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Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target.

Publication ,  Journal Article
Del Poeta, M; Toffaletti, DL; Rude, TH; Dykstra, CC; Heitman, J; Perfect, JR
Published in: Genetics
May 1999

Topisomerase I is the target of several toxins and chemotherapy agents, and the enzyme is essential for viability in some organisms, including mice and drosophila. We have cloned the TOP1 gene encoding topoisomerase I from the opportunistic fungal pathogen Cryptococcus neoformans. The C. neoformans topoisomerase I contains a fungal insert also found in topoisomerase I from Candida albicans and Saccharomyces cerevisiae that is not present in the mammalian enzyme. We were unable to disrupt the topoisomerase I gene in this haploid organism by homologous recombination in over 8000 transformants analyzed. When a second functional copy of the TOP1 gene was introduced into the genome, the topoisomerase I gene could be readily disrupted by homologous recombination (at 7% efficiency). Thus, topoisomerase I is essential in C. neoformans. This new molecular strategy with C. neoformans may also be useful in identifying essential genes in other pathogenic fungi. To address the physiological and pathobiological functions of the enzyme, the TOP1 gene was fused to the GAL7 gene promoter. The resulting GAL7::TOP1 fusion gene was modestly regulated by carbon source in a serotype A strain of C. neoformans. Modest overexpression of topoisomerase I conferred sensitivity to heat shock, gamma-rays, and camptothecin. In contrast, alterations in topoisomerase I levels had no effect on the toxicity of a novel class of antifungal agents, the dicationic aromatic compounds (DACs), indicating that topoisomerase I is not the target of DACs. In an animal model of cryptococcal meningitis, topoisomerase I regulation was not critically important to established infection, but may impact on the initial stress response to infection. In summary, our studies reveal that topoisomerase I is essential in the human pathogen C. neoformans and represents a novel target for antifungal agents.

Duke Scholars

Published In

Genetics

DOI

ISSN

0016-6731

Publication Date

May 1999

Volume

152

Issue

1

Start / End Page

167 / 178

Location

United States

Related Subject Headings

  • Time Factors
  • Sequence Homology, Amino Acid
  • Reverse Transcriptase Polymerase Chain Reaction
  • Radiation, Ionizing
  • Rabbits
  • Plasmids
  • Molecular Sequence Data
  • Models, Genetic
  • Gene Expression
  • Enzyme Inhibitors
 

Citation

APA
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MLA
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Del Poeta, M., Toffaletti, D. L., Rude, T. H., Dykstra, C. C., Heitman, J., & Perfect, J. R. (1999). Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target. Genetics, 152(1), 167–178. https://doi.org/10.1093/genetics/152.1.167
Del Poeta, M., D. L. Toffaletti, T. H. Rude, C. C. Dykstra, J. Heitman, and J. R. Perfect. “Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target.Genetics 152, no. 1 (May 1999): 167–78. https://doi.org/10.1093/genetics/152.1.167.
Del Poeta M, Toffaletti DL, Rude TH, Dykstra CC, Heitman J, Perfect JR. Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target. Genetics. 1999 May;152(1):167–78.
Del Poeta, M., et al. “Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target.Genetics, vol. 152, no. 1, May 1999, pp. 167–78. Pubmed, doi:10.1093/genetics/152.1.167.
Del Poeta M, Toffaletti DL, Rude TH, Dykstra CC, Heitman J, Perfect JR. Topoisomerase I is essential in Cryptococcus neoformans: role In pathobiology and as an antifungal target. Genetics. 1999 May;152(1):167–178.

Published In

Genetics

DOI

ISSN

0016-6731

Publication Date

May 1999

Volume

152

Issue

1

Start / End Page

167 / 178

Location

United States

Related Subject Headings

  • Time Factors
  • Sequence Homology, Amino Acid
  • Reverse Transcriptase Polymerase Chain Reaction
  • Radiation, Ionizing
  • Rabbits
  • Plasmids
  • Molecular Sequence Data
  • Models, Genetic
  • Gene Expression
  • Enzyme Inhibitors