Directionality of DNA replication fork movement strongly affects the generation of spontaneous mutations in Escherichia coli

J Mol Biol. 2001 Apr 13;307(5):1195-206. doi: 10.1006/jmbi.2001.4557.

Abstract

Using a pair of plasmids carrying the rpsL target sequence in different orientations to the replication origin, we analyzed a large number of forward mutations generated in wild-type and mismatch-repair deficient (MMR(-)) Escherichia coli cells to assess the effects of directionality of replication-fork movement on spontaneous mutagenesis and the generation of replication error. All classes of the mutations found in wild-type cells but not MMR(-) cells were strongly affected by the directionality of replication fork movement. It also appeared that the directionality of replication-fork movement governs the directionality of sequence substitution mutagenesis, which occurred in wild-type cells at a frequency comparable to base substitutions and single-base frameshift mutations. A very strong orientation-dependent hot-spot site for single-base frameshift mutations was discovered and demonstrated to be caused by the same process involved in sequence substitution mutagenesis. It is surprising that dnaE173, a potent mutator mutation specific for sequence substitution as well as single-base frameshift, did not enhance the frequency of the hot-spot frameshift mutation. Furthermore, the frequency of the hot-spot frameshift mutation was unchanged in the MMR(-) strain, whereas the mutHLS-dependent mismatch repair system efficiently suppressed the generation of single-base frameshift mutations. These results suggested that the hot-spot frameshift mutagenesis might be initiated at a particular location containing a DNA lesion, and thereby produce a premutagenic replication intermediate resistant to MMR. Significant numbers of spontaneous single-base frameshift mutations are probably caused by similar mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Base Pair Mismatch / genetics
  • Base Sequence
  • DNA Mutational Analysis
  • DNA Polymerase III / genetics
  • DNA Polymerase III / metabolism
  • DNA Replication / genetics*
  • DNA-Binding Proteins*
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Escherichia coli Proteins*
  • Frameshift Mutation / genetics
  • Genes, Bacterial / genetics
  • Models, Genetic
  • Molecular Sequence Data
  • MutS DNA Mismatch-Binding Protein
  • Mutagenesis / genetics*
  • Plasmids / genetics
  • Point Mutation / genetics
  • Polymerase Chain Reaction
  • Ribosomal Protein S9

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • Ribosomal Protein S9
  • RpsI protein, E coli
  • DNA polymerase III, alpha subunit
  • DNA Polymerase III
  • Adenosine Triphosphatases
  • MutS DNA Mismatch-Binding Protein
  • MutS protein, E coli