Ioffe E, Liu Y, Bhaumik M, Poirier F, Factor S M, Stanley P
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7357-61. doi: 10.1073/pnas.92.16.7357.
Mutant mice produced by gene targeting in embryonic stem (ES) cells often have a complex or embryonic lethal phenotype. In these cases, it would be helpful to identify tissues and cell types first affected in mutant embryos by following the contribution to chimeras of ES cells homozygous for the mutant allele. Although a number of strategies for following ES cell development in vivo have been reported, each has limitations that preclude its general application. In this paper, we describe ES cell lines that can be tracked to every nucleated cell type in chimeras at all developmental stages. These lines were derived from blastocysts of mice that carry an 11-Mb beta-globin transgene on chromosome 3. The transgene is readily detected by DNA in situ hybridization, providing an inert, nuclear-localized marker whose presence is not affected by transcriptional or translational controls. The "WW" series of ES lines possess the essential features of previously described ES lines, including giving rise to a preponderance of male chimeras, all of which have to date exhibited germ-line transmission. In addition, clones selected for single or double targeting events form strong chimeras, demonstrating the feasibility of using WW6 cells to identify phenotypes associated with the creation of a null mutant.
通过对胚胎干细胞(ES细胞)进行基因打靶产生的突变小鼠通常具有复杂或胚胎致死的表型。在这些情况下,通过追踪携带突变等位基因纯合的ES细胞对嵌合体的贡献来确定突变胚胎中首先受影响的组织和细胞类型将是有帮助的。尽管已经报道了许多在体内追踪ES细胞发育的策略,但每种策略都有局限性,妨碍了其广泛应用。在本文中,我们描述了在所有发育阶段都能在嵌合体中追踪到每种有核细胞类型的ES细胞系。这些细胞系源自3号染色体上携带11兆碱基β-珠蛋白转基因的小鼠囊胚。通过DNA原位杂交很容易检测到转基因,提供了一种惰性的、定位于细胞核的标记,其存在不受转录或翻译控制的影响。“WW”系列ES细胞系具有先前描述的ES细胞系的基本特征,包括产生大量雄性嵌合体,迄今为止所有这些嵌合体都表现出种系传递。此外,为单靶向或双靶向事件选择的克隆形成强嵌合体,证明了使用WW6细胞鉴定与产生无效突变相关的表型的可行性。