Unscheduled DNA synthesis induced by N-methyl-N'-nitro-N-nitrosoguanidine in Hela cells

Gan. 1982 Feb;73(1):63-9.

Abstract

N-Methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced repair (unscheduled) DNA synthesis was studied in intact HeLa cells as well as in the cell lysate. The incorporation of dTTP[methyl-3H] in vitro by the cell lysate was dependent on the dose of MNNG, and as linear for 2 min, reaching the maximum at 4 min. The optimum conditions were the same as for UV-induced in vitro repair synthesis. The presence of hydroxyurea and arabinofuranosyl cytosine during in vivo incubation with MNNG was necessary for enhancement of in vitro DNA synthesis. This MNNG-induced in vitro DNA synthesis was inhibited by aphidicolin, but not by 2',3'-dideoxythymidine-5'-triphosphate. It thus appears that DNA polymerase alpha participates in MNNG-induced unscheduled DNA synthesis in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aphidicolin
  • Cytarabine / pharmacology
  • DNA / biosynthesis*
  • DNA Polymerase II / antagonists & inhibitors
  • Dideoxynucleotides
  • Diterpenes / pharmacology
  • HeLa Cells / drug effects
  • HeLa Cells / metabolism
  • Humans
  • Hydroxyurea / pharmacology
  • Methylnitronitrosoguanidine / pharmacology*
  • Nucleic Acid Synthesis Inhibitors*
  • Thymine Nucleotides / pharmacology

Substances

  • Dideoxynucleotides
  • Diterpenes
  • Nucleic Acid Synthesis Inhibitors
  • Thymine Nucleotides
  • Cytarabine
  • Methylnitronitrosoguanidine
  • Aphidicolin
  • DNA
  • DNA Polymerase II
  • 2',3'-dideoxythymidine triphosphate
  • Hydroxyurea