In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli

Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):783-7. doi: 10.1073/pnas.92.3.783.

Abstract

In vitro, anionic phospholipids can reactivate inactivated DnaA protein, which is essential for initiation of DNA replication at the oriC site of Escherichia coli [Sekimizu, K. & Kornberg, A. (1988) J. Biol. Chem. 263, 7131-7135]. Mutations in the pgsA gene (encoding phosphatidylglycerophosphate synthase) limit the synthesis of the major anionic phospholipids and lead to arrest of cell growth. We report herein that a mutation in the rnhA gene (encoding RNase H) that bypasses the need for the DnaA protein through induction of constitutive stable DNA replication [Kogoma, T. & von Meyenburg, K. (1983) EMBO J. 2, 463-468] also suppressed the growth arrest phenotype of a pgsA mutant. The maintenance of plasmids dependent on an oriC site for replication, and therefore DnaA protein, was also compromised under conditions of limiting anionic phospholipid synthesis. These results provide support for the involvement of anionic phospholipids in normal initiation of DNA replication at oriC in vivo by the DnaA protein.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anions
  • Bacterial Proteins / physiology
  • DNA Replication / physiology*
  • DNA-Binding Proteins / physiology
  • Escherichia coli / genetics*
  • Escherichia coli / physiology
  • Genes, Bacterial / genetics
  • Models, Genetic*
  • Mutation / physiology
  • Phospholipids / chemistry
  • Phospholipids / physiology*
  • Phosphotransferases / metabolism
  • Phosphotransferases / physiology
  • Plasmids / biosynthesis
  • Replication Origin / physiology
  • Ribonuclease H / genetics
  • Suppression, Genetic

Substances

  • Anions
  • Bacterial Proteins
  • DNA-Binding Proteins
  • DnaA protein, Bacteria
  • Phospholipids
  • Phosphotransferases
  • Ribonuclease H