| Literature DB >> 29979968 |
Ryan Clarke1, Robert Heler2, Matthew S MacDougall1, Nan Cher Yeo3, Alejandro Chavez3, Maureen Regan4, Leslyn Hanakahi5, George M Church3, Luciano A Marraffini2, Bradley J Merrill6.
Abstract
The ability to target the Cas9 nuclease to DNA sequences via Watson-Crick base pairing with a single guide RNA (sgRNA) has provided a dynamic tool for genome editing and an essential component of adaptive immune systems in bacteria. After generating a double-stranded break (DSB), Cas9 remains stably bound to DNA. Here, we show persistent Cas9 binding blocks access to the DSB by repair enzymes, reducing genome editing efficiency. Cas9 can be dislodged by translocating RNA polymerases, but only if the polymerase approaches from one direction toward the Cas9-DSB complex. By exploiting these RNA-polymerase/Cas9 interactions, Cas9 can be conditionally converted into a multi-turnover nuclease, mediating increased mutagenesis frequencies in mammalian cells and enhancing bacterial immunity to bacteriophages. These consequences of a stable Cas9-DSB complex provide insights into the evolution of protospacer adjacent motif (PAM) sequences and a simple method of improving selection of highly active sgRNAs for genome editing.Entities:
Keywords: CRISPR; Cas9; DNA repair; RNA polymerase; genome editing; phage biology; strand bias; transcription
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Year: 2018 PMID: 29979968 PMCID: PMC6063522 DOI: 10.1016/j.molcel.2018.06.005
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970