Evidence for a mutant allele of the gene for DNA topoisomerase II in adriamycin-resistant P388 murine leukemia cells

Cancer Res. 1989 Dec 15;49(24 Pt 1):6879-82.

Abstract

Previous studies have shown that DNA topoisomerase II enzyme activity and protein levels are reduced in cloned lines of Adriamycin-resistant P388 leukemia cells relative to drug-sensitive cells (Deffie et al., Cancer Res., 49: 58-62, 1989). The molecular basis of the reduced topoisomerase II levels in these resistant cells has been investigated. Northern blot analysis of total cellular RNA from drug-sensitive and -resistant cells using a 1.8-kilobase human topoisomerase II complementary DNA revealed the presence of two mRNA species: a 6.6-kilobase transcript that was strongly expressed in drug-sensitive cells but reduced 7- to 8-fold in resistant cells; and a 5.5-kilobase transcript detected only in drug-resistant cells. Southern blot analysis of genomic DNA digested with BamHI, StuI, or PvuII and probed with the 1.8-kilobase complementary DNA for human topoisomerase II showed that, in Adriamycin-resistant cells, there were two different alleles for topoisomerase II, one identical to the native allele but with a lower gene copy number than that found in sensitive cells, and a second allele containing a mutation present only in resistant cells. These findings suggest that the reduced levels of topo II protein in drug-resistant cells may be due to reduced amounts of the native 6.6-kilobase mRNA. The unique 5.5-kilobase mRNA in resistant cells may represent a shortened transcript of the mutated topoisomerase II allele.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Animals
  • Blotting, Northern
  • Blotting, Southern
  • DNA / genetics
  • DNA Probes
  • DNA Topoisomerases, Type II / genetics*
  • DNA, Neoplasm / genetics
  • Doxorubicin / pharmacology*
  • Drug Resistance
  • Leukemia P388 / enzymology
  • Leukemia P388 / genetics*
  • Leukemia, Experimental / genetics*
  • Mice
  • Mutation*
  • RNA, Neoplasm / genetics
  • Tumor Cells, Cultured

Substances

  • DNA Probes
  • DNA, Neoplasm
  • RNA, Neoplasm
  • Doxorubicin
  • DNA
  • DNA Topoisomerases, Type II