Spontaneous recombinase activity of Cre-ERT2 in vivo

被引:46
|
作者
Kristianto, Jasmin [1 ,2 ]
Johnson, Michael G. [4 ]
Zastrow, Ryley K. [4 ]
Radcliff, Abigail B. [4 ]
Blank, Robert D. [1 ,2 ,3 ]
机构
[1] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[2] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA
[3] Milwaukee VA Med Ctr, Milwaukee, WI USA
[4] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI USA
关键词
Tamoxifen; Estrogen receptor; Recombination; Cre-activity; TETRACYCLINE-RESPONSIVE PROMOTERS; GENE-EXPRESSION; TIGHT CONTROL; MICE; MUTAGENESIS; VECTORS; CELLS;
D O I
10.1007/s11248-017-0018-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:411 / 417
页数:7
相关论文
共 50 条
  • [31] Primary Spermatocyte-Specific Cre Recombinase Activity in Transgenic Mice
    Sanny S. W. Chung
    François Cuzin
    Minoo Rassoulzadegan
    Debra J. Wolgemuth
    Transgenic Research, 2004, 13 : 289 - 294
  • [32] Primary spermatocyte-specific Cre recombinase activity in transgenic mice
    Chung, SSW
    Cuzin, F
    Rassoulzadegan, M
    Wolgemuth, DJ
    TRANSGENIC RESEARCH, 2004, 13 (03) : 289 - 294
  • [33] A transgenic mouse line that retains Cre recombinase activity in mature oocytes irrespective of the cre transgene transmission
    Sakai, K
    Miyazaki, J
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 237 (02) : 318 - 324
  • [34] Using Cre-recombinase-driven Polylox barcoding for in vivo fate mapping in mice
    Pei, Weike
    Wang, Xi
    Roessler, Jens
    Feyerabend, Thorsten B.
    Hoefer, Thomas
    Rodewald, Hans-Reimer
    NATURE PROTOCOLS, 2019, 14 (06) : 1820 - 1840
  • [35] Using Cre-recombinase-driven Polylox barcoding for in vivo fate mapping in mice
    Weike Pei
    Xi Wang
    Jens Rössler
    Thorsten B. Feyerabend
    Thomas Höfer
    Hans-Reimer Rodewald
    Nature Protocols, 2019, 14 : 1820 - 1840
  • [36] Sites of Cre-recombinase activity in mouse lines targeting skeletal cells
    Couasnay, Greig
    Madel, Maria-Bernadette
    Lim, Joohyun
    Lee, Brendan
    Elefteriou, Florent
    JOURNAL OF BONE AND MINERAL RESEARCH, 2021, 36 (09) : 1661 - 1679
  • [37] Sertoli and granulosa cell-specific Cre recombinase activity in transgenic mice
    Lécureuil, C
    Fontaine, I
    Crepieux, P
    Guillou, F
    GENESIS, 2002, 33 (03) : 114 - 118
  • [38] Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice
    Lan, ZJ
    Xu, XP
    Cooney, AJ
    BIOLOGY OF REPRODUCTION, 2004, 71 (05) : 1469 - 1474
  • [39] Epididymal initial segment-specific Cre recombinase activity in Lcn8-Cre knock-in mice
    Gong, Qian-qian
    Dou, Zhi-lin
    Wang, Xiao
    Zhang, Ke-yi
    Chen, Hao
    Gao, Jian-gang
    Sun, Xiao-yang
    MOLECULAR BIOLOGY REPORTS, 2021, 48 (08) : 6015 - 6023
  • [40] Epididymal initial segment-specific Cre recombinase activity in Lcn8-Cre knock-in mice
    Qian-qian Gong
    Zhi-lin Dou
    Xiao Wang
    Ke-yi Zhang
    Hao Chen
    Jian-gang Gao
    Xiao-yang Sun
    Molecular Biology Reports, 2021, 48 : 6015 - 6023