Conservation of organization in the specificity polypeptides of two families of type I restriction enzymes

J Mol Biol. 1989 Oct 5;209(3):335-44. doi: 10.1016/0022-2836(89)90001-6.

Abstract

We have identified the recognition sequence for the Citrobacter freundii restriction endonuclease CfrA, a member of the A-family of type I R-M enzymes. This bipartite target sequence differs in both its components from those of other type I enzymes. We determined the nucleotide sequence of its specificity gene (hsdS) and a comparison of this with its relative EcoA identifies two extensive variable regions, an organization analogous to that found in the K-family of type I R-M enzymes. The specificity polypeptides of the A-family, unlike those of K, have an N-terminal conserved region, and this includes a sequence repeated within the central conserved region. A second repeat sequence, identified at the amino acid level, coincides with the only sequence similarity common to all type I S polypeptides. Sequences immediately downstream from the hsdS genes of EcoA, CfrA, EcoK, B and D are almost identical, consistent with an allelic chromosomal location.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Citrobacter / enzymology*
  • Codon
  • DNA, Bacterial
  • Deoxyribonucleases, Type I Site-Specific / genetics*
  • Genes, Bacterial
  • Molecular Sequence Data
  • Peptides / genetics*
  • Repetitive Sequences, Nucleic Acid

Substances

  • Codon
  • DNA, Bacterial
  • Peptides
  • endodeoxyribonuclease CfrA
  • Deoxyribonucleases, Type I Site-Specific