Transcriptional activation of ColE1 DNA synthesis by displacement of the nontranscribed strand

Cell. 1987 Dec 24;51(6):1123-30. doi: 10.1016/0092-8674(87)90598-8.

Abstract

Plasmid ColE1 can replicate using RNAase H and DNA polymerase I. However, it can also replicate in the absence of these enzymes. In this case, formation of a persistent hybrid between a transcript (RNA II) and the DNA indirectly activates subsequent DNA synthesis, instead of providing a primer as it does in the presence of these enzymes. To activate DNA synthesis, a certain length is required for the hybridized region and the region of minimum length cannot include a palindrome. These results show that the single-stranded region of DNA displaced by the hybridization is responsible for the activation. A single-stranded region was identified on the nontranscribed strand by its enhanced reactivity to dimethyl sulfate. The necessary length for the single-stranded region is at least 40 nucleotides. The region probably provides a site for initial binding of a helicase that further unwinds the template DNA for initiation of DNA synthesis.

MeSH terms

  • Bacterial Proteins / metabolism
  • Bacteriocin Plasmids*
  • Base Sequence
  • DNA Replication
  • DNA, Bacterial / biosynthesis*
  • DNA, Bacterial / metabolism
  • DNA, Single-Stranded / metabolism*
  • DNA-Binding Proteins / metabolism
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Models, Biological
  • Nucleic Acid Hybridization
  • Plasmids*
  • RNA, Bacterial / genetics
  • Templates, Genetic
  • Transcription, Genetic*

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • DNA, Single-Stranded
  • DNA-Binding Proteins
  • RNA, Bacterial