Leone Dino P, Genoud Stéphane, Atanasoski Suzana, Grausenburger Reinhard, Berger Philipp, Metzger Daniel, Macklin Wendy B, Chambon Pierre, Suter Ueli
Institute of Cell Biology, Department of Biology, Swiss Federal Institute of Technology, ETH Hönggerberg, Zürich, Switzerland.
Mol Cell Neurosci. 2003 Apr;22(4):430-40. doi: 10.1016/s1044-7431(03)00029-0.
Inducible transgenesis provides a valuable technique for the analysis of gene function in vivo. We report the generation and characterization of mouse lines carrying glia lineage-specific transgenes expressing an improved variant of the tamoxifen-inducible Cre recombinase, CreERT2, where the recombinase is fused to a mutated ligand binding domain of the human estrogen receptor. Using a PLP-CreERT2 transgene, we have generated mice that show specific inducible Cre function, as analyzed by cross-breeding experiments into the Rosa26 Cre-LacZ reporter line, in developing and adult Schwann cells, in mature myelinating oligodendrocytes, and in undifferentiated NG2-positive oligodendrocyte precursors in the adult. Using a P0Cx-CreERT2 transgene, we have also established mouse lines with inducible Cre function specifically in the Schwann cell lineage. These tamoxifen-inducible CreERT2 lines will allow detailed spatiotemporally controlled analysis of gene functions in loxP-based conditional mutant mice in both developing and adult Schwann cells and in the oligodendrocyte lineage.
可诱导转基因技术为体内基因功能分析提供了一种有价值的方法。我们报告了携带胶质细胞谱系特异性转基因的小鼠品系的产生和特性,这些转基因表达了一种改进的他莫昔芬诱导型Cre重组酶CreERT2,其中重组酶与人雌激素受体的突变配体结合域融合。利用PLP-CreERT2转基因,我们培育出了小鼠,通过与Rosa26 Cre-LacZ报告基因系杂交实验分析发现,这些小鼠在发育中的和成年的雪旺细胞、成熟的有髓少突胶质细胞以及成年未分化的NG2阳性少突胶质细胞前体细胞中表现出特异性的可诱导Cre功能。利用P0Cx-CreERT2转基因,我们还建立了在雪旺细胞谱系中具有特异性可诱导Cre功能的小鼠品系。这些他莫昔芬诱导型CreERT2品系将允许在发育中和成年的雪旺细胞以及少突胶质细胞谱系中,对基于loxP的条件性突变小鼠的基因功能进行详细的时空控制分析。