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Updated: Sep 27, 2026

Embryo Microinjection for Transgenesis in Drosophila
Published on: June 7, 2024
Transposition of the Drosophila hydei Minos transposon in the mouse germ line
Dubravka Drabek1, Laskaro Zagoraiou, Ton deWit
1Department of Cell Biology and Genetics, Faculty of Medicine, Erasmus University Rotterdam, The Netherlands.
Abstract:
We tested the suitability of the fly transposon Minos, a member of the Tc1/mariner superfamily, for insertional mutagenesis in the mouse germ line. We generated a transgenic mouse line expressing Minos transposase in growing oocytes and another carrying a tandem array of nonautonomous transposons. The frequency of transposition in the progeny derived from oocytes carrying both transgenes is 8.2%. Analysis of the new integration sites shows a high frequency of transpositions to a different chromosome. Thus Minos transposition could be an effective system for insertional mutagenesis and functional genomic analysis in the mouse.
Insights
The Minos transposon system shows promise for insertional mutagenesis in mice. This study demonstrates its effectiveness in the mouse germ line for genetic analysis.
Area of Science:
- Genetics
- Molecular Biology
- Transposon Technology
Background:
- Insertional mutagenesis is a powerful tool for functional genomics.
- Tc1/mariner transposons are mobile genetic elements with potential applications in various organisms.
- The Minos transposon, from the Tc1/mariner superfamily, has been explored for its transposition capabilities.
Purpose of the Study:
- To evaluate the suitability of the Minos transposon system for insertional mutagenesis in the mouse germ line.
- To assess the efficiency and integration patterns of Minos transposition in mice.
- To determine the potential of Minos for functional genomic analysis in mammals.
Main Methods:
- Generation of transgenic mouse lines expressing Minos transposase in oocytes.
- Development of a mouse line carrying nonautonomous Minos transposons.
- Analysis of transposition frequency and integration sites in the progeny.
Main Results:
- A transposition frequency of 8.2% was observed in the progeny from mice carrying both transgenes.
- Analysis of new integration sites revealed a high frequency of transpositions to different chromosomes.
- The Minos system demonstrated successful transposition in the mouse germ line.
Conclusions:
- The Minos transposon system is suitable for insertional mutagenesis in the mouse germ line.
- Minos transposition offers an effective strategy for generating genetic variation in mice.
- This system holds potential for advancing functional genomic studies in the mouse model.

