Folding transition of large DNA completely inhibits the action of a restriction endonuclease as revealed by single-chain observation

FEBS Lett. 2002 Oct 23;530(1-3):143-6. doi: 10.1016/s0014-5793(02)03448-8.

Abstract

The biochemical characteristics of lambda DNA chains in folded/unfolded states upon cleavage by the restriction enzyme ApaLI were investigated in the presence of spermine. These characteristics of DNA chains depending on their higher-order structure were studied at the single-molecule level using fluorescence microscopy. With a low concentration of spermine, lambda DNA takes a random coiled conformation and allows digestion by the enzyme, while under a high concentration of spermine, lambda DNA takes a compact folded structure and inhibits such attack. Together with comparative experiments on short oligomeric DNA, our results suggest that the transition in the higher-order structure causes on/off-type switching of sensitivity to the enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA / chemistry
  • DNA / metabolism*
  • DNA Restriction Enzymes / antagonists & inhibitors*
  • DNA Restriction Enzymes / metabolism
  • Nucleic Acid Conformation*
  • Spectrometry, Fluorescence
  • Spermine / metabolism

Substances

  • Spermine
  • DNA
  • DNA Restriction Enzymes