| First Author | de Wit T | Year | 2010 |
| Journal | Mol Cell Biol | Volume | 30 |
| Issue | 1 | Pages | 68-77 |
| PubMed ID | 19884347 | Mgi Jnum | J:156413 |
| Mgi Id | MGI:4420514 | Doi | 10.1128/MCB.00913-09 |
| Citation | de Wit T, et al. (2010) Tagged mutagenesis by efficient Minos-based germ line transposition. Mol Cell Biol 30(1):68-77 |
| abstractText | Germ line gene transposition technology has been used to generate 'libraries' of flies and worms carrying genomewide mutations. Phenotypic screening and DNA sequencing of such libraries provide functional information resulting from insertional events in target genes. There is also a great need to have a fast and efficient way to generate mouse mutants in vivo to model developmental defects and human diseases. Here we describe an optimized mammalian germ line transposition system active during early mouse spermatogenesis using the Minos transposon. Transposon-positive progeny carry on average more than 2 new transpositions, and 45 to 100% of the progeny carry an insertion in a gene. The optimized Minos-based system was tested in a small rapid dominant functional screen to identify mutated genes likely to cause measurable cardiovascular 'disease' phenotypes in progeny/embryos. Importantly this system allows rapid screening for modifier genes. |
