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Lack of Cas13a inhibition by anti-CRISPR proteins from Leptotrichia prophages

View ORCID ProfileAlexander J Meeske, View ORCID ProfileMatthew C. Johnson, View ORCID ProfileLogan T. Hille, View ORCID ProfileBenjamin P. Kleinstiver, View ORCID ProfileJoseph Bondy-Denomy
doi: https://doi.org/10.1101/2021.05.27.445852
Alexander J Meeske
1Department of Microbiology, University of Washington, Seattle, WA 98109, USA
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  • For correspondence: Meeske@uw.edu Joseph.Bondy-Denomy@ucsf.edu
Matthew C. Johnson
2Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94158, USA
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Logan T. Hille
3PhD Program in Biological and Biomedical Sciences, Harvard University, Boston, MA, 02115
4Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, 02114
5Department of Pathology, Massachusetts General Hospital, Boston, MA, 02114
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Benjamin P. Kleinstiver
4Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, 02114
5Department of Pathology, Massachusetts General Hospital, Boston, MA, 02114
6Department of Pathology, Harvard Medical School, Boston, MA, 02115
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Joseph Bondy-Denomy
2Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94158, USA
7Quantitative Biosciences Institute, University of California, San Francisco, San Francisco, CA 94158, USA
8Innovative Genomics Institute, Berkeley, CA 94720, USA
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  • For correspondence: Meeske@uw.edu Joseph.Bondy-Denomy@ucsf.edu
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Abstract

CRISPR systems are prokaryotic adaptive immune systems that use RNA-guided Cas nucleases to recognize and destroy foreign genetic elements, like bacteriophages and plasmids. To overcome CRISPR immunity, phages have evolved diverse families of anti-CRISPR proteins (Acrs), each of which inhibits the nucleic acid binding or cleavage activities of specific Cas protein families. Recently, Lin et al. (2020) described the discovery and characterization of 7 different Acr families (AcrVIA1-7) that inhibit type VI-A CRISPR systems, which use the nuclease Cas13a to perform RNA-guided RNA cleavage. In this Matters Arising article, we detail several inconsistencies that question the results reported in the Lin et al. (2020) study. These include inaccurate bioinformatics analyses, as well as reported experiments involving bacterial strains that are impossible to construct. The authors were unable to provide their published strains with which we might reproduce their experiments. We independently tested the Acr sequences described in Lin et al. (2020) in two different Cas13 inhibition assays, but could not detect anti-CRISPR activity. Taken together, our data and analyses prompt us to question the claim that AcrVIA1-7 reported in Lin et al. are bona fide type VI anti-CRISPR proteins.

Competing Interest Statement

Conflict of interest statement. J.B.-D. is a scientific advisory board member of SNIPR Biome and Excision Biotherapeutics and a scientific advisory board member and co-founder of Acrigen Biosciences. J.B.-D. is an inventor on patents filed by UCSF pertaining to anti-CRISPR technology. B.P.K is an inventor on patents and patent applications filed by Mass General Brigham that describe genome engineering technologies. B.P.K. consults for Avectas Inc., EcoR1 capital, and ElevateBio, and is an advisor to Acrigen Biosciences and Life Edit Therapeutics.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted May 27, 2021.
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Lack of Cas13a inhibition by anti-CRISPR proteins from Leptotrichia prophages
Alexander J Meeske, Matthew C. Johnson, Logan T. Hille, Benjamin P. Kleinstiver, Joseph Bondy-Denomy
bioRxiv 2021.05.27.445852; doi: https://doi.org/10.1101/2021.05.27.445852
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Lack of Cas13a inhibition by anti-CRISPR proteins from Leptotrichia prophages
Alexander J Meeske, Matthew C. Johnson, Logan T. Hille, Benjamin P. Kleinstiver, Joseph Bondy-Denomy
bioRxiv 2021.05.27.445852; doi: https://doi.org/10.1101/2021.05.27.445852

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