| Literature DB >> 28409408 |
Jasmin Kristianto1,2, Michael G Johnson3, Ryley K Zastrow3, Abigail B Radcliff3, Robert D Blank4,5,6.
Abstract
Inducible Cre-ERT recombinase technology is widely used for gene targeting studies. The second generation of inducible Cre-ERT recombinase, hemizygous B6.129S-Tg(UBC-cre/ERT2)1Ejb/J (hereafter abbreviated as Cre-ERT2), a fusion of a mutated estrogen receptor and Cre recombinase, was engineered to be more efficient and specific than the original Cre-ERT. The putative mechanism of selective Cre-mediated recombination is Cre sequestration in the cytoplasm in the basal state with translocation to the nucleus only in the presence of tamoxifen. We utilized both a reporter mouse (B6.129 (Cg)-Gt(ROSA)26Sor tm4(ACTB-tdTomato,-EGFP)Luo /J) and endothelin converting enzyme-1 floxed transgenic mouse line to evaluate Cre-ERT2 activity. We observed spontaneous Cre activity in both settings. Unintended Cre activity is a confounding factor that has a potentially large impact on data interpretation. Thus, it is important to consider background Cre activity in experimental design.Entities:
Keywords: Cre-activity; Estrogen receptor; Recombination; Tamoxifen
Mesh:
Substances:
Year: 2017 PMID: 28409408 PMCID: PMC9474299 DOI: 10.1007/s11248-017-0018-1
Source DB: PubMed Journal: Transgenic Res ISSN: 0962-8819 Impact factor: 3.145