دورية أكاديمية

RNA-dependent RNA targeting by CRISPR-Cas9

التفاصيل البيبلوغرافية
العنوان: RNA-dependent RNA targeting by CRISPR-Cas9
المؤلفون: Strutt, Steven C, Torrez, Rachel M, Kaya, Emine, Negrete, Oscar A, Doudna, Jennifer A
المساهمون: National Science Foundation, Howard Hughes Medical Institute, German Academic Exchange Program, Laboratory Directed Research and Development, Paul Allen Frontiers Science Program
المصدر: eLife ; volume 7 ; ISSN 2050-084X
بيانات النشر: eLife Sciences Publications, Ltd
سنة النشر: 2018
المجموعة: eLife (E-Journal - via CrossRef)
الوصف: Double-stranded DNA (dsDNA) binding and cleavage by Cas9 is a hallmark of type II CRISPR-Cas bacterial adaptive immunity. All known Cas9 enzymes are thought to recognize DNA exclusively as a natural substrate, providing protection against DNA phage and plasmids. Here, we show that Cas9 enzymes from both subtypes II-A and II-C can recognize and cleave single-stranded RNA (ssRNA) by an RNA-guided mechanism that is independent of a protospacer-adjacent motif (PAM) sequence in the target RNA. RNA-guided RNA cleavage is programmable and site-specific, and we find that this activity can be exploited to reduce infection by single-stranded RNA phage in vivo. We also demonstrate that Cas9 can direct PAM-independent repression of gene expression in bacteria. These results indicate that a subset of Cas9 enzymes have the ability to act on both DNA and RNA target sequences, and suggest the potential for use in programmable RNA targeting applications.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.7554/elife.32724
الإتاحة: https://doi.org/10.7554/elife.32724Test
https://cdn.elifesciences.org/articles/32724/elife-32724-v2.pdfTest
https://cdn.elifesciences.org/articles/32724/elife-32724-v2.xmlTest
https://elifesciences.org/articles/32724Test
حقوق: http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.1D130BEB
قاعدة البيانات: BASE