A mathematical model of ParA filament-mediated chromosome movement in Caulobacter crescentus.
نویسندگان
چکیده
Caulobacter crescentus uses the dynamic interactions between ParA and ParB proteins to segregate copies of its circular chromosome. In this paper, we develop two mathematical models of the movement of the circular chromosome of this bacterium during division. In the first model, posed as a set of stochastic differential equations (SDE), we propose that a simple biased diffusion mechanism for ParB/ParA interactions can reproduce the observed patterns of ParB and ParA localization in the cell. The second model, posed as a set of nonlinear partial differential equations, is a continuous treatment of the problem where we use results from the SDE model to describe ParB/ParA interactions and we also track ParA monomer dynamics in the cytoplasm. For both models, we show that if ParB complexes bind weakly and nonspecifically to ParA filaments, then they can closely track and move with the edge of a shrinking ParA filament bundle. Unidirectional chromosome movement occurs when ParB complexes have a passive role in depolymerizing ParA filaments. Finally, we show that tight control of ParA filament dynamics is essential for proper segregation.
منابع مشابه
Evidence for a DNA-relay mechanism in ParABS-mediated chromosome segregation
The widely conserved ParABS system plays a major role in bacterial chromosome segregation. How the components of this system work together to generate translocation force and directional motion remains uncertain. Here, we combine biochemical approaches, quantitative imaging and mathematical modeling to examine the mechanism by which ParA drives the translocation of the ParB/parS partition compl...
متن کاملProductive interaction between the chromosome partitioning proteins, ParA and ParB, is required for the progression of the cell cycle in Caulobacter crescentus.
In Caulobacter crescentus the partitioning proteins ParA and ParB operate a molecular switch that couples chromosome partitioning to cytokinesis. Homologues of these proteins have been shown to be important for the stable inheritance of F-plasmids and the prophage form of bacteriophage P1. In C. crescentus, ParB binds to sequences adjacent to the origin of replication and is required for the in...
متن کاملThe chromosome partitioning protein, ParB, is required for cytokinesis in Caulobacter crescentus.
In Caulobacter crescentus, the genes encoding the chromosome partitioning proteins, ParA and ParB, are essential. Depletion of ParB resulted in smooth filamentous cells in which DNA replication continued. Immunofluorescence microscopy revealed that the formation of FtsZ rings at the mid-cell, the earliest molecular event in the initiation of bacterial cell division, was blocked in cells lacking...
متن کاملFilament Depolymerization Can Explain Chromosome Pulling during Bacterial Mitosis
Chromosome segregation is fundamental to all cells, but the force-generating mechanisms underlying chromosome translocation in bacteria remain mysterious. Caulobacter crescentus utilizes a depolymerization-driven process in which a ParA protein structure elongates from the new cell pole, binds to a ParB-decorated chromosome, and then retracts via disassembly, pulling the chromosome across the c...
متن کاملA family of six flagellin genes contributes to the Caulobacter crescentus flagellar filament.
The Caulobacter crescentus flagellar filament is assembled from multiple flagellin proteins that are encoded by six genes. The amino acid sequences of the FljJ and FljL flagellins are divergent from those of the other four flagellins. Since these flagellins are the first to be assembled in the flagellar filament, one or both might have specialized to facilitate the initiation of filament assembly.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Journal of theoretical biology
دوره 307 شماره
صفحات -
تاریخ انتشار 2012