Ring nucleases deactivate type III CRISPR ribonucleases by degrading cyclic oligoadenylate
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41586-018-0557-5.pdf
Reference29 articles.
1. Mojica, F. J. & Rodriguez-Valera, F. The discovery of CRISPR in archaea and bacteria. FEBS J. 283, 3162–3169 (2016).
2. Makarova, K. S. et al. An updated evolutionary classification of CRISPR–Cas systems. Nat. Rev. Microbiol. 13, 722–736 (2015).
3. Jiang, F. & Doudna, J. A. The structural biology of CRISPR–Cas systems. Curr. Opin. Struct. Biol. 30, 100–111 (2015).
4. Niewoehner, O. et al. Type III CRISPR–Cas systems produce cyclic oligoadenylate second messengers. Nature 548, 543–548 (2017).
5. Kazlauskiene, M., Kostiuk, G., Venclovas, Č., Tamulaitis, G. & Siksnys, V. A cyclic oligonucleotide signaling pathway in type III CRISPR–Cas systems. Science 357, 605–609 (2017).
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