Babu Swathy, Nishiwaki Yuko, Masai Ichiro
Developmental neurobiology unit, Okinawa Institute of Science and Technology Graduate University, Onna, Japan.
Bio Protoc. 2025 Mar 20;15(6):e5248. doi: 10.21769/BioProtoc.5248.
Zebrafish genetic mutants have emerged as a valuable model system for studying various aspects of disease and developmental biology. Mutant zebrafish embryos are generally identified based on phenotypic defects at later developmental stages, making it difficult to investigate underlying molecular mechanisms at earlier stages. This protocol presents a PCR-based genotyping method that enables the identification of wild-type, heterozygous, and homozygous zebrafish genetic mutants at any developmental stage, even when they are phenotypically indistinguishable. The approach involves the amplification of specific genomic regions using carefully designed primers, followed by gel electrophoresis. This genotyping method facilitates the investigation of the molecular mechanisms driving phenotypic defects that are observed at later timepoints. This protocol allows researchers to perform analyses such as immunofluorescence, RT-PCR, RNA sequencing, and other molecular experiments on early developmental stages of mutants. The availability of this protocol expands the utility of zebrafish genetic mutants for elucidating the molecular underpinnings of various biological processes throughout development. Key features • Enables genotyping of zebrafish genetic mutants at any developmental stage, even before the onset of phenotypic defects. • Utilizes PCR amplification and restriction enzyme digestion to distinguish wild-type, mutant, and heterozygous genotypes.
斑马鱼基因变异体已成为研究疾病和发育生物学各个方面的重要模型系统。突变斑马鱼胚胎通常是根据后期发育阶段的表型缺陷来识别的,这使得在早期阶段研究潜在分子机制变得困难。本方案介绍了一种基于聚合酶链反应(PCR)的基因分型方法,该方法能够在任何发育阶段识别野生型、杂合子和纯合子斑马鱼基因变异体,即使它们在表型上难以区分。该方法包括使用精心设计的引物扩增特定基因组区域,然后进行凝胶电泳。这种基因分型方法有助于研究在后期时间点观察到的驱动表型缺陷的分子机制。本方案允许研究人员对变异体的早期发育阶段进行免疫荧光、逆转录聚合酶链反应(RT-PCR)、RNA测序和其他分子实验等分析。该方案的可用性扩展了斑马鱼基因变异体在阐明整个发育过程中各种生物学过程的分子基础方面的效用。关键特性 • 能够在任何发育阶段对斑马鱼基因变异体进行基因分型,甚至在表型缺陷出现之前。 • 利用PCR扩增和限制性内切酶消化来区分野生型、突变型和杂合子基因型。