Fritz A, Rozowski M, Walker C, Westerfield M
Institute of Neuroscience, University of Oregon, Eugene 97403, USA.
Genetics. 1996 Dec;144(4):1735-45. doi: 10.1093/genetics/144.4.1735.
The ease with which mutations can be generated in zebrafish makes this vertebrate an important resource for developmental genetics and genome studies. We have developed a PCR-based screening method that allows the efficient identification of gamma-ray induced deficiencies targeted to selected sequences. We describe three mutants characteristic of our findings and show that these mutations include deletions and translocations that can affect as much as 1% of the genome. These deficiencies provide a basis for analyzing the functions of cloned zebrafish genes using noncomplementation screens for point mutations induced by high-efficiency chemical mutagenesis.
在斑马鱼中能够轻易产生突变,这使得这种脊椎动物成为发育遗传学和基因组研究的重要资源。我们开发了一种基于聚合酶链式反应(PCR)的筛选方法,该方法能够高效鉴定针对特定序列的γ射线诱导的缺失。我们描述了三个体现我们研究结果特征的突变体,并表明这些突变包括缺失和易位,它们可能影响多达1%的基因组。这些缺失为利用针对高效化学诱变诱导的点突变的非互补筛选来分析克隆的斑马鱼基因的功能提供了基础。