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1.
Nat Commun ; 15(1): 1181, 2024 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-38360922

RESUMEN

Nucleobase editors represent an emerging technology that enables precise single-base edits to the genomes of eukaryotic cells. Most nucleobase editors use deaminase domains that act upon single-stranded DNA and require RNA-guided proteins such as Cas9 to unwind the DNA prior to editing. However, the most recent class of base editors utilizes a deaminase domain, DddAtox, that can act upon double-stranded DNA. Here, we target DddAtox fragments and a FokI-based nickase to the human CIITA gene by fusing these domains to arrays of engineered zinc fingers (ZFs). We also identify a broad variety of Toxin-Derived Deaminases (TDDs) orthologous to DddAtox that allow us to fine-tune properties such as targeting density and specificity. TDD-derived ZF base editors enable up to 73% base editing in T cells with good cell viability and favorable specificity.


Asunto(s)
Citidina Desaminasa , Edición Génica , Humanos , Citidina Desaminasa/genética , Citidina Desaminasa/metabolismo , ADN/metabolismo , Dedos de Zinc , Citidina/genética , Sistemas CRISPR-Cas
2.
Nat Commun ; 10(1): 1133, 2019 03 08.
Artículo en Inglés | MEDLINE | ID: mdl-30850604

RESUMEN

Genome editing for therapeutic applications often requires cleavage within a narrow sequence window. Here, to enable such high-precision targeting with zinc-finger nucleases (ZFNs), we have developed an expanded set of architectures that collectively increase the configurational options available for design by a factor of 64. These new architectures feature the functional attachment of the FokI cleavage domain to the amino terminus of one or both zinc-finger proteins (ZFPs) in the ZFN dimer, as well as the option to skip bases between the target triplets of otherwise adjacent fingers in each zinc-finger array. Using our new architectures, we demonstrate targeting of an arbitrarily chosen 28 bp genomic locus at a density that approaches 1.0 (i.e., efficient ZFNs available for targeting almost every base step). We show that these new architectures may be used for targeting three loci of therapeutic significance with a high degree of precision, efficiency, and specificity.


Asunto(s)
Desoxirribonucleasas de Localización Especificada Tipo II/genética , Edición Génica/métodos , Genoma Humano , Ingeniería de Proteínas/métodos , Nucleasas con Dedos de Zinc/genética , Emparejamiento Base , Secuencia de Bases , ARN Polimerasas Dirigidas por ADN/genética , ARN Polimerasas Dirigidas por ADN/metabolismo , Desoxirribonucleasas de Localización Especificada Tipo II/metabolismo , Escherichia coli/genética , Escherichia coli/metabolismo , Sitios Genéticos , Biblioteca Genómica , Humanos , Mutación INDEL , Células K562 , Biblioteca de Péptidos , Plásmidos/química , Plásmidos/metabolismo , Transformación Genética , Proteínas Virales/genética , Proteínas Virales/metabolismo , Nucleasas con Dedos de Zinc/metabolismo
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