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Single-stranded template DNA and guide RNAs were microinjected into C57BL/6J embryos and implanted into foster mothers to result in gene-edited F0 mice. F0 mice with the desired mutation were mated to animals that harbored the Cre deleter allele (Tg(KRT14-cre/ERT2)1Ipc - MGI:2177426) and the mTmG reporter allele (Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo - MGI:3716464) of uncertain genetic background (“K14-CreER; mTmG” in PMID:11034212 and 17868096) to produce the F1 generation. F1 animals that did not harbor the K14-CreER allele were crossed with B6J(FVB)-congenic beta-actin cre mice (Tmem163Tg(ACTB-cre)2Mrt - MGI:2176050) to test if the floxed allele can recombine successfully. Cre-negative F2 progeny were sib-mated thereafter, and the mTmG allele was bred out.
Li M, Indra AK, Warot X, Brocard J, Messaddeq N, Kato S, Metzger D, Chambon P. Skin abnormalities generated by temporally controlled RXRalpha mutations in mouse epidermis. Nature. 2000 Oct 5;407(6804):633-6. doi: 10.1038/35036595. (Medline PMID: 11034212)
Muzumdar MD, Tasic B, Miyamichi K, Li L, Luo L. A global double-fluorescent Cre reporter mouse. Genesis. 2007 Sep;45(9):593-605. doi: 10.1002/dvg.20335. (Medline PMID: 17868096)
Colony Surveillance Program and Current Health Reports
When this strain becomes available, Limited quantities of breeder mice (recovered litter) are available from a cryoarchive; recovered litter usually available to ship in 3 to 4 months.
Cryopreserved material may be available upon request, please inquire to mmrrc@ucdavis.edu for more information.
The donor or their institution limits the distribution to non-profit institutions only.
Distribution of this strain requires submission of the MMRRC Conditions of Use (COU). A link to the COU web form will be provided via email after an order has been placed; the form should be completed then or the email forwarded to your institutional official for completion.