Interdependent progression of bidirectional sister replisomes in E. coli
Po Jui Chen,
Anna B McMullin,
Bryan J Visser,
Qian Mei,
Susan M Rosenberg,
David Bates
Affiliations
Po Jui Chen
Molecular Virology and Microbiology, Baylor College of Medicine, Houston, United States
Anna B McMullin
Molecular Virology and Microbiology, Baylor College of Medicine, Houston, United States
Bryan J Visser
Graduate Program in Integrative Molecular and Biomedical Sciences, Baylor College of Medicine, Houston, United States
Qian Mei
Systems, Synthetic, and Physical Biology Program, Rice University, Houston, United States
Susan M Rosenberg
Molecular Virology and Microbiology, Baylor College of Medicine, Houston, United States; Graduate Program in Integrative Molecular and Biomedical Sciences, Baylor College of Medicine, Houston, United States; Systems, Synthetic, and Physical Biology Program, Rice University, Houston, United States; Molecular and Human Genetics, Baylor College of Medicine, Houston, United States; Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, United States
Molecular Virology and Microbiology, Baylor College of Medicine, Houston, United States; Graduate Program in Integrative Molecular and Biomedical Sciences, Baylor College of Medicine, Houston, United States; Molecular and Human Genetics, Baylor College of Medicine, Houston, United States; Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, United States
Bidirectional DNA replication complexes initiated from the same origin remain colocalized in a factory configuration for part or all their lifetimes. However, there is little evidence that sister replisomes are functionally interdependent, and the consequence of factory replication is unknown. Here, we investigated the functional relationship between sister replisomes in Escherichia coli, which naturally exhibits both factory and solitary configurations in the same replication cycle. Using an inducible transcription factor roadblocking system, we found that blocking one replisome caused a significant decrease in overall progression and velocity of the sister replisome. Remarkably, progression was impaired only if the block occurred while sister replisomes were still in a factory configuration – blocking one fork had no significant effect on the other replisome when sister replisomes were physically separate. Disruption of factory replication also led to increased fork stalling and requirement of fork restart mechanisms. These results suggest that physical association between sister replisomes is important for establishing an efficient and uninterrupted replication program. We discuss the implications of our findings on mechanisms of replication factory structure and function, and cellular strategies of replicating problematic DNA such as highly transcribed segments.