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RNA-guided human genome engineering via Cas9.

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      Abstract

      Bacteria and archaea have evolved adaptive immune defenses, termed clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) systems, that use short RNA to direct degradation of foreign nucleic acids. Here, we engineer the type II bacterial CRISPR system to function with custom guide RNA (gRNA) in human cells. For the endogenous AAVS1 locus, we obtained targeting rates of 10 to 25% in 293T cells, 13 to 8% in K562 cells, and 2 to 4% in induced pluripotent stem cells. We show that this process relies on CRISPR components; is sequence-specific; and, upon simultaneous introduction of multiple gRNAs, can effect multiplex editing of target loci. We also compute a genome-wide resource of ~190 K unique gRNAs targeting ~40.5% of human exons. Our results establish an RNA-guided editing tool for facile, robust, and multiplexable human genome engineering.

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      Affiliations
      [1 ] Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
      Journal
      Science
      Science (New York, N.Y.)
      American Association for the Advancement of Science (AAAS)
      1095-9203
      0036-8075
      Feb 15 2013
      : 339
      : 6121
      23287722 science.1232033 10.1126/science.1232033 3712628 NIHMS471334

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