Tuning the replication fork progression by the initiation frequency.

Environ Microbiol

Departmento de Bioquímica Biología Molecular y Genética, Universidad de Extremadura, 06071, Badajoz, Spain.

Published: December 2013

AI Article Synopsis

  • The thermo-sensitive ribonucleotide reductase RNR101 in E. coli, associated with the nrdA101 allele, shows a prolonged thermo-resistant period at 42°C, leading to a 45% increase in DNA content.
  • Impaired fork progression in the nrdA101 mutant suggests that fewer replication rounds and a drop in the oriC/terC ratio at 30°C may improve thermo-resistance by avoiding detrimental effects on cell division and viability at higher temperatures.
  • The findings indicate that the relationship between replication initiation frequency and fork progression is critical for efficient cell cycle regulation, potentially impacting replication processes in various systems.

Article Abstract

The thermo-resistant period of the thermo-sensitive ribonucleotide reductase RNR101 encoded by the nrdA101 allele in Escherichia coli is prolonged for 50 min at 42°C, enabling an increase in DNA content of about 45%. Assuming that fork progression in the nrdA101 mutant is impaired, the question whether reduced number of ongoing replication rounds altered the thermo-resistant period in this strain was investigated. Decreases in the oriC/terC ratio and in the number of oriC per cell at 30°C were found in the presence of oriC228, oriC229 and oriC239 alleles in strain nrdA101. Correlated with this effect, increased thermo-resistance period of the RNR101 was allowed, and the detrimental effects on cell division, chromosome segregation and cell viability observed in the nrdA101 mutant at 42°C were suppressed. These results indicate that conditions leading to chromosome initiation deficiency at 30°C enhance the replication fork progression in the nrdA101 mutant at 42°C. We propose that coordination between initiation frequency and replication fork progression could be significant for most of the replication systems with important consequences in their cell cycle regulation.

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http://dx.doi.org/10.1111/1462-2920.12127DOI Listing

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