Genome editing with designer nucleases such as TALEN and CRISPR/Cas enzymes has broad applications.
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Here the scientists report a simple and efficient method to visualize and quantify the efficiency of genomic mutations induced by genome-editing. Their approach is based on the expression of a two-color fusion protein in a vector that allows the insertion of the edited region in the genome in between the two color moieties. They show that this approach not only easily identifies developing animals with desired mutations but also efficiently quantifies the mutation rate in vivo. Furthermore, by using LacZα and GFP as the color moieties, this approach can even eliminate the need for a fluorescent microscope, allowing the analysis with simple bright field visualization. Such an approach will greatly simplify the screen for effective genome-editing enzymes and identify the desired mutant cells/animals.