A mutant yeast topoisomerase II (top2G437S) with differential sensitivity to anticancer drugs in the presence and absence of ATP.

Abstract

To further characterize the mechanistic basis for cellular resistance/hypersensitivity to anticancer drugs, a yeast genetic system was used to select a mutant type II topoisomerase that conferred cellular resistance to CP-115,953, amsacrine, etoposide, and ellipticine. The mutant enzyme contained a single point mutation that converted Gly437 --> Ser (top2G437S). Purified top2G437S displayed wild-type enzymatic activity in the absence of drugs but exhibited two properties that were not predicted by the cellular resistance phenotype. First, in the absence of ATP, it was hypersensitive to all of the drugs examined and hypersensitivity correlated with increased drug affinity. Second, in the presence of ATP, top2G437S lost its hypersensitivity and displayed wild-type drug sensitivity. Since the resistance of yeast harboring top2G437S could not be explained by alterations in enzyme-drug interactions, physiological levels of topoisomerase II were determined. The Gly437 --> Ser mutation reduced the stability of topoisomerase II and decreased the cellular concentration of the enzyme. These findings suggest that the physiological drug resistance phenotype conferred by top2G437S results primarily from its decreased stability. This study highlights the need to analyze both the biochemistry and the physiology of topoisomerase II mutants with altered drug sensitivity in order to define the mechanistic bridge that links enzyme function to cellular phenotype.

• Authors: M Sabourin, J A Byl, S E Hannah, J L Nitiss, N Osheroff
• Journal: The Journal of biological chemistry (J Biol Chem) Vol. 273 Issue 44 Pg. 29086-92 (Oct 30 1998) ISSN: 0021-9258 [Print] United States
• PMID: 9786915 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antineoplastic Agents
• Serine
• Adenosine Triphosphate
• DNA Topoisomerases, Type II
• Glycine

Topics

• Adenosine Triphosphate (pharmacology)
• Antineoplastic Agents (pharmacology)
• DNA Topoisomerases, Type II (chemistry, drug effects, genetics)
• Drug Resistance, Neoplasm
• Enzyme Stability
• Glycine (genetics)
• Mutagenesis
• Saccharomyces cerevisiae (enzymology)
• Serine (genetics)