PLoS ONE · 2012 · 159 citations · 27 references
Life SciencesBiotechnologyGeneticsDna RepairGenetic EngineeringGenome EditingError-prone MutagenesisMutagenesis StrategiesMutation InductionMutation ScreeningSite-directed MutagenesisZinc Finger NucleasesDeletion MutationsError-prone Dna RepairError-prone RepairMutagenesis ScreeningMutation RatesNucleasesSomatic MutationsTranscription Activator-like Effectors
Zinc Finger Nucleases (ZFNs) made by Context-Dependent Assembly (CoDA) and Transcription Activator-Like Effector Nucleases (TALENs) provide robust and user-friendly technologies for efficiently inactivating genes in zebrafish. These designer nucleases bind to and cleave DNA at particular target sites, inducing error-prone repair that can result in insertion or deletion mutations. Here, we assess the relative efficiencies of these technologies for inducing somatic DNA mutations in mosaic zebrafish. We find that TALENs exhibited a higher success rate for obtaining active nucleases capable of inducing mutations than compared with CoDA ZFNs. For example, all six TALENs tested induced DNA mutations at genomic target sites while only a subset of CoDA ZFNs exhibited detectable rates of mutagenesis. TALENs also exhibited higher mutation rates than CoDA ZFNs that had not been pre-screened using a bacterial two-hybrid assay, with DNA mutation rates ranging from 20%-76.8% compared to 1.1%-3.3%. Furthermore, the broader targeting range of TALENs enabled us to induce mutations at the methionine translation start site, sequences that were not targetable using the CoDA ZFN platform. TALENs exhibited similar toxicity to CoDA ZFNs, with >50% of injected animals surviving to 3 days of life. Taken together, our results suggest that TALEN technology provides a robust alternative to CoDA ZFNs for inducing targeted gene-inactivation in zebrafish, making it a preferred technology for creating targeted knockout mutants in zebrafish.
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Breaking the Code of DNA Binding Specificity of TAL-Type III Effectors
Jens Boch, Heidi Scholze, Sebastian Schornack et al. · Science · 2009 · 2.7K citations
A TALE nuclease architecture for efficient genome editing
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Targeting DNA Double-Strand Breaks with TAL Effector Nucleases
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