Dynamic anatomy of the replisome under stress
Schulte, L.; Pabba, M. K.; Kamkaew, M.; Prorok, P.; Arroyo, M.; Cardoso, M. C.
Show abstract
When exposed to replication stress, the factors involved in DNA replication display differing responses that in many cases remain unexplained. In this study, we generated a series of genomically engineered embryonic stem cell lines with fluorescently tagged replication factors to track their spatiotemporal dynamics in live-cell microscopy during and after treatment with the replication inhibitors aphidicolin and hydroxyurea. All 3 replicative polymerases were found to accumulate upon stress, with the primase subunits of polymerase alpha retaining catalytic activity. This accumulation was dependent on new origin firing and accompanied by 9-1-1 clamp loading in the vicinity of stalled forks. Pulse-stress-pulse experiments and spatial correlation analyses of replicons indicated that, after stress is removed, replication preferentially restarts at new sites surrounding previously stalled forks. These findings shed light on the replisomes immediate reaction to stalled replication forks and provide comprehensive kinetic maps of the replisome under stress. Highlights- Comprehensible atlas of the replisome under stress - DNA polymerases accumulate during stress, with clamp switch near stalled forks - In the absence of DNA synthesis, new adjacent origins fire with active priming - During stress recovery, replication restart predominantly at new fired origins
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Replisome loading reduces chromatin motion independent of DNA synthesis 98%
- Treacle's ability to form liquid-like phase condensates is essential for nucleolar fibrillar center assembly, efficient rRNA transcription and processing, and rRNA gene repair 96%
- Role of BRCA2 DNA-binding and C-terminal domain on its mobility and conformation in DNA repair 96%
Similar papers in this journal
- Cohesin-mediated DNA loop extrusion resolves sister chromatids in G2 phase 97%
- Cold induced chromatin compaction and nuclear retention of clock mRNAs resets the circadian rhythm 96%
- Human CST complex protects replication fork stability by directly blocking MRE11 degradation of nascent strand DNA 96%
Similar papers in this journal
- Suppression of liquid-liquid phase separation by 1,6-hexanediol partially compromises the 3D genome organization in living cells 96%
- The Consequences of Differential Origin Licensing Dynamics in Distinct Chromatin Environments 96%
- Human DNA replication initiation sites are specified epigenetically by oxidation of 5-methyl-deoxycytidine 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.