Ribonucleotide reductase and the regulation of DNA replication: an old story and an ancient heritage

Mol Microbiol. 2007 Jan;63(1):22-34. doi: 10.1111/j.1365-2958.2006.05493.x.

Abstract

All organisms that synthesize their own DNA have evolved mechanisms for maintaining a constant DNA/cell mass ratio independent of growth rate. The DNA/cell mass ratio is a central parameter in the processes controlling the cell cycle. The co-ordination of DNA replication with cell growth involves multiple levels of regulation. DNA synthesis is initiated at specific sites on the chromosome termed origins of replication, and proceeds bidirectionally to elongate and duplicate the chromosome. These two processes, initiation and elongation, therefore determine the total rate of DNA synthesis in the cell. In Escherichia coli, initiation depends on the DnaA protein while elongation depends on a multiprotein replication factory that incorporates deoxyribonucleotides (dNTPs) into the growing DNA chain. The enzyme ribonucleotide reductase (RNR) is universally responsible for synthesizing the necessary dNTPs. In this review we examine the role RNR plays in regulating the total rate of DNA synthesis in E. coli and, hence, in maintaining constant DNA/cell mass ratios during normal growth and under conditions of DNA stress.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • DNA Replication / physiology*
  • DNA, Bacterial / biosynthesis*
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Escherichia coli / growth & development
  • Gene Expression Regulation, Bacterial / physiology
  • Ribonucleotide Reductases / metabolism*

Substances

  • DNA, Bacterial
  • Ribonucleotide Reductases