Wilson C, Pearson R K, Bellen H J, O'Kane C J, Grossniklaus U, Gehring W J
Department of Cell Biology, Biozentrum, University of Basel, Switzerland.
Genes Dev. 1989 Sep;3(9):1301-13. doi: 10.1101/gad.3.9.1301.
We describe a new approach for identifying and studying genes involved in Drosophila development. Single copies of an enhancer detector transposon, P[1ArB], have been introduced into flies at many different genomic locations. The beta-galactosidase reporter gene in this construct is influenced by a wide range of genomic transcriptional regulatory elements in its vicinity. Our results suggest that a significant proportion of these regulatory sequences are control elements of nearby Drosophila genes. These genes need not be disrupted for their regulatory elements to be identified by P[1ArB]. The P[1ArB] transposon has been designed to facilitate both rapid cloning and deletion analysis of genomic sequences into which it inserts. Therefore, the enhancer detection system is an efficient method of screening for genes primarily on the basis of their expression pattern and then rapidly analyzing those of particular interest at the molecular and genetic levels.
我们描述了一种鉴定和研究参与果蝇发育的基因的新方法。增强子检测转座子P[1ArB]的单拷贝已被引入果蝇的许多不同基因组位置。该构建体中的β-半乳糖苷酶报告基因受其附近广泛的基因组转录调控元件的影响。我们的结果表明,这些调控序列中有很大一部分是附近果蝇基因的控制元件。这些基因的调控元件无需被破坏即可通过P[1ArB]进行鉴定。P[1ArB]转座子的设计便于对其插入的基因组序列进行快速克隆和缺失分析。因此,增强子检测系统是一种主要基于基因表达模式筛选基因,然后在分子和遗传水平上快速分析那些特别感兴趣基因的有效方法。