A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity

Author:

Jinek Martin12,Chylinski Krzysztof34,Fonfara Ines4,Hauer Michael2,Doudna Jennifer A.1256,Charpentier Emmanuelle4

Affiliation:

1. Howard Hughes Medical Institute (HHMI), University of California, Berkeley, CA 94720, USA.

2. Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

3. Max F. Perutz Laboratories (MFPL), University of Vienna, A-1030 Vienna, Austria.

4. The Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, Department of Molecular Biology, Umeå University, S-90187 Umeå, Sweden.

5. Department of Chemistry, University of California, Berkeley, CA 94720, USA.

6. Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Abstract

Ditching Invading DNA Bacteria and archaea protect themselves from invasive foreign nucleic acids through an RNA-mediated adaptive immune system called CRISPR (clustered regularly interspaced short palindromic repeats)/CRISPR-associated (Cas). Jinek et al. (p. 816 , published online 28 June; see the Perspective by Brouns ) found that for the type II CRISPR/Cas system, the CRISPR RNA (crRNA) as well as the trans-activating crRNA—which is known to be involved in the pre-crRNA processing—were both required to direct the Cas9 endonuclease to cleave the invading target DNA. Furthermore, engineered RNA molecules were able to program the Cas9 endonuclease to cleave specific DNA sequences to generate double-stranded DNA breaks.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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