Related Experiment Video
Updated: Aug 23, 2026

Recombineering Homologous Recombination Constructs in Drosophila
Published on: July 13, 2013
An efficient method to generate chromosomal rearrangements by targeted DNA double-strand breaks in Drosophila
Dieter Egli1, Ernst Hafen, Walter Schaffner
1Institut für Molekularbiologie, CH-8057 Zürich, Switzerland.
Abstract:
Homologous recombination (HR) is an indispensable tool to modify the genome of yeast and mammals. More recently HR is also being used for gene targeting in Drosophila. Here we show that HR can be used efficiently to engineer chromosomal rearrangements such as pericentric and paracentric inversions and translocations in Drosophila. Two chromosomal double-strand breaks (DSBs), introduced by the rare-cutting I-SceI endonuclease on two different mobile elements sharing homologous sequences, are sufficient to promote rearrangements at a frequency of 1% to 4%. Such rearrangements, once generated by HR, can be reverted by Cre recombinase. However, Cre-mediated recombination efficiency drops with increasing distance between recombination sites, unlike HR. We therefore speculate that physical constraints on chromosomal movement are modulated during DSB repair, to facilitate the homology search throughout the genome.
Related Concept Videos
Fixing Double-strand Breaks
Homologous Recombination
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...

