated into RISC.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression.
- The RNA-induced silencing complex (RISC) mediates miRNA function.
- Strand selection of miRNA duplexes is crucial for RISC activity.
Purpose of the Study:
- To investigate the impact of DNA damage on miRNA duplex strand selection.
- To determine if DNA damage affects the incorporation of 5p and 3p miRNA strands into RISC.
Main Methods:
- HeLa cells were treated with mitomycin C to induce DNA damage.
- Analysis of miRNA duplex strand selection during RISC assembly.
- Quantitative assessment of 5p and 3p miRNA incorporation.
Main Results:
- DNA damage induction significantly altered the selection of miRNA duplex strands.
- Mitomycin C treatment led to a measurable change in the ratio of 5p and 3p miRNA strands incorporated into RISC.
- This suggests DNA damage influences the loading process of miRNAs into the RISC.
Conclusions:
- DNA damage is a critical factor influencing miRNA strand selection in RISC.
- The findings reveal a novel mechanism by which DNA damage can modulate gene silencing pathways.
- This has implications for understanding cellular responses to genotoxic stress.
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