FIELD: biotechnology.
SUBSTANCE: methods are proposed for modifying a eukaryotic organism by manipulating a target sequence in a genome locus of interest by using the CRISPR-Cas system, as well as a method of treating or inhibiting a condition caused by a defect in a target sequence, and a composition containing components of said system.
EFFECT: present invention enables the change of genomic loci of the eukaryotic cell by using Cas9 nuclease fused with one or more nuclear localization sequences (NLS).
21 cl, 73 dwg, 35 tbl, 37 ex
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Authors
Dates
2020-05-18—Published
2013-12-12—Filed