Visualizing DNA repair factor recruitment at sites of transcription in single cells
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.
Authors
- Tae-Hee Lee (ORCID: https://orcid.org/0000-0002-6263-6499)
- Philipp Oberdoerffer (ORCID: https://orcid.org/0000-0002-2484-1440)
- Yubo Shi (ORCID: https://orcid.org/0000-0002-4005-2943)
- Tianyi Guan
Institutions
- Johns Hopkins University (US)
- University of Illinois Urbana-Champaign (US)
- Johns Hopkins Medicine (US)
Publication Details
- Journal
- Chromosome Research
- Published
- 2026-01-03
- DOI
- https://doi.org/10.1007/s10577-025-09789-9
- Primary Topic
- DNA Repair Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Pennsylvania
- Johns Hopkins University
- National Institutes of Health