George Sophia H L, Gertsenstein Marina, Vintersten Kristina, Korets-Smith Ella, Murphy John, Stevens Mary E, Haigh Jody J, Nagy Andras
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario, Canada M5G 1X5.
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4455-60. doi: 10.1073/pnas.0609277104. Epub 2007 Mar 2.
Tetraploid embryo complementation assay has shown that mouse ES cells alone are capable of supporting embryonic development and adult life of mice. Newly established F(1) hybrid ES cells allow the production of ES cell-derived animals at a high enough efficiency to directly make ES cell-based genetics feasible. Here we report the establishment and characterization of 12 new F(1) hybrid ES cell lines and the use of one of the best (G4) in a gain- and loss-of-function genetic study, where the in vivo phenotypes were assessed directly from ES cell-derived embryos. We found the generation of G4 ES cell-derived animals to be very efficient. Furthermore, even after two consecutive rounds of genetic modifications, the majority of transgenic lines retained the original potential of the parental lines; with 10-40% of chimeras producing ES cell-derived animals/embryos. Using these genetically altered ES cells, this success rate, in most cases, permitted the derivation of a sufficient number of mutants for initial phenotypic analyses only a few weeks after the establishment of the cell lines. Although the experimental design has to take into account a moderate level of uncontrolled damage on ES cell lines, our proof-of-principle experiment provides useful data to assist future designs harnessing the power of this technology to accelerate our understanding of gene function.
四倍体胚胎互补试验表明,仅小鼠胚胎干细胞就能支持小鼠的胚胎发育和成年生活。新建立的F(1)杂交胚胎干细胞能以足够高的效率产生胚胎干细胞衍生动物,从而使基于胚胎干细胞的遗传学直接可行。在此,我们报告12种新的F(1)杂交胚胎干细胞系的建立和特性,并在功能获得和功能丧失的遗传学研究中使用其中最好的一种(G4),其中体内表型直接从胚胎干细胞衍生的胚胎中评估。我们发现G4胚胎干细胞衍生动物的产生非常高效。此外,即使经过两轮连续的基因改造,大多数转基因系仍保留了亲代系的原始潜能;10%-40%的嵌合体产生胚胎干细胞衍生动物/胚胎。使用这些基因改造的胚胎干细胞,在大多数情况下,这种成功率使得仅在细胞系建立后几周就能获得足够数量的突变体用于初步表型分析。尽管实验设计必须考虑到对胚胎干细胞系的适度失控损伤,但我们的原理验证实验提供了有用的数据,以协助未来利用该技术的力量来加速我们对基因功能理解的设计。