Hughes Elizabeth D, Qu Yun Yan, Genik Suzanne J, Lyons Robert H, Pacheco Christopher D, Lieberman Andrew P, Samuelson Linda C, Nasonkin Igor O, Camper Sally A, Van Keuren Margaret L, Saunders Thomas L
Transgenic Animal Model Core, Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Mamm Genome. 2007 Aug;18(8):549-58. doi: 10.1007/s00335-007-9054-0. Epub 2007 Sep 9.
Genetically modified mouse strains derived from embryonic stem (ES) cells are powerful tools for gene function analysis. ES cells from the C57BL/6 mouse strain are not widely used to generate mouse models despite the advantage of a defined genetic background. We assessed genetic variation in six such ES cell lines with 275 SSLP markers. Compared to C57BL/6, Bruce4 differed at 34 SSLP markers and had significant heterozygosity on three chromosomes. BL/6#3 and Dale1 ES cell lines differed at only 3 SSLP makers. The C2 and WB6d ES cell lines differed at 6 SSLP markers. It is important to compare the efficiency of producing mouse models with available C57BL/6 ES cells relative to standard 129 mouse strain ES cells. We assessed genetic stability (the tendency of cells to become aneuploid) in 110 gene-targeted ES cell clones from the most widely used C57BL/6 ES cell line, Bruce4, and 710 targeted 129 ES cell clones. Bruce4 clones were more likely to be aneuploid and unsuitable for ES cell-mouse chimera production. Despite their tendency to aneuploidy and consequent inefficiency, use of Bruce4 ES cells can be valuable for models requiring behavioral studies and other mouse models that benefit from a defined C57BL/6 background.
源自胚胎干细胞(ES细胞)的基因工程小鼠品系是进行基因功能分析的有力工具。尽管C57BL/6小鼠品系的ES细胞具有明确遗传背景的优势,但并未广泛用于构建小鼠模型。我们用275个简单序列长度多态性(SSLP)标记评估了6个此类ES细胞系的遗传变异。与C57BL/6相比,Bruce4在34个SSLP标记上存在差异,并且在三条染色体上具有显著的杂合性。BL/6#3和Dale1 ES细胞系仅在3个SSLP标记上存在差异。C2和WB6d ES细胞系在6个SSLP标记上存在差异。相对于标准的129小鼠品系ES细胞,比较使用现有C57BL/6 ES细胞构建小鼠模型的效率很重要。我们评估了来自最常用的C57BL/6 ES细胞系Bruce4的110个基因靶向ES细胞克隆和710个靶向129 ES细胞克隆的遗传稳定性(细胞变成非整倍体的倾向)。Bruce4克隆更有可能是非整倍体,不适合用于ES细胞-小鼠嵌合体的构建。尽管它们有非整倍体的倾向以及随之而来的低效率,但对于需要行为研究的模型和其他受益于明确C57BL/6背景的小鼠模型而言,使用Bruce4 ES细胞可能是有价值的。