Simultaneous transient expression assays of the trypanosomatid parasite Leishmania using β-galactosidase and β-glucuronidase as reporter enzymes

Jonathan H. LeBowitz, Cara M. Coburn, Stephen M. Beverley

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

We describe a transient transfection protocol for cultured Leishmania major promastigotes, utilizing Escherichia coli genes encoding β-galactosidase and β-glucuronidase inserted into an expression vector derived from the dihydrofolate reductase-thymidylate synthase locus. Less than 0.1 pg of either reporter enzyme can be detected with a simple fluorimetric assay, and transfection of 10 μg of either reporter construct yields activities at least 100-fold over background. Simultaneous introduction of both constructs showed that the activity of each reporter gene was unaffected by the presence of the other, allowing one reporter construct to serve as a control for experimental variability in test gene constructs containing the second reporter gene. These results show that it is feasible to apply transient expression assays to the identification of cis-acting elements of genes encoding nonabundant mRNAs in the genus Leishmania.

Original languageEnglish
Pages (from-to)119-123
Number of pages5
JournalGene
Volume103
Issue number1
DOIs
StatePublished - Jul 15 1991

Keywords

  • DNA transfection
  • Kinetoplastida
  • Recombinant DNA
  • protozoan parasite

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