Phelps C B, Brand A H
Wellcome/CRC Institute, Cambridge University, United Kingdom.
Methods. 1998 Apr;14(4):367-79. doi: 10.1006/meth.1998.0592.
Expressing a gene in cells in which it is not normally active is a powerful way of determining its function. The GAL4 system allows the selective expression of any cloned gene in a wide variety of cell- and tissue-specific patterns in Drosophila. A promoter (or enhancer) directs expression of the yeast transcriptional activator GAL4 in a particular pattern, and GAL4 in turn directs transcription of the GAL4-responsive (UAS) target gene in an identical pattern. The system's key feature is that the GAL4 gene and UAS-target gene are initially separated into two distinct transgenic lines. In the GAL4 line, the activator protein is present, but has no target gene to activate. In the UAS-target gene line, the target gene is silent because the activator is absent. It is only when the GAL4 line is crossed to the UAS-target gene line that the target gene is turned on in the progeny. In this article we describe, in detail, how to generate and characterize GAL4 lines and how to prepare UAS-target gene lines. Vector maps are provided for pGaTB, P[GawB], and pP[UAST]. In addition, we consider the range of UAS-reporters currently available and review several new modifications of the GAL4 system.
在通常不活跃的细胞中表达基因是确定其功能的一种有效方法。GAL4系统允许在果蝇的多种细胞和组织特异性模式中选择性表达任何克隆基因。启动子(或增强子)以特定模式指导酵母转录激活因子GAL4的表达,而GAL4反过来以相同模式指导GAL4反应性(UAS)靶基因的转录。该系统的关键特征是GAL4基因和UAS靶基因最初被分成两个不同的转基因品系。在GAL4品系中,激活蛋白存在,但没有靶基因可激活。在UAS靶基因品系中,由于缺乏激活剂,靶基因处于沉默状态。只有当GAL4品系与UAS靶基因品系杂交时,靶基因才会在后代中开启。在本文中,我们详细描述了如何生成和鉴定GAL4品系以及如何制备UAS靶基因品系。提供了pGaTB、P[GawB]和pP[UAST]的载体图谱。此外,我们考虑了目前可用的UAS报告基因的范围,并回顾了GAL4系统的几种新改进。