Literature DB >> 31775029

AcrIIA5 Inhibits a Broad Range of Cas9 Orthologs by Preventing DNA Target Cleavage.

Guoxu Song1, Fei Zhang1, Xuewen Zhang2, Xing Gao2, Xiaoxiao Zhu2, Dongdong Fan2, Yong Tian3.   

Abstract

CRISPR-Cas9 is an adaptive immune system for prokaryotes to defend against invasive genetic elements such as phages and has been used as a powerful tool for genome editing and modulation. To overcome CRISPR immunity, phages encode anti-CRISPR proteins (Acrs) to inhibit Cas9, providing an efficient "off-switch" tool for Cas9-based applications. Here, we characterized AcrIIA5, which is a Cas9 inhibitor discovered in a virulent phage of Streptococcus thermophilus. We found that AcrIIA5 is a potent and broad-spectrum inhibitor of CRISPR-Cas9, which can inhibit diverse Cas9 orthologs of type II-A, type II-B, and type II-C. AcrIIA5 inhibits Cas9 by preventing DNA target cleavage, but DNA target binding of Cas9 is unaffected. Importantly, it can affect the activity of the RuvC nuclease domain of Cas9 independent of the HNH nuclease domain. Our work expands the diversity of the inhibitory mechanisms used by Acrs and provides the guidance for developing controlling tools in Cas9-based applications.
Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  AcrIIA5; CRISPR-Cas9; anti-CRISPR; genome editing

Mesh:

Substances:

Year:  2019        PMID: 31775029     DOI: 10.1016/j.celrep.2019.10.078

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  7 in total

Review 1.  Structure-based functional mechanisms and biotechnology applications of anti-CRISPR proteins.

Authors:  Ning Jia; Dinshaw J Patel
Journal:  Nat Rev Mol Cell Biol       Date:  2021-06-04       Impact factor: 94.444

2.  Discovery of potent and versatile CRISPR-Cas9 inhibitors engineered for chemically controllable genome editing.

Authors:  Guoxu Song; Fei Zhang; Chunhong Tian; Xing Gao; Xiaoxiao Zhu; Dongdong Fan; Yong Tian
Journal:  Nucleic Acids Res       Date:  2022-03-21       Impact factor: 16.971

Review 3.  Type II anti-CRISPR proteins as a new tool for synthetic biology.

Authors:  Yadan Zhang; Mario Andrea Marchisio
Journal:  RNA Biol       Date:  2020-10-13       Impact factor: 4.652

4.  Computational design of anti-CRISPR proteins with improved inhibition potency.

Authors:  Jan Mathony; Zander Harteveld; Carolin Schmelas; Julius Upmeier Zu Belzen; Sabine Aschenbrenner; Wei Sun; Mareike D Hoffmann; Christina Stengl; Andreas Scheck; Sandrine Georgeon; Stéphane Rosset; Yanli Wang; Dirk Grimm; Roland Eils; Bruno E Correia; Dominik Niopek
Journal:  Nat Chem Biol       Date:  2020-04-13       Impact factor: 15.040

Review 5.  Small nucleic acids and the path to the clinic for anti-CRISPR.

Authors:  Christopher L Barkau; Daniel O'Reilly; Seth B Eddington; Masad J Damha; Keith T Gagnon
Journal:  Biochem Pharmacol       Date:  2021-02-27       Impact factor: 6.100

6.  Intrinsic disorder is essential for Cas9 inhibition of anti-CRISPR AcrIIA5.

Authors:  So Young An; Donghyun Ka; Iktae Kim; Eun-Hee Kim; Nak-Kyoon Kim; Euiyoung Bae; Jeong-Yong Suh
Journal:  Nucleic Acids Res       Date:  2020-07-27       Impact factor: 16.971

7.  Discovery of multiple anti-CRISPRs highlights anti-defense gene clustering in mobile genetic elements.

Authors:  Rafael Pinilla-Redondo; Saadlee Shehreen; Nicole D Marino; Robert D Fagerlund; Chris M Brown; Søren J Sørensen; Peter C Fineran; Joseph Bondy-Denomy
Journal:  Nat Commun       Date:  2020-11-06       Impact factor: 14.919

  7 in total

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