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Controlled re-activation of epigenetically silenced Tet promoter-driven transgene expression by targeted demethylation

机译:通过靶向去甲基化控制再激活外延沉默的TET启动子驱动的转基因表达

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摘要

Faithful expression of transgenes in cell cultures and mice is often challenged by locus dependent epigenetic silencing. We investigated silencing of Tet-controlled expression cassettes within the mouse ROSA26 locus. We observed pronounced DNA methylation of the Tet promoter concomitant with loss of expression in mES cells as well as in differentiated cells and transgenic animals. Strikingly, the ROSA26 promoter remains active and methylation free indicating that this silencing mechanism specifically affects the transgene, but does not spread to the host's chromosomal neighborhood. To reactivate Tet cassettes a synthetic fusion protein was constructed and expressed in silenced cells. This protein includes the enzymatic domains of ten eleven translocation methylcytosine dioxygenase 1 (TET-1) as well as the Tet repressor DNA binding domain. Expression of the synthetic fusion protein and Doxycycline treatment allowed targeted demethylation of the Tet promoter in the ROSA26 locus and in another genomic site, rescuing transgene expression in cells and transgenicmice. Thus, inducible, reversible and site-specific epigenetic modulation is a promising strategy for reactivation of silenced transgene expression, independent of the integration site.
机译:忠实的细胞培养物和小鼠的转基因表达通常是源于依赖的表观遗传沉默的挑战。我们调查了鼠标ROSA26基因座内的TET控制表达式盒的沉默。我们观察到TET启动子的显着DNA甲基化伴随着MES细胞中的表达损失以及分化细胞和转基因动物。令人惊讶的是,ROSA26启动子保持活性和甲基化,表明该沉默机制特异性影响转基因,但不会蔓延到宿主的染色体邻域。重新激活TET盒子,在沉默的细胞中构建合成融合蛋白并表达。该蛋白质包括十一易位甲基胞嘧啶二恶英酶1(TET-1)的酶域以及TET抑制剂DNA结合结构域。合成融合蛋白和催生素治疗的表达允许罗斯启动子的靶向去甲基化在ROSA26基因座中和另一个基因组位点,抵押细胞和转基因的转基因表达。因此,诱导型,可逆和特异性的表观遗传调节是重新激活沉默的转基因表达的有希望的策略,与整合位点无关。

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  • 来源
    《Nucleic Acids Research》 |2017年第16期|共14页
  • 作者单位

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

    Univ Hosp Dept Internal Med 3 Regensburg Germany;

    Helmholtz Ctr Infect Res Dept Sci Strategy Braunschweig Germany;

    Helmholtz Ctr Infect Res RG Model Syst Infect &

    Immun MSYS Braunschweig Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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