5.9
CiteScore
5.9
Impact Factor
Volume 35 Issue 7
Jul.  2008
Turn off MathJax
Article Contents

A stringent dual control system overseeing transcription and activity of the Cre recombinase for the liver-specific conditional gene knock-out mouse model

doi: 10.1016/S1673-8527(08)60060-0
More Information
  • Corresponding author: E-mail address: zhujingde@shsci.org (Jingde Zhu)
  • Received Date: 2008-03-21
  • Accepted Date: 2008-05-10
  • Rev Recd Date: 2008-05-09
  • Available Online: 2008-07-18
  • Publish Date: 2008-07-20
  • Liver cancer is one of the most threatening diseases in Chinese population. Just like in other tissues, tumor initiation and development in liver involve multiple steps of genetic and epigenetic alterations with several unknown details. However, unlike in other tissues, a tissue specific inducible Cre recombinase system that allows temporal and spatial deletion of a target DNA fragment is still not available for in vivo functional gene annotation in hepatocytes. In our pursuit to establish such a mouse model, we designed a dual inducible Cre transgene system and tested it in cultured cells. By combining a CCAAT/enhancer binding protein β (C/EBP β) promoter derived Tet-off expression system and the estrogen receptor (ER) mediated functional control, we show a desirable profile of both hepatocyte-specificity and regulability of the Cre expression in a series of critical assessments in the cell culture system, which provides confidence in continuation of our ongoing pursuit in mouse.
  • loading
  • [1]
    Baumgartel, K., Fernandez, C., Johansson, T. et al. Conditional transgenesis and recombination to study the molecular mechanisms of brain plasticity and memory Handb. Exp. Pharmacol., 178 (2007),pp. 315-345
    [2]
    Branda, C.S., Dymecki, S.M. Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice Dev. Cell, 6 (2004),pp. 7-28
    [3]
    Britsch, S. The neuregulin-I/ErbB signaling system in development and disease Adv. Anat. Embryol. Cell Biol., 190 (2007),pp. 1-65
    [4]
    Cai, L., Zhu, J.D. Cell Res., 13 (2003),pp. 93-109
    [5]
    Chung, J.H., Whiteley, M., Felsenfeld, G. Cell, 74 (1993),pp. 505-514
    [6]
    Dale, E.C., Ow, D.W. Intra- and intermolecular site-specific recombination in plant cells mediated by bacteriophage P1 recombinase Gene, 91 (1990),pp. 79-85
    [7]
    Descombes, P., Chojkier, M., Lichtsteiner, S. et al. Genes Dev., 4 (1990),pp. 1541-1551
    [8]
    El-Serag, H.B., Rudolph, K.L. Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis Gastroenterology, 132 (2007),pp. 2557-2576
    [9]
    Erdmann, G., Schutz, G., Berger, S. Inducible gene inactivation in neurons of the adult mouse forebrain BMC Neurosci., 8 (2007),p. 63
    [10]
    Feil, R., Brocard, J., Mascrez, B. et al. Ligand-activated site-specific recombination in mice Proc. Natl. Acad. Sci. USA., 93 (1996),pp. 10887-10890
    [11]
    Feil, R., Wagner, J., Metzger, D. et al. Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains Biochem. Biophys. Res. Commun., 237 (1997),pp. 752-757
    [12]
    Feinberg, A.P. Phenotypic plasticity and the epigenetics of human disease Nature, 447 (2007),pp. 433-440
    [13]
    Frese, K.K., Tuveson, D.A. Maximizing mouse cancer models Nat. Rev. Cancer, 7 (2007),pp. 645-658
    [14]
    Garcia-Otin, A.L., Guillou, F. Mammalian genome targeting using site-specific recombinases Front. Biosci., 11 (2006),pp. 1108-1136
    [15]
    Glaser, S., Anastassiadis, K., Stewart, A.F. Current issues in mouse genome engineering Nat. Genet., 37 (2005),pp. 1187-1193
    [16]
    Gossen, M., Bujard, H. Tight control of gene expression in mammalian cells by tetracycline-responsive promoters Proc. Natl. Acad. Sci. USA., 89 (1992),pp. 5547-5551
    [17]
    Hirrlinger, P.G., Scheller, A., Braun, C. et al. Temporal control of gene recombination in astrocytes by transgenic expression of the tamoxifen-inducible DNA recombinase variant CreERT2 Glia, 54 (2006),pp. 11-20
    [18]
    Kang, K.W., Cho, I.J., Lee, C.H. et al. Essential role of phosphatidylinositol 3-kinase-dependent CCAAT/enhancer binding protein beta activation in the induction of glutathione S-transferase by oltipraz J. Natl. Cancer Inst., 95 (2003),pp. 53-66
    [19]
    Kuhbandner, S., Brummer, S., Metzger, D. et al. Temporally controlled somatic mutagenesis in smooth muscle Genesis, 28 (2000),pp. 15-22
    [20]
    Laurent-Puig, P., Zucman-Rossi, J. Genetics of hepatocellular tumors Oncogene, 25 (2006),pp. 3778-3786
    [21]
    Lavon, I., Goldberg, I., Amit, S. et al. High susceptibility to bacterial infection, but no liver dysfunction, in mice compromised for hepatocyte NF-kappaB activation Nat. Med., 6 (2000),pp. 573-577
    [22]
    Lewandoski, M. Conditional control of gene expression in the mouse Nat. Rev. Genet., 2 (2001),pp. 743-755
    [23]
    Lewandoski, M. Analysis of mouse development with conditional mutagenesis Handb. Exp. Pharmacol, 178 (2007),pp. 235-262
    [24]
    Luedde, T., Duderstadt, M., Streetz, K.L. et al. C/EBP beta isoforms LIP and LAP modulate progression of the cell cycle in the regenerating mouse liver Hepatology, 40 (2004),pp. 356-365
    [25]
    Pikarsky, E., Porat, R.M., Stein, I. et al. NF-kappaB functions as a tumour promoter in inflammation-associated cancer Nature, 431 (2004),pp. 461-466
    [26]
    Rajewsky, K., Gu, H., Kuhn, R. et al. Conditional gene targeting J. Clin. Invest., 98 (1996),pp. 600-603
    [27]
    Schmidt-Supprian, M., Rajewsky, K. Vagaries of conditional gene targeting Nat. Immunol., 8 (2007),pp. 665-668
    [28]
    Schonig, K., Schwenk, F., Rajewsky, K. et al. Nucleic Acids Res., 30 (2002),p. e134
    [29]
    Shelton, P.A., Dart, C. FEBS Lett., 391 (1996),pp. 282-286
    [30]
    Talbot, D., Descombes, P., Schibler, U. Nucleic Acids Res., 22 (1994),pp. 756-766
    [31]
    Utomo, A.R., Nikitin, A.Y., Lee, W.H. Temporal, spatial, and cell type-specific control of Cre-mediated DNA recombination in transgenic mice Nat. Biotechnol., 17 (1999),pp. 1091-1096
    [32]
    Weber, P., Schuler, M., Gerard, C. et al. Temporally controlled site-specific mutagenesis in the germ cell lineage of the mouse testis Biol. Reprod., 68 (2003),pp. 553-559
    [33]
    Xu, J., De Zhu, J., Ni, M. et al. Cell Res., 12 (2002),pp. 177-197
    [34]
    Zhu, J. The altered DNA methylation pattern and its implications in liver cancer Cell Res., 15 (2005),pp. 272-280
    [35]
    Zhu, J., Yao, X. Use of DNA methylation for cancer detection and molecular classification J. Biochem. Mol. Biol., 40 (2007),pp. 135-141
    [36]
    Zhu, J.D., Fei, Q., Wang, P. et al. Cell Res., 16 (2006),pp. 780-796
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (81) PDF downloads (0) Cited by ()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return