Journal article Open Access
Pallarès-Masmitjà, Maria;
Ivančić, Dimitrije;
Mir-Pedrol, Júlia;
Jaraba-Wallace, Jessica;
Tagliani, Tommaso;
Oliva, Baldomero;
Rahmeh, Amal;
Sánchez-Mejías, Avencia;
Güell, Marc
{ "DOI": "10.1038/s41467-021-27183-x", "container_title": "Nature Communications", "title": "Find and cut-and-transfer (FiCAT) mammalian genome engineering", "issued": { "date-parts": [ [ 2021, 12, 3 ] ] }, "abstract": "<p><strong>Abstract</strong></p>\n\n<p>While multiple technologies for small allele genome editing exist, robust technologies for targeted integration of large DNA fragments in mammalian genomes are still missing. Here we develop a gene delivery tool (FiCAT) combining the precision of a CRISPR-Cas9 (find module), and the payload transfer efficiency of an engineered piggyBac transposase (cut-and-transfer module). FiCAT combines the functionality of Cas9 DNA scanning and targeting DNA, with piggyBac donor DNA processing and transfer capacity. PiggyBac functional domains are engineered providing increased on-target integration while reducing off-target events. We demonstrate efficient delivery and programmable insertion of small and large payloads in cellulo (human (Hek293T, K-562) and mouse (C2C12)) and in vivo in mouse liver. Finally, we evolve more efficient versions of FiCAT by generating a targeted diversity of 394,000 variants and undergoing 4 rounds of evolution. In this work, we develop a precise and efficient targeted insertion of multi kilobase DNA fragments in mammalian genomes.</p>", "author": [ { "family": "Pallar\u00e8s-Masmitj\u00e0,\u00a0Maria" }, { "family": "Ivan\u010di\u0107,\u00a0Dimitrije" }, { "family": "Mir-Pedrol,\u00a0J\u00falia" }, { "family": "Jaraba-Wallace,\u00a0Jessica" }, { "family": "Tagliani,\u00a0Tommaso" }, { "family": "Oliva,\u00a0Baldomero" }, { "family": "Rahmeh,\u00a0Amal" }, { "family": "S\u00e1nchez-Mej\u00edas,\u00a0Avencia" }, { "family": "G\u00fcell,\u00a0Marc" } ], "volume": "12", "type": "article-journal", "id": "6104372" }
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