Institute of Cancer and Genomics Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
MRC London Institute of Medical Sciences and Faculty of Medicine, Imperial College, London, UK.
Methods Mol Biol. 2021;2218:185-194. doi: 10.1007/978-1-0716-0970-5_15.
Here, we describe a fast and straightforward methodology to in vivo detect transcriptional activity in the early zebrafish germ line. We report how fluorescently labeled morpholinos, targeted to nascent early transcripts, can be used to track the onset of transcriptional events during early embryogenesis. This method could be applied to any tagged cell line in a developing early zebrafish embryo as long as the gene of interest is expressed at high enough level for morpholino detection and is expressed at the first and main wave of genome activation, for which the protocol has been verified. The protocol, in combination with genetic manipulation, allows studies of mechanisms driving zygotic genome activation (ZGA) in individual cells. The reported procedures apply to a broad range of purposes for zebrafish embryo manipulation in view of imaging nuclear molecules in specific cell types.
在这里,我们描述了一种快速而直接的方法,可在活体斑马鱼生殖系中检测转录活性。我们报告了如何使用荧光标记的针对新生早期转录本的形态发生素来跟踪早期胚胎发生过程中转录事件的开始。只要感兴趣的基因在用于形态发生素检测的足够高的水平表达,并且在第一个和主要的基因组激活波中表达,该方法就可以应用于发育中的早期斑马鱼胚胎中的任何标记细胞系,该方案已得到验证。该方案与遗传操作相结合,允许在单个细胞中研究驱动合子基因组激活(ZGA)的机制。鉴于在特定细胞类型中成像核分子,所报道的程序适用于广泛的斑马鱼胚胎操作目的。