Research Article
Screening Genes Promoting Exit from Naive Pluripotency Based on Genome-Scale CRISPR-Cas9 Knockout
Figure 1
The screening procedure: (a) outline of the research procedure and (b) technical route. 7 lentiCas9-Blast-expressing mESCs were transfected with GeCKO (v2) lentiGuide-Puro in 2i/LIF, and then input 1 was collected after 48 hours puromycin selection and input 2 after additional 3 passages (9 days) cultured in N2B27+2i/LIF; experimental group was collected after 2 passages of mutation period and 2 passages of 2i/LIF withdrawal and one more passage in 2i/LIF conditions. 2.4E7 stands for 7 mES cells. (c) OG2 mESCs were transfected with Cas9-Blast plasmid and GeCKO v2.0 DNA plasmids in N2B27+2i/LIF medium. Differentiation was enabled by inhibitor removal and enrichment performed by restoring 2i/LIF. (d) Phase and fluorescence images of mES cells at the three stages. Scale bar, 100 μm.
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