Targeting genes for self-excision in the germ line
M Bunting, KE Bernstein, JM Greer… - Genes & …, 1999 - genesdev.cshlp.org
M Bunting, KE Bernstein, JM Greer, MR Capecchi, KR Thomas
Genes & development, 1999•genesdev.cshlp.orgA 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 Neo r, 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 …
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 Neo r, 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 …
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. Crewas linked to the selectable marker Neo r, 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.
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