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A versatile platform for locus-scale genome rewriting and verification

Routine rewriting of loci associated with human traits and diseases would facilitate their functional analysis. However, existing DNA integration approaches are limited in terms of scalability and portability across genomic loci and cellular contexts. We describe Big-IN, a versatile platform for tar...

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Detalles Bibliográficos
Autores principales: Brosh, Ran, Laurent, Jon M., Ordoñez, Raquel, Huang, Emily, Hogan, Megan S., Hitchcock, Angela M., Mitchell, Leslie A., Pinglay, Sudarshan, Cadley, John A., Luther, Raven D., Truong, David M., Boeke, Jef D., Maurano, Matthew T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958457/
https://www.ncbi.nlm.nih.gov/pubmed/33649239
http://dx.doi.org/10.1073/pnas.2023952118
Descripción
Sumario:Routine rewriting of loci associated with human traits and diseases would facilitate their functional analysis. However, existing DNA integration approaches are limited in terms of scalability and portability across genomic loci and cellular contexts. We describe Big-IN, a versatile platform for targeted integration of large DNAs into mammalian cells. CRISPR/Cas9-mediated targeting of a landing pad enables subsequent recombinase-mediated delivery of variant payloads and efficient positive/negative selection for correct clones in mammalian stem cells. We demonstrate integration of constructs up to 143 kb, and an approach for one-step scarless delivery. We developed a staged pipeline combining PCR genotyping and targeted capture sequencing for economical and comprehensive verification of engineered stem cells. Our approach should enable combinatorial interrogation of genomic functional elements and systematic locus-scale analysis of genome function.