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Updated: May 9, 2026

Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
Published on: June 8, 2018
Protocol for imaging-based quantification of RNAPII clearance during transcription-coupled DNA repair
Bram A F J de Groot1, Paula J van der Meer1, Diana van den Heuvel1
1Leiden University Medical Center (LUMC), Department of Human Genetics, Einthovenweg 20, 2333 ZC Leiden, the Netherlands.
Abstract:
Elongating RNA polymerase II (RNAPII) stalls at transcription-blocking lesions in the DNA template strand and is removed by transcription-coupled DNA repair (TCR) factors. Here, we present a protocol to measure RNAPII clearance during TCR at sites of localized UV-induced DNA damage in adherent cells. We describe how to induce local UV damage and visualize the damaged area and chromatin-bound RNAPII levels using immunofluorescence staining. This approach can quantify the clearance of DNA damage-stalled RNAPII and its dependence on TCR factors. For complete details on the use and execution of this protocol, please refer to van den Heuvel et al.1.
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