Modeling the 3D Spatiotemporal Organization of Chromatin Replication

We propose a polymer model to investigate the dynamics of chromatin replication in three dimensions (PolyRep). Our results indicate that replication complexes, the replisomes, may self-assemble during the process and replicate chromatin by extruding it (immobile replisome) or by moving along the template filament (tracking replisome), reconciling previous discordant experimental evidence in favour of either scenario. Importantly, the emergence of one of the two morphologies depends in a major way on the replication origin distribution as well as on the presence of nonspecific interactions between unreplicated chromatin and firing factors—polymerases and other components of the replisome. Nonspecific interactions also appear instrumental to creating clusters of factors and replication forks, structures akin to the replication foci observed in mammalian cells . PolyRep simulations predict different mechanisms for foci evolution, including unanticipated loop-mediated fusion dynamics. We suggest that cluster formation, which our model suggests to be a generic feature of chromatin replication, provides a hitherto underappreciated but robust pathway to avoid stalled or faulty forks, which would otherwise diminish the efficiency of the replication process. Published by the American Physical Society 2024

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Publication Details

Journal
PRX Life
Published
2024-09-26
DOI
https://doi.org/10.1103/prxlife.2.033014
Citations
11
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
2.57

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article

Modeling the 3D Spatiotemporal Organization of Chromatin Replication

Davide Marenduzzo, Sara B.C. Buonomo, Giada Forte, Peter R. Cook et al.
11 citations
PRX Life
Genomics and Chromatin Dynamics
2.57
article

Modeling the 3D Spatiotemporal Organization of Chromatin Replication

Davide Marenduzzo, Sara B.C. Buonomo, Giada Forte, Peter R. Cook, Nick Gilbert, Enzo Orlandini
article en
11 citations

Abstract

We propose a polymer model to investigate the dynamics of chromatin replication in three dimensions (PolyRep). Our results indicate that replication complexes, the replisomes, may self-assemble during the process and replicate chromatin by extruding it (immobile replisome) or by moving along the template filament (tracking replisome), reconciling previous discordant experimental evidence in favour of either scenario. Importantly, the emergence of one of the two morphologies depends in a major way on the replication origin distribution as well as on the presence of nonspecific interactions between unreplicated chromatin and firing factors—polymerases and other components of the replisome. Nonspecific interactions also appear instrumental to creating clusters of factors and replication forks, structures akin to the replication foci observed in mammalian cells . PolyRep simulations predict different mechanisms for foci evolution, including unanticipated loop-mediated fusion dynamics. We suggest that cluster formation, which our model suggests to be a generic feature of chromatin replication, provides a hitherto underappreciated but robust pathway to avoid stalled or faulty forks, which would otherwise diminish the efficiency of the replication process. Published by the American Physical Society 2024

PRX LifeVol. 2(3)
University of Padua (IT), University of Oxford (GB), University of Edinburgh (GB)
Wellcome Trust, Agenzia Nazionale di Valutazione del Sistema Universitario e della Ricerca
Openalex Percentile: Top 10%
Genomics and Chromatin Dynamics
2.57
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