Department of Pathology, Institute of Neuropathology, University Hospital of Zurich, Schmelzbergstrasse, Switzerland.
PLoS One. 2012;7(5):e37881. doi: 10.1371/journal.pone.0037881. Epub 2012 May 29.
Microinjection of DNA constructs into fertilized mouse oocytes typically results in random transgene integration at a single genomic locus. The resulting transgenic founders can be used to establish hemizygous transgenic mouse lines. However, practical and experimental reasons often require that such lines be bred to homozygosity. Transgene zygosity can be determined by progeny testing assays which are expensive and time-consuming, by quantitative Southern blotting which is labor-intensive, or by quantitative PCR (qPCR) which requires transgene-specific design. Here, we describe a zygosity assessment procedure based on fluorescent in situ hybridization (zyFISH). The zyFISH protocol entails the detection of transgenic loci by FISH and the concomitant assignment of homozygosity using a concise and unbiased scoring system. The method requires small volumes of blood, is scalable to at least 40 determinations per assay, and produces results entirely consistent with the progeny testing assay. This combination of reliability, simplicity and cost-effectiveness makes zyFISH a method of choice for transgenic mouse zygosity determinations.
将 DNA 构建体微注射到受精卵的卵母细胞中通常会导致转基因随机整合到单个基因组位置。由此产生的转基因创始者可用于建立半合子转基因小鼠系。然而,实际和实验原因通常要求将这些系繁殖到纯合状态。转基因的杂合性可以通过后代测试分析来确定,该方法昂贵且耗时,通过定量 Southern 印迹法(Southern blot)来确定,该方法劳动强度大,或者通过定量聚合酶链反应(qPCR)来确定,该方法需要转基因特异性设计。在这里,我们描述了一种基于荧光原位杂交(FISH)的杂合性评估程序。zyFISH 方案需要通过 FISH 检测转基因座,并使用简洁且无偏的评分系统同时分配纯合性。该方法需要少量血液,可扩展到每个测定至少 40 个测定,并且结果与后代测试分析完全一致。这种可靠性、简单性和成本效益的结合使 zyFISH 成为转基因小鼠杂合性测定的首选方法。