4.2 Article

Spontaneous recombinase activity of Cre-ERT2 in vivo

Journal

TRANSGENIC RESEARCH
Volume 26, Issue 3, Pages 411-417

Publisher

SPRINGER
DOI: 10.1007/s11248-017-0018-1

Keywords

Tamoxifen; Estrogen receptor; Recombination; Cre-activity

Funding

  1. Office of Research and Development, Rehabilitation Research and Development Service
  2. Merit Review Award from Office of Research and Development, Biomedical and Laboratory Research and Development Service, the Department of Veterans Affairs
  3. National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institute of Health [NIH AR54753]
  4. [I21 RX1440]

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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.

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