Sequence-specific detection of PCR-amplified DNA by restriction enzyme release of hybrids

Mol Cell Probes. 1996 Jun;10(3):179-85. doi: 10.1006/mcpr.1996.0025.

Abstract

We have developed a method to detect PCR amplicons that contain a restriction enzyme site. The method is called Polymerase Chain Reaction-Hybridization and Enzymatic Release Assay (PCR-HERA). The PCR product is hybridized to a synthetic oligonucleotide that is immobilized on a microtitre plate. Specific cleavage of the resulting hybrid by a restriction endonuclease liberates a fluorescein labeled arm of the immobilized DNA. We demonstrate the use of PCR-HERA to detect species-specific sequences of extra-chromosomal, ribosomal DNA, of Entamoeba histolytica. This highly specific assay does not require any washing steps and can be easily automated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • DNA Restriction Enzymes / analysis*
  • DNA, Protozoan / analysis
  • DNA, Ribosomal / analysis
  • DNA, Ribosomal / genetics
  • Entamoeba histolytica / genetics
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Polymerase Chain Reaction / methods*
  • Repetitive Sequences, Nucleic Acid

Substances

  • DNA, Protozoan
  • DNA, Ribosomal
  • DNA Restriction Enzymes