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Dynamics of chromosome organization in a minimal bacterial cell.
Gilbert, Benjamin R; Thornburg, Zane R; Brier, Troy A; Stevens, Jan A; Grünewald, Fabian; Stone, John E; Marrink, Siewert J; Luthey-Schulten, Zaida.
Affiliation
  • Gilbert BR; Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, United States.
  • Thornburg ZR; Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, United States.
  • Brier TA; Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, United States.
  • Stevens JA; Molecular Dynamics Group, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, Netherlands.
  • Grünewald F; Molecular Dynamics Group, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, Netherlands.
  • Stone JE; NVIDIA Corporation, Santa Clara, CA, United States.
  • Marrink SJ; NIH Center for Macromolecular Modeling and Bioinformatics, Beckman Institute, University of Illinois at Urbana-Champaign, Urbana, IL, United States.
  • Luthey-Schulten Z; Molecular Dynamics Group, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, Netherlands.
Front Cell Dev Biol ; 11: 1214962, 2023.
Article in En | MEDLINE | ID: mdl-37621774
ABSTRACT
Computational models of cells cannot be considered complete unless they include the most fundamental process of life, the replication and inheritance of genetic material. By creating a computational framework to model systems of replicating bacterial chromosomes as polymers at 10 bp resolution with Brownian dynamics, we investigate changes in chromosome organization during replication and extend the applicability of an existing whole-cell model (WCM) for a genetically minimal bacterium, JCVI-syn3A, to the entire cell-cycle. To achieve cell-scale chromosome structures that are realistic, we model the chromosome as a self-avoiding homopolymer with bending and torsional stiffnesses that capture the essential mechanical properties of dsDNA in Syn3A. In addition, the conformations of the circular DNA must avoid overlapping with ribosomes identitied in cryo-electron tomograms. While Syn3A lacks the complex regulatory systems known to orchestrate chromosome segregation in other bacteria, its minimized genome retains essential loop-extruding structural maintenance of chromosomes (SMC) protein complexes (SMC-scpAB) and topoisomerases. Through implementing the effects of these proteins in our simulations of replicating chromosomes, we find that they alone are sufficient for simultaneous chromosome segregation across all generations within nested theta structures. This supports previous studies suggesting loop-extrusion serves as a near-universal mechanism for chromosome organization within bacterial and eukaryotic cells. Furthermore, we analyze ribosome diffusion under the influence of the chromosome and calculate in silico chromosome contact maps that capture inter-daughter interactions. Finally, we present a methodology to map the polymer model of the chromosome to a Martini coarse-grained representation to prepare molecular dynamics models of entire Syn3A cells, which serves as an ultimate means of validation for cell states predicted by the WCM.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Cell Dev Biol Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Cell Dev Biol Year: 2023 Type: Article Affiliation country: United States