Reverse transcriptase-associated ribonuclease H does not require zinc for catalysis

J Biol Chem. 1979 Jun 10;254(11):4756-9.

Abstract

omicron-Phenanthroline, a zinc chelating agent, is known to inhibit the DNA polymerase activity of cellular DNA-dependent and viral RNA-dependent DNA polymerases. We find that omicron-phenanthroline does not inhibit the reverse transcriptase-associated RNase H activity of retroviruses. Kinetic studies, using DNA template-primers as an inhibitor of RNase H, suggest that zinc does not play any role in template-primer binding by reverse transcriptase. These results also indicate a distinct binding site for the template and triphosphate substrates. Cellular RNase H from calf thymus and RNase H-II from Rauscher leukemia virus are likewise resistant to omicron-phenanthroline inhibition, implying non-involvement of zinc in the nucleic acid hydrolysis by these enzymes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Avian Myeloblastosis Virus / metabolism
  • DNA-Directed DNA Polymerase / metabolism
  • Endonucleases / metabolism*
  • Kinetics
  • Oncogenic Viruses / enzymology
  • Phenanthrolines / pharmacology
  • RNA-Directed DNA Polymerase / metabolism*
  • Ribonucleases / metabolism*
  • Zinc / pharmacology*

Substances

  • Phenanthrolines
  • RNA-Directed DNA Polymerase
  • DNA-Directed DNA Polymerase
  • Endonucleases
  • Ribonucleases
  • Zinc