RNA polymerase II is a polar roadblock to a progressing DNA fork
Transcription-replication conflicts threaten genome stability. Although head-on conflicts are more detrimental and prone to R-loop formation than co-directional conflicts, the cause of this RNA polymerase roadblock polarity remains unclear, and proposed structures of these R-loops are speculative. Here, we examine the Pol II roadblock to a DNA fork advanced by mechanical unzipping to mimic replisome progression. We found that a head-on Pol II with a minimal transcript resists disruption more strongly, revealing inherent polarity. Moreover, an elongating Pol II with a long RNA transcript becomes an even more potent roadblock, mediated by RNA-DNA hybrid formation. Surprisingly, when a Pol II collides with the DNA fork head-on and becomes backtracked, a hybrid can form in front of Pol II, creating a topological lock that traps Pol II at the fork. Our findings capture the basal properties of Pol II interactions with a DNA fork, revealing significant implications for transcription-replication conflicts.
Authors
- Dirk Remus (ORCID: https://orcid.org/0000-0002-5155-181X)
- Michelle D. Wang (ORCID: https://orcid.org/0000-0001-9137-3790)
- Lucyna Lubkowska
- James T. Inman (ORCID: https://orcid.org/0000-0003-3534-0323)
- Porter M. Hall (ORCID: https://orcid.org/0000-0001-5403-719X)
- Sahil Batra (ORCID: https://orcid.org/0000-0003-4210-3991)
- Tung T. Le (ORCID: https://orcid.org/0000-0002-5481-4080)
- Mikhail Kashlev (ORCID: https://orcid.org/0000-0002-1260-6486)
- Dong Wang (ORCID: https://orcid.org/0000-0002-2829-1546)
- Jin Qian (ORCID: https://orcid.org/0009-0001-0034-0246)
- Teresa Kay (ORCID: https://orcid.org/0000-0003-3622-2281)
Institutions
- Memorial Sloan Kettering Cancer Center (US)
- Howard Hughes Medical Institute (US)
- Cornell University (US)
- University of California San Diego (US)
- National Cancer Institute (US)
- Center for Cancer Research (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-09-29
- DOI
- https://doi.org/10.1038/s41467-025-63662-1
- Citations
- 4
- Primary Topic
- DNA Repair Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 3.22
Funders
- National Institutes of Health
- National Cancer Institute