4 years ago

RNA targeting with CRISPR–Cas13

RNA targeting with CRISPR–Cas13
Aviv Regev, Julia Joung, Omar O. Abudayyeh, Daniel F. Voytas, Vanessa Verdine, Feng Zhang, Patrick Essletzbichler, Alice Y. Ting, David B. T. Cox, Shuo Han, Eric S. Lander, Max J. Kellner, Joseph J. Belanto, Jonathan S. Gootenberg

RNA has important and diverse roles in biology, but molecular tools to manipulate and measure it are limited. For example, RNA interference1,2,3 can efficiently knockdown RNAs, but it is prone to off-target effects4, and visualizing RNAs typically relies on the introduction of exogenous tags5. Here we demonstrate that the class 2 type VI6,7 RNA-guided RNA-targeting CRISPR–Cas effector Cas13a8 (previously known as C2c2) can be engineered for mammalian cell RNA knockdown and binding. After initial screening of 15 orthologues, we identified Cas13a from Leptotrichia wadei (LwaCas13a) as the most effective in an interference assay in Escherichia coli. LwaCas13a can be heterologously expressed in mammalian and plant cells for targeted knockdown of either reporter or endogenous transcripts with comparable levels of knockdown as RNA interference and improved specificity. Catalytically inactive LwaCas13a maintains targeted RNA binding activity, which we leveraged for programmable tracking of transcripts in live cells. Our results establish CRISPR–Cas13a as a flexible platform for studying RNA in mammalian cells and therapeutic development.

Publisher URL: http://dx.doi.org/10.1038/nature24049

DOI: 10.1038/nature24049

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