Spergel D J, Krüth U, Shimshek D R, Sprengel R, Seeburg P H
Department of Molecular Neuroscience, Max-Planck-Institute for Medical Research, Jahnstrasse 29, 69120, Heidelberg, Germany.
Prog Neurobiol. 2001 Apr;63(6):673-86. doi: 10.1016/s0301-0082(00)00038-1.
This review summarizes recent work on the use of reporter genes to label selected neuronal populations in transgenic mice, with particular emphasis on gonadotropin-releasing hormone (GnRH) neurons. Reporter genes discussed are the lacZ, green fluorescent protein (GFP), luc, and bla genes, which encode the reporter proteins beta-galactosidase, GFP, luciferase, and beta-lactamase, respectively. Targeted transgenic expression of these reporter proteins is obtained by fusing the corresponding reporter gene, with or without a subcellular localization signal, to a cell type- or brain region-specific gene promoter. Mice carrying GnRH promoter-driven reporter genes have proven useful for revealing the promoter elements required for cell type-specific expression of GnRH, the full anatomical profile of the GnRH neuronal network, and its electrophysiological activity, suggesting that similar approaches will assist in elucidating the properties of other neuronal populations as well.
本综述总结了近期利用报告基因在转基因小鼠中标记特定神经元群体的研究工作,尤其着重于促性腺激素释放激素(GnRH)神经元。所讨论的报告基因包括lacZ、绿色荧光蛋白(GFP)、luc和bla基因,它们分别编码报告蛋白β-半乳糖苷酶、GFP、荧光素酶和β-内酰胺酶。通过将相应的报告基因(有或没有亚细胞定位信号)与细胞类型或脑区特异性基因启动子融合,可实现这些报告蛋白的靶向转基因表达。携带GnRH启动子驱动的报告基因的小鼠已被证明有助于揭示GnRH细胞类型特异性表达所需的启动子元件、GnRH神经网络的完整解剖结构及其电生理活性,这表明类似方法也将有助于阐明其他神经元群体的特性。