The mechanism and driving forces of chromosome segregation in the bacterial cell cycle of E. coli is one of the least understood events in its life cycle [1,2,3]. Using principles of entropic repulsion between DNA-polymer loops confined in a cylinder, we use Monte carlo simulations to show that the segregation is spontaneously enhanced by the adoption of a certain DNA-polymer architecture as replication progresses. Secondly, the chosen polymer-topology ensures its self-organization along the cell axis while segregation is in progress, such that various chromosomal segments (loci) get spatially localized as seen in-vivo [4]. The evolution of loci positions match the corresponding experimentally reported results for E.coli using FISH [5]. Additionally, the contact map generated using our bead-spring model [4] reproduces the four macrodomains of the experimental Hi-C maps [6]. We modify the architecture by adding just four crosslinks at specific positions along the chain contour in 500 monomer bead- spring ring polymer, which represents the choromosome. After replication of our model-polymer, we obtain two 500-monomer ring polymers, which spontaneously get segregated and organized by virtue of their polymer topology. Thus we have proposed a framework which reconciles many spatial organizational aspects of E. coli chromosome as seen in-vivo, and provides a consistent mechanistic understanding of the process underlying segregation. Certain proteins are expected to contribute to change the DNA-polymer architecture. We also observe quantitative match of FISH data [7] and HiC data [3] for another bacteria C.crescentus where we use another polymer topology [8]. We have extended our studies to investigate chromosome organization in fast growth conditions for E.coli [9]. We have investigated a host of polymer topologies to develop understanding of how polymer topologies effect organization and segregation forces in cylindrical confinement.
References