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首页> 外文期刊>Stem cell research >Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology
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Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology

机译:使用CRISPR / CAS9技术生成Rybp纯合敲除鼠ES细胞系Gibhe001-A-1

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RYBP (Ring1 and YY1 Binding Protein) is critical for pluripotency and differentiation of embryonic stem cells (ESCs). RYBP depletion disturbs both neural and myocardial differentiation of ESCs. Moreover, low level of RYBP is correlated with diseases such as glioblastoma. To study the biological function of RYBP in neural differentiation of ESCs, here we generated Rybp homozygous knockout murine ESC line based on Sox1-GFP reporter using CRISPR/Cas9 genome editing technology. The last two exons of Rybp gene in which contain 115 amino acids have been replaced with PGK-Pruo by homologous recombination.
机译:RyBP(Ring1和YY1结合蛋白)对于胚胎干细胞的多能性和分化至关重要(ESC)至关重要。 Rybp Fepletion扰乱了ESC的神经和心肌区别。此外,低水平的RYBP与诸如胶质母细胞瘤的疾病相关。为了研究RYBP在ESC的神经分化中的生物学功能,在这里,我们使用CRISPR / CAS9基因组编辑技术产生了基于SOX1-GFP报告者的Rybp纯合敲除鼠主线。含有115个氨基酸的RyBP基因的最后两个外显子已通过同源重组用PGK-PRUO代替。

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