Oberto Alessandra, Acquadro Elena, Bus Thorsten, Sprengel Rolf, Eva Carola
Dipartimento di Anatomia, Farmacologia e Medicina Legale, Sezione di Farmacologia, Via Pietro Giuria 13, 10125 Torino, Italy.
Eur J Neurosci. 2007 Jul;26(1):155-70. doi: 10.1111/j.1460-9568.2007.05631.x.
In the rat brain, neuropeptide Y (NPY) Y(1) and Y(5) receptors are coexpressed in various forebrain regions where they mediate several NPY-activated functions, including feeding behaviour, anxiety, neuronal excitability and hormone secretion. We studied the distribution pattern and cellular colocalization of the Y(1) and the Y(5) receptor gene expression in the mouse brain by using transgenic mice with genomically integrated BAC clones, where the coding regions of the Y(1) and Y(5) receptor genes were replaced by Venus and the synthetic transcription factor itTA reporter genes, respectively (Tg(Y5RitTA/Y1RVenus) mice). Analysis of Venus fluorescence and itTA-mediated activation of Cre recombinase revealed copy number-dependent expression levels, between the lines, but similar expression patterns. In three transgenic lines the BAC encoded Y(5) receptor promoter induced strong Cre expression in the olfactory system, cerebral cortex, hippocampus and basal ganglia. Weaker expression was found in most of the hypothalamic nuclei of line 25, the highest-expressing transgenic line. Activation of Cre was itTA-dependent and could be regulated by doxycycline. The Y(1) receptor promoter-induced Venus fluorescence was intense, widely present through the brain and colocalized with Cre immunostaining in neurons of distinct brain regions, including the cerebral cortex, basolateral amygdala, dentate gyrus and paraventricular nucleus. These data provide a detailed and comparative mapping of Y(1) and Y(5) receptor promoter activity within cells of the mouse brain. The Tg(Y5RitTA/Y1RVenus)-transgenic mice generated here also represent a genetic tool for conditional mutagenesis via the Cre lox system, particularly of genes involved in feeding behaviour, neuronal excitability and hormone secretion.
在大鼠脑中,神经肽Y(NPY)的Y(1)和Y(5)受体在多个前脑区域共表达,介导多种NPY激活的功能,包括进食行为、焦虑、神经元兴奋性和激素分泌。我们通过使用基因组整合BAC克隆的转基因小鼠,研究了小鼠脑中Y(1)和Y(5)受体基因表达的分布模式和细胞共定位情况,其中Y(1)和Y(5)受体基因的编码区域分别被金星荧光蛋白(Venus)和合成转录因子itTA报告基因取代(Tg(Y5RitTA/Y1RVenus)小鼠)。对金星荧光和itTA介导的Cre重组酶激活的分析显示,不同品系之间存在拷贝数依赖性的表达水平,但表达模式相似。在三个转基因品系中,BAC编码的Y(5)受体启动子在嗅觉系统、大脑皮层、海马体和基底神经节中诱导强烈的Cre表达。在表达最高的转基因品系25的大多数下丘脑核中发现较弱的表达。Cre的激活依赖于itTA,并且可以由强力霉素调节。Y(1)受体启动子诱导的金星荧光强烈,广泛存在于整个大脑中,并与不同脑区(包括大脑皮层、基底外侧杏仁核、齿状回和室旁核)神经元中的Cre免疫染色共定位。这些数据提供了小鼠脑内细胞中Y(1)和Y(5)受体启动子活性的详细比较图谱。此处生成的Tg(Y5RitTA/Y1RVenus)转基因小鼠还代表了一种通过Cre-lox系统进行条件诱变的遗传工具,特别是用于涉及进食行为、神经元兴奋性和激素分泌的基因。