GVG Genetic Monitoring GmbH, Deutscher Platz 5b, 04103, Leipzig, Germany.
Genolytic GmbH, Deutscher Platz 5b, 04103, Leipzig, Germany.
Transgenic Res. 2018 Jun;27(3):265-275. doi: 10.1007/s11248-018-0073-2. Epub 2018 Apr 16.
Unclear or misclassified genetic background of laboratory rodents or a lack of strain awareness causes a number of difficulties in performing or reproducing scientific experiments. Until now, genetic differentiation between strains and substrains of inbred mice has been a challenge. We have developed a screening method for analyzing inbred strains regarding their genetic background. It is based on 240 highly informative short tandem repeat (STR) markers covering the 19 autosomes as well as X and Y chromosomes. Combination of analysis results for presence of known C57BL/6 substrain-specific mutations together with autosomal STR markers and the Y-chromosomal STR-haplotype provides a comprehensive snapshot of the genetic background of mice. In this study, the genetic background of 72 mouse lines obtained from 18 scientific institutions in Germany and Austria was determined. By analyzing only 3 individuals per genetically modified line it was possible to detect mixed genetic backgrounds frequently. In several lines presence of a mispairing Y chromosome was detected. At least every second genetically modified line displayed a mixed genetic background which could lead to unexpected and non-reproducible results, irrespective of the investigated gene of interest.
实验室啮齿动物遗传背景不明确或分类错误,或缺乏对品系的认识,这给开展或重现科学实验带来了诸多困难。到目前为止,近交系小鼠的品系和亚系之间的遗传分化一直是一个挑战。我们开发了一种筛选方法,用于分析近交系的遗传背景。该方法基于 240 个高度信息性的短串联重复(STR)标记,覆盖 19 条常染色体以及 X 和 Y 染色体。将存在已知 C57BL/6 亚系特异性突变的分析结果与常染色体 STR 标记和 Y 染色体 STR 单倍型相结合,可全面了解小鼠的遗传背景。在这项研究中,确定了来自德国和奥地利 18 个科研机构的 72 条小鼠品系的遗传背景。通过对每个基因修饰系仅分析 3 个个体,就可以经常检测到混合的遗传背景。在几条线中检测到 Y 染色体错配。至少每第二条基因修饰线显示出混合的遗传背景,这可能导致意外和不可重现的结果,而与所研究的感兴趣的基因无关。