Joining forces: first application of a rapamycin-induced dimerizable Cre system for conditional null mutant analysis in Leishmania

Mol Microbiol. 2016 Jun;100(6):923-7. doi: 10.1111/mmi.13374. Epub 2016 Apr 20.

Abstract

Reverse genetics in Leishmania spp has gained importance beyond basic research as efforts increase to discover and validate new drug targets. Often, the most promising targets are essential for viability of the parasites, defying a genetic analysis by current gene replacement strategies. Duncan et al. demonstrate the applicability of DiCre recombination in Leishmania for induced replacement of the kinase CRK3 gene in promastigotes. DiCre gene replacement leads to the rapid loss of the gene and allows monitoring the phenotypic effects of the loss of function, eliminating the need for prolonged cultivation and selection. Implementation of the DiCre approach will allow functional genetics of the most important of Leishmania genes and is likely to boost genetic research and drug target discovery.

Publication types

  • Comment

MeSH terms

  • Antiprotozoal Agents / pharmacology
  • Integrases / genetics
  • Integrases / metabolism
  • Leishmania / drug effects
  • Leishmania / enzymology
  • Leishmania / genetics*
  • Molecular Targeted Therapy
  • Proto-Oncogene Proteins c-crk / genetics
  • Reverse Genetics / methods*
  • Sirolimus / pharmacology*

Substances

  • Antiprotozoal Agents
  • Proto-Oncogene Proteins c-crk
  • Cre recombinase
  • Integrases
  • Sirolimus