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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

RNA polymerase II is a polar roadblock to a progressing DNA fork

Dirk Remus, Michelle D. Wang, Lucyna Lubkowska, James T. Inman et al.
4 citations
Nature Communications
DNA Repair Mechanisms
3.22
article

RNA polymerase II is a polar roadblock to a progressing DNA fork

Dirk Remus, Michelle D. Wang, Lucyna Lubkowska, James T. Inman, Porter M. Hall, Sahil Batra, Tung T. Le, Mikhail Kashlev, Dong Wang, Jin Qian, Teresa Kay
article en
4 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
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)
National Institutes of Health, National Cancer Institute
Openalex Percentile: Top 7%
DNA Repair Mechanisms
3.22
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.