tRNA anticodon cleavage by target-activated CRISPR-Cas13a effector.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
26 Apr 2024
Historique:
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 24 4 2024
Statut: ppublish

Résumé

Type VI CRISPR-Cas systems are among the few CRISPR varieties that target exclusively RNA. The CRISPR RNA-guided, sequence-specific binding of target RNAs, such as phage transcripts, activates the type VI effector, Cas13. Once activated, Cas13 causes collateral RNA cleavage, which induces bacterial cell dormancy, thus protecting the host population from the phage spread. We show here that the principal form of collateral RNA degradation elicited by

Identifiants

pubmed: 38657076
doi: 10.1126/sciadv.adl0164
doi:

Substances chimiques

RNA, Transfer 9014-25-9
Anticodon 0
CRISPR-Associated Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

eadl0164

Auteurs

Ishita Jain (I)

Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

Matvey Kolesnik (M)

Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.

Konstantin Kuznedelov (K)

Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

Leonid Minakhin (L)

Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

Natalia Morozova (N)

Peter the Great St. Petersburg Polytechnic University, Saint Petersburg, Russia.

Anna Shiriaeva (A)

Peter the Great St. Petersburg Polytechnic University, Saint Petersburg, Russia.
Saint Petersburg State University, Saint Petersburg, Russia.

Alexandr Kirillov (A)

Peter the Great St. Petersburg Polytechnic University, Saint Petersburg, Russia.

Sofia Medvedeva (S)

Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, Russia.

Alexei Livenskyi (A)

Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Moscow, Russia.
Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.

Laura Kazieva (L)

Institute of Biomedical Chemistry, Moscow, Russia.

Kira S Makarova (KS)

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health; Bethesda, MD, USA.

Eugene V Koonin (EV)

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health; Bethesda, MD, USA.

Sergei Borukhov (S)

Department of Cell Biology and Neuroscience, Rowan University School of Osteopathic Medicine at Stratford; Stratford, NJ, USA.

Konstantin Severinov (K)

Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Moscow, Russia.

Ekaterina Semenova (E)

Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.

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Classifications MeSH