| Literature DB >> 32675376 |
Patrick Pausch1,2, Basem Al-Shayeb1,3, Ezra Bisom-Rapp4, Connor A Tsuchida1,5, Zheng Li6, Brady F Cress1,2, Gavin J Knott1,2,7, Steven E Jacobsen6,8, Jillian F Banfield1,9, Jennifer A Doudna10,2,8,11,12,13.
Abstract
CRISPR-Cas systems are found widely in prokaryotes, where they provide adaptive immunity against virus infection and plasmid transformation. We describe a minimal functional CRISPR-Cas system, comprising a single ~70-kilodalton protein, CasΦ, and a CRISPR array, encoded exclusively in the genomes of huge bacteriophages. CasΦ uses a single active site for both CRISPR RNA (crRNA) processing and crRNA-guided DNA cutting to target foreign nucleic acids. This hypercompact system is active in vitro and in human and plant cells with expanded target recognition capabilities relative to other CRISPR-Cas proteins. Useful for genome editing and DNA detection but with a molecular weight half that of Cas9 and Cas12a genome-editing enzymes, CasΦ offers advantages for cellular delivery that expand the genome editing toolbox.Entities:
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Year: 2020 PMID: 32675376 PMCID: PMC8207990 DOI: 10.1126/science.abb1400
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728