Oberstein Adam, Pare Adam, Kaplan Leah, Small Stephen
Department of Biology, New York University, 100 Washington Square East, New York, New York 10003, USA.
Nat Methods. 2005 Aug;2(8):583-5. doi: 10.1038/nmeth775.
Transposons such as P elements are routinely used to stably transfer exogenous DNA (transgenes) into the Drosophila genome. Transgene insertion events, however, are essentially random and are subject to 'position effects' from nearby endogenous regulatory elements. Here we describe a microinjection-based system that uses Cre-mediated recombination to insert transgenes into precise genomic 'landing sites'. The system is simple and efficient, and will permit precise comparisons between multiple transgenic constructs.
诸如P因子这样的转座子通常被用于将外源DNA(转基因)稳定地导入果蝇基因组。然而,转基因插入事件本质上是随机的,并且会受到附近内源调控元件的“位置效应”影响。在此,我们描述了一种基于显微注射的系统,该系统利用Cre介导的重组将转基因插入精确的基因组“着陆位点”。该系统简单高效,将允许对多个转基因构建体进行精确比较。