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Updated: Sep 10, 2025

Visualization of DNA Repair Proteins Interaction by Immunofluorescence
Published on: June 26, 2020
NSUN2 facilitates DICER cleavage of DNA damage-associated R-loops to promote repair
Adele Alagia1, Kamal Ajit1, Arianna Di Fazio1
1Sir William Dunn School of Pathology, South Parks Road, Oxford, UK.
Abstract:
DNA integrity is constantly challenged by both endogenous and exogenous damaging agents, resulting in various forms of damage. Failure to repair DNA accurately leads to genomic instability, a hallmark of cancer. Distinct pathways exist to repair different types of DNA damage. Double-strand breaks (DSBs) represent a particularly severe form of damage, due to the physical separation of DNA strands. The repair of DSBs requires the activity of RNA Polymerase II (RNAPII) and the generation of Damage-responsive transcripts (DARTs). Here we show that the RNA m5C-methyltransferase NSUN2 localises to DSBs in a transcription-dependent manner, where it binds to and methylates DARTs. The depletion of NSUN2 results in an accumulation of nascent primary DARTs around DSBs. Furthermore, we detect an RNA-dependent interaction between NSUN2 and DICER, which is stimulated by DNA damage. NSUN2 activity promotes DICER cleavage of DARTs-associated R-loops, which is required for efficient DNA repair. We report a role of the RNA m5C -methyltransferase NSUN2 within the RNA-dependent DNA damage response, highlighting its function as a DICER chaperone for the clearance of non-canonical substrates such as DARTs, thereby contributing to genomic integrity.
Insights
The RNA methyltransferase NSUN2 helps repair DNA double-strand breaks (DSBs) by processing damage-responsive transcripts (DARTs). This process is crucial for maintaining genomic integrity and preventing cancer.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- DNA integrity is vital, and its disruption, especially through double-strand breaks (DSBs), can lead to genomic instability and cancer.
- The repair of DSBs involves complex pathways, including RNA Polymerase II (RNAPII) and damage-responsive transcripts (DARTs).
Purpose of the Study:
- To investigate the role of the RNA methyltransferase NSUN2 in DNA double-strand break repair.
- To elucidate the mechanism by which NSUN2 contributes to the RNA-dependent DNA damage response.
Main Methods:
- Localization studies of NSUN2 at DSBs.
- Analysis of DARTs accumulation upon NSUN2 depletion.
- Investigation of NSUN2-DICER interaction in response to DNA damage.
- Assessment of NSUN2's role in DARTs-associated R-loop processing.
Main Results:
- NSUN2 localizes to DSBs in a transcription-dependent manner and methylates DARTs.
- NSUN2 depletion leads to the accumulation of primary DARTs at DSBs.
- NSUN2 interacts with DICER, promoting the cleavage of DARTs-associated R-loops for efficient DNA repair.
Conclusions:
- NSUN2 functions as a key RNA methyltransferase in the DNA damage response pathway.
- NSUN2 acts as a DICER chaperone, clearing non-canonical substrates like DARTs to maintain genomic integrity.
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