To overcome the low CRISPR-Cas9 editing efficiency at the TERT locus, the scientists develop a two-step “pop-in/pop-out” strategy to enrich cells that underwent homologous recombination (HR). This method provides a useful tool for studying telomerase biology, and suggests a general approach to edit loci with low targeting efficiency and to purify and visualize low abundance proteins.
As human Rap1, like its mouse and unicellular orthologs, affects gene expression, the authors propose that the conservation of Rap1 reflects its role in transcriptional regulation rather than a function at telomeres.
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To overcome the low CRISPR-Cas9 editing efficiency at the TERT locus, the scientists develop a two-step “pop-in/pop-out” strategy to enrich cells that underwent homologous recombination (HR). This method provides a useful tool for studying telomerase biology, and suggests a general approach to edit loci with low targeting efficiency and to purify and visualize low abundance proteins.
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