ParABS system induces topological modifications to spatio-temporally organize its mother and daughter chromosomes in the replicating C. crescentus cell
Abstract
We identify an entropy-mediated mechanism underlying the spatiotemporal organization of the chromosome in the bacterial cell Caulobacter crescentus. Effective entropic interactions between replicating DNA segments emerge from their topological modifications of daughter DNA polymers caused by transient ParA-ParB binding. Enthalpic contributions arising from the ParABS system further influence their dynamics. In C. crescentus, chromosome replication and segregation occur concurrently before cell division. The origin of replication oriC of the mother chromosome of C. crescentus is tethered to the old cell pole. Replication generates two daughter oriCs, one of which remains anchored at the old pole. The other oriC is actively transported toward the new pole by the ParABS system of proteins even as replication of the rest of the chain is in progress. How ParABS generates a directed force to transport a daughter oriC to the opposite pole during chromosome replication remains unclear. Furthermore, the two daughter chromosomes get neatly segregated into two halves of the cell. In a bead-spring polymer model of the replicating C. crescentus chromosome, we model transient ParA-ParB contacts that generate DNA loops and an effective entropic repulsion. This repulsion drives chromosome segregation and produces oriC trajectories consistent with experiments, aided by the ParA concentration gradient near the new pole. This minimal framework, incorporating the physics of topologically modified (ToMo) polymers, allows us to quantitatively reproduce the time-dependent spatial organization of different tagged loci and replisomes observed in multiple experiments. Incorporating a minimal model of extrusion also allows us to recover the linear arrangement of the chromosome arms, as is inferred from the characteristic diagonals of Hi-C maps.
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BibTeX
@misc{sathe2026parabs,
title = {{ParABS system induces topological modifications to spatio-temporally organize its mother and daughter chromosomes in the replicating C. crescentus cell}},
author = {Shailesh Sathe and Apratim Chatterji},
howpublished = {arXiv},
year = {2026},
month = oct,
doi = {10.48550/arxiv.2610.03118},
eprint = {2610.03118},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2610.03118},
note = {CC BY-NC-SA 4.0},
}
RIS
TY - UNPB
TI - ParABS system induces topological modifications to spatio-temporally organize its mother and daughter chromosomes in the replicating C. crescentus cell
AU - Shailesh Sathe
AU - Apratim Chatterji
PY - 2026
DA - 2026/10/02
PB - arXiv
DO - 10.48550/arxiv.2610.03118
UR - https://arxiv.org/abs/2610.03118
AB - We identify an entropy-mediated mechanism underlying the spatiotemporal organization of the chromosome in the bacterial cell Caulobacter crescentus. Effective entropic interactions between replicating DNA segments emerge from their topological modifications of daughter DNA polymers caused by transient ParA-ParB binding. Enthalpic contributions arising from the ParABS system further influence their dynamics. In C. crescentus, chromosome replication and segregation occur concurrently before cell division. The origin of replication oriC of the mother chromosome of C. crescentus is tethered to the old cell pole. Replication generates two daughter oriCs, one of which remains anchored at the old pole. The other oriC is actively transported toward the new pole by the ParABS system of proteins even as replication of the rest of the chain is in progress. How ParABS generates a directed force to transport a daughter oriC to the opposite pole during chromosome replication remains unclear. Furthermore, the two daughter chromosomes get neatly segregated into two halves of the cell. In a bead-spring polymer model of the replicating C. crescentus chromosome, we model transient ParA-ParB contacts that generate DNA loops and an effective entropic repulsion. This repulsion drives chromosome segregation and produces oriC trajectories consistent with experiments, aided by the ParA concentration gradient near the new pole. This minimal framework, incorporating the physics of topologically modified (ToMo) polymers, allows us to quantitatively reproduce the time-dependent spatial organization of different tagged loci and replisomes observed in multiple experiments. Incorporating a minimal model of extrusion also allows us to recover the linear arrangement of the chromosome arms, as is inferred from the characteristic diagonals of Hi-C maps.
ER -