Nakamura Shuhei, Saito Daisuke, Tanaka Minoru
Laboratory of Molecular Genetics for Reproduction, National Institute for Basic Biology, Okazaki, Japan.
Dev Growth Differ. 2008 Aug;50(6):415-9. doi: 10.1111/j.1440-169X.2008.01027.x. Epub 2008 Apr 16.
The availability of bacterial artificial chromosome (BAC) offers a good genomic platform for a targeted integration of an exogenous gene by a homologous recombination system in Escherichia coli. In combination with microinjection technology, this system allows for the analysis of various aspects of biological phenomena occurring in vivo using Japanese medaka fish (Oryzias latipes). Here we describe a streamlined procedure for selecting BAC clones based on the medaka University of Tokyo genome browser (UTGB), followed by rapid modification with enhanced green fluorescent protein (EGFP) or DsRed fragments for transgenic analysis in medaka. Experimental procedures for BAC DNA preparation, microinjection of medaka embryos and screening of resulting transgenic medaka carrying EGFP/DsRed modified BAC clones are also described.
细菌人工染色体(BAC)的可用性为通过大肠杆菌中的同源重组系统进行外源基因的靶向整合提供了一个良好的基因组平台。结合显微注射技术,该系统可用于分析日本青鳉鱼(Oryzias latipes)体内发生的各种生物学现象。在此,我们描述了一种基于青鳉东京大学基因组浏览器(UTGB)选择BAC克隆的简化程序,随后用增强型绿色荧光蛋白(EGFP)或DsRed片段进行快速修饰,用于青鳉的转基因分析。还描述了BAC DNA制备、青鳉胚胎显微注射以及筛选携带EGFP/DsRed修饰BAC克隆的转基因青鳉的实验程序。