Computational modeling of unphosphorylated CtrA:Cori binding in the Caulobacter cell cycle

iScience

John J. Tyson¹  Yang Cao²  Bronson R. Weston³ 

[1] Department of Biological Sciences, Virginia Tech, Blacksburg, VA, USA;Department of Computer Science, Virginia Tech, Blacksburg, VA, USA;Program in Genetics, Bioinformatics, and Computational Biology, Virginia Tech, Blacksburg, VA, USA;

关键词: Bacteriology;    In silico biology;    Mathematical biosciences;   

DOI  :  

来源: DOAJ

【 摘 要 】

Summary: In the alphaproteobacterium, Caulobacter crescentus, phosphorylated CtrA (CtrA∼P), a master regulatory protein, binds directly to the chromosome origin (Cori) to inhibit DNA replication. Using a mathematical model of CtrA binding at Cori site [d], we provide computational evidence that CtrAU can displace CtrA∼P from Cori at the G1-S transition. Investigation of this interaction within a detailed model of the C. crescentus cell cycle suggests that CckA phosphatase may clear Cori of CtrA∼P by altering the [CtrAU]/[CtrA∼P] ratio rather than by completely depleting CtrA∼P. Model analysis reveals that the mechanism allows for a speedier transition into S phase, stabilizes the timing of chromosome replication under fluctuating rates of CtrA proteolysis, and may contribute to the viability of numerous mutant strains. Overall, these results suggest that CtrAU enhances the robustness of chromosome replication. More generally, our proposed regulation of CtrA:Cori dynamics may represent a novel motif for molecular signaling in cell physiology.

【 授权许可】

Unknown