# Visualizing DNA repair factor recruitment at sites of transcription in single cells

**Authors:** Tianyi Guan, Yuepeng Shi, Tae-Hee Lee, Philipp Oberdoerffer

PMC · DOI: 10.1007/s10577-025-09789-9 · 2026-01-03

## TL;DR

This paper introduces a method to visualize DNA repair processes at transcription sites in single cells.

## Contribution

A novel visualization method for monitoring DNA repair during transcription-associated stress is presented.

## Key findings

- A reporter system detects nascent transcripts using MS2-repeat and YFP-tagged MS2 coat protein.
- The method allows monitoring Topoisomerase 1 engagement and TOP1 cleavage complex formation.
- The system enables visualization of DNA repair factor recruitment in response to transcription stress.

## Abstract

Transcription-associated torsional stress presents a continuous threat to genome integrity that needs to be tightly controlled. Here we present a method for the visualization of genome maintenance events at sites of active transcription, which builds on a previously developed reporter system that allows for the detection of nascent, MS2-repeat containing transcripts with a YFP-tagged MS2 coat protein. We describe steps to monitor Topoisomerase 1 engagement as a result of transcription-associated topological stress in both S phase and non-S phase cells, and detail procedures to visualize TOP1 cleavage complex formation and concomitant DNA repair factor engagement. We expect this system to provide a powerful means to study effectors of the transcription-associated topological stress response.

The online version contains supplementary material available at 10.1007/s10577-025-09789-9.

## Linked entities

- **Proteins:** TOP1ALPHA (DNA topoisomerase I alpha)

## Full-text entities

- **Genes:** TOP1 (DNA topoisomerase I) [NCBI Gene 7150] {aka TOPI}

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12764657/full.md

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Source: https://tomesphere.com/paper/PMC12764657