Hashimoto Yukiko, Muramatsu Kazuhiro, Uemura Takefumi, Harada Reiko, Sato Takashi, Okamoto Koichi, Harada Akihiro
Department of Molecular and Cellular Biology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Neuroreport. 2008 Apr 16;19(6):621-4. doi: 10.1097/WNR.0b013e3282fb7d99.
To investigate the neuronal function of genes in vivo, a neuron-specific and inducible gene targeting system is desirable. In this study, we generated a knockin mouse line that expresses a fusion protein consisting of the Cre recombinase and the progesterone receptor (CrePR) in neurons. The neuron-specific expression of CrePR was attained by inserting CrePR gene into the tau locus, because tau is expressed strongly in neurons but scarcely in glias and other tissues. By crossing this knockin mouse line (tau(CrePR)) with ROSA26 lacZ reporter mouse line (R26R), we observed that the antiprogesterone RU486 could induce recombinase activity of the CrePR specifically in neurons. Thus, tau (CrePR) knockin line is a useful tool for studying neuronal gene functions.
为了在体内研究基因的神经元功能,需要一种神经元特异性且可诱导的基因靶向系统。在本研究中,我们构建了一种敲入小鼠品系,该品系在神经元中表达由Cre重组酶和孕酮受体(CrePR)组成的融合蛋白。通过将CrePR基因插入tau基因座来实现CrePR在神经元中的特异性表达,因为tau在神经元中高表达,而在胶质细胞和其他组织中几乎不表达。通过将这种敲入小鼠品系(tau(CrePR))与ROSA26 lacZ报告基因小鼠品系(R26R)杂交,我们观察到抗孕酮RU486可以特异性地在神经元中诱导CrePR的重组酶活性。因此,tau(CrePR)敲入品系是研究神经元基因功能的有用工具。