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Developmental and adult phenotyping directly from mutant embryonic stem cells

机译:直接从突变的胚胎干细胞发育和成年表型

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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 trans-genic 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.
机译:四倍体胚胎互补测定表明,单独的小鼠ES细胞能够支持小鼠的胚胎发育和成年生活。新近建立的F_1杂种ES细胞允许以足够高的效率生产ES细胞衍生的动物,从而直接使基于ES细胞的遗传学变得可行。在这里,我们报告了12种新的F_1杂交ES细胞系的建立和表征,以及在功能获得和丧失功能的遗传研究中使用了最好的(G4)之一,其中直接从ES细胞评估了体内表型来源的胚胎。我们发现生成G4 ES细胞的动物非常有效。此外,即使经过连续两轮的遗传修饰,大多数转基因品系仍​​保留了亲本品系的原始潜力。与产生ES细胞的动物/胚胎产生嵌合体的比例为10-40%。使用这些经过遗传修饰的ES细胞,在大多数情况下,这种成功率允许在建立细胞系后仅几周的时间内衍生出足够数量的突变体用于初始表型分析。尽管实验设计必须考虑到中等程度的ES细胞系不受控制的损伤,但是我们的原理验证实验提供了有用的数据,以帮助未来的设计利用该技术的力量来加速我们对基因功能的理解。

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