Semi-conservative replication in yeast nuclear extracts requires Dna2 helicase and supercoiled template

J Mol Biol. 1998 Aug 28;281(4):631-49. doi: 10.1006/jmbi.1998.1973.

Abstract

We describe the preparation of nuclear extracts from yeast cells synchronised in S-phase that support the aphidicolin-sensitive, semi-conservative replication of primer-free, supercoiled plasmid in vitro. This is monitored by one and two-dimensional gel electrophoresis of replication intermediates that have incorporated [alpha-32P]dATP, by the conversion of methylated template DNA into a hemi-methylated or DpnI-resistant form, and by substitution of dTTP with the heavy derivative BrdUTP, which results in a shift in density corresponding to complete second strand synthesis. We demonstrate dependence on DNA pol delta and the pol alpha/primase complex, and are able to detect putative Okazaki fragments under ATP-limiting conditions. In contrast to the semi-conservative replication of supercoiled plasmid, linear or open-circular templates incorporate labelled nucleotides through repair synthesis that produces no significant density shift on CsCl gradients. Consistent with a true replication reaction we find that semi-conservative replication of plasmid DNA is stimulated in S-phase relative to G1-phase nuclear extracts, and is independent of the recombination-promoting factor Rad52p. Using this novel system we demonstrate that semi-conservative replication, but not polymerase activity per se, requires the activity of the DNA helicase encoded by DNA2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / physiology*
  • Aphidicolin / pharmacology
  • Cell Cycle / physiology
  • Cell Nucleus / metabolism*
  • Centrifugation, Density Gradient
  • DNA Helicases*
  • DNA Methylation
  • DNA Polymerase I / metabolism
  • DNA Polymerase III / metabolism
  • DNA Replication / genetics*
  • DNA, Superhelical / metabolism*
  • DNA, Superhelical / ultrastructure
  • Deoxyadenine Nucleotides / metabolism
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Deoxyuracil Nucleotides / metabolism
  • Electrophoresis, Gel, Two-Dimensional
  • Microscopy, Electron
  • Nuclear Proteins / metabolism
  • Nucleic Acid Conformation
  • Plasmids / genetics
  • Plasmids / ultrastructure
  • RNA / metabolism
  • Saccharomyces cerevisiae / enzymology*

Substances

  • DNA, Superhelical
  • Deoxyadenine Nucleotides
  • Deoxyuracil Nucleotides
  • Nuclear Proteins
  • bromodeoxyuridine triphosphate
  • Aphidicolin
  • RNA
  • DNA Polymerase I
  • DNA Polymerase III
  • endodeoxyribonuclease DpnI
  • Deoxyribonucleases, Type II Site-Specific
  • Adenosine Triphosphatases
  • DNA Helicases
  • 2'-deoxyadenosine triphosphate