The nature of the deoxyribonucleosides involved in the binding of carcinogenic hydrocarbons to the DNA of mouse embryo cells

Int J Cancer. 1975 Jun 15;15(6):912-7. doi: 10.1002/ijc.2910150606.

Abstract

The DNA of mouse embryo cells was specifically labelled in the purine moieties with (G(3)H)-deoxyadenosine or in the cytosine moieties with (5-(3)H)-deoxycytidine. These cells were then treated with 7-methylbenz (a) anthracene (7MBA) or benzo (a)-pyrene (B(a)P) and the DNA isolated, degraded and fractionated by LH20 Sephadex column chromatography. When the purines of the DNA were tritium-labelled, radioactive hydroccarbondeoxyribonucleoside products were obtained. No such products were found with deoxycytidine pre-labelled DNA. Contrary to an earlier suggestion, these results indicate that it is the purine moieties of DNA which react with the metabolically activated hydrocarbon derivative in vivo.

Publication types

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

MeSH terms

  • Animals
  • Benz(a)Anthracenes / metabolism
  • Benzopyrenes / metabolism
  • Binding Sites
  • Carcinogens / metabolism*
  • Cells, Cultured
  • DNA / metabolism*
  • Deoxyadenosines / metabolism
  • Deoxycytidine / pharmacology
  • Deoxyribonucleosides / metabolism*
  • Embryo, Mammalian
  • Hydrocarbons / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Purines / metabolism

Substances

  • Benz(a)Anthracenes
  • Benzopyrenes
  • Carcinogens
  • Deoxyadenosines
  • Deoxyribonucleosides
  • Hydrocarbons
  • Purines
  • Deoxycytidine
  • DNA