1. Targeting genes for self-excision in the germ line
- Author
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Joy M. Greer, Kenneth E. Bernstein, Mario R. Capecchi, Michaeline Bunting, and Kirk R. Thomas
- Subjects
Male ,DNA, Complementary ,Somatic cell ,Molecular Sequence Data ,Peptidyl-Dipeptidase A ,Biology ,Germline ,Mice ,Viral Proteins ,Research Communication ,Testis ,Genetics ,Animals ,Site-specific recombinase technology ,Promoter Regions, Genetic ,Gene ,Selectable marker ,Homeodomain Proteins ,Base Sequence ,Integrases ,Gene targeting ,Spermatozoa ,Molecular biology ,Mice, Inbred C57BL ,Gene Targeting ,Female ,Cre-Lox recombination ,Expression cassette ,DNA Damage ,Developmental Biology - Abstract
A procedure is described that directs the self-induced deletion of DNA sequences as they pass through the male germ line of mice. The testes-specific promoter from the angiotensin-converting enzyme gene was used to drive expression of the Cre-recombinase gene. Cre was linked to the selectable marker Neor, and the two genes flanked with loxP elements. This cassette was targeted to the Hoxa3 gene in mouse ES cells that were in turn used to generate chimeric mice. In these chimeras, somatic cells derived from the ES cells retained the cassette, but self-excision occurred in all ES-cell-derived sperm.
- Published
- 1999
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