| Literature DB >> 29070703 |
David B T Cox1,2,3,4,5,6, Jonathan S Gootenberg1,2,3,4,7, Omar O Abudayyeh1,2,3,4,6, Brian Franklin1,2,3,4, Max J Kellner1,2,3,4, Julia Joung1,2,3,4, Feng Zhang8,2,3,4.
Abstract
Nucleic acid editing holds promise for treating genetic disease, particularly at the RNA level, where disease-relevant sequences can be rescued to yield functional protein products. Type VI CRISPR-Cas systems contain the programmable single-effector RNA-guided ribonuclease Cas13. We profiled type VI systems in order to engineer a Cas13 ortholog capable of robust knockdown and demonstrated RNA editing by using catalytically inactive Cas13 (dCas13) to direct adenosine-to-inosine deaminase activity by ADAR2 (adenosine deaminase acting on RNA type 2) to transcripts in mammalian cells. This system, referred to as RNA Editing for Programmable A to I Replacement (REPAIR), which has no strict sequence constraints, can be used to edit full-length transcripts containing pathogenic mutations. We further engineered this system to create a high-specificity variant and minimized the system to facilitate viral delivery. REPAIR presents a promising RNA-editing platform with broad applicability for research, therapeutics, and biotechnology.Entities:
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Year: 2017 PMID: 29070703 PMCID: PMC5793859 DOI: 10.1126/science.aaq0180
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728