2010/07/27 by Michelle Christian, Tomáš Čermák, Erin Doyle +5 · 9 citations
Biochemistry, Genetics and Molecular Biology · #CRISPR and Genetic Engineering #RNA Interference and Gene Delivery #Advanced biosensing and bioanalysis techniques
paper · pdf · doi:10.1534/genetics.110.120717
openalex publication_date 2010/07/27 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/22
Engineered nucleases that cleave specific DNA sequences in vivo are valuable reagents for targeted mutagenesis. Here we report a new class of sequence-specific nucleases created by fusing transcription activator-like effectors (TALEs) to the catalytic domain of the FokI endonuclease. Both native and custom TALE-nuclease fusions direct DNA double-strand breaks to specific, targeted sites.