Abstract
We have established a transgenic mouse line in which floxed neomycin resistant cassette was inserted between the CAG promoter and EGFP. When these transgenic mice were mated with Cre-expressing transgenic animals, the offspring obtained were fluorescent green. We then established a transgenic mouse line in which EGFP in the above construct was replaced by diphtheria toxin A chain (DT). When the latter transgenic mice were mated with mice expressing Cre restricted to germ cells, we obtained healthy but sterile offspring due to a disruption of germ line cells by DT expression. We predict that this strategy will be useful for the construction of new animal models for human diseases, featuring a variety of missing cell lineages produced by disruption with DT.
Original language | English |
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Pages (from-to) | 275-279 |
Number of pages | 5 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 321 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2004 Aug 20 |
Externally published | Yes |
Keywords
- Animal model for human disease
- Cell lineage specific disruption
- Cre
- Diphtheria toxin
- EGFP
- LoxP
- Transgenic mouse
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology