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Updated: Aug 14, 2026

Selection-dependent and Independent Generation of CRISPR/Cas9-mediated Gene Knockouts in Mammalian Cells
Published on: June 16, 2017
Identification of low frequency knockout mutants in Dictyostelium discoideum created by single or double homologous
Steve J Charette1, Sophie Cornillon, Pierre Cosson
1Université de Genève, Centre Médical Universitaire, Département de Physiologie Cellulaire et Métabolisme, Switzerland. charett2@etu.unige.ch
Abstract:
Generation and characterization of knockout clones is a widely used approach to evaluate the specific function of a gene product in Dictyostelium discoideum. The mutant clones are generally obtained by double homologous recombination in the target gene. A frequent limitation to obtaining mutants is the low frequency of homologous recombination. Here we present an easy method to identify rare mutants, based on PCR analysis of pools of clones. This method also allows the isolation of functional knockout mutants created by a single homologous recombination event, which can be more frequent than a double recombination event.

