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Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24

CRISPR-Cas systems are adaptive immune systems in bacteria and archaea that provide resistance against phages and other mobile genetic elements. To fight against CRISPR-Cas systems, phages and archaeal viruses encode anti-CRISPR (Acr) proteins that inhibit CRISPR-Cas systems. The expression of acr g...

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Autores principales: Kim, Gi Eob, Lee, So Yeon, Birkholz, Nils, Kamata, Kotaro, Jeong, Jae-Hee, Kim, Yeon-Gil, Fineran, Peter C, Park, Hyun Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638941/
https://www.ncbi.nlm.nih.gov/pubmed/36243977
http://dx.doi.org/10.1093/nar/gkac880
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author Kim, Gi Eob
Lee, So Yeon
Birkholz, Nils
Kamata, Kotaro
Jeong, Jae-Hee
Kim, Yeon-Gil
Fineran, Peter C
Park, Hyun Ho
author_facet Kim, Gi Eob
Lee, So Yeon
Birkholz, Nils
Kamata, Kotaro
Jeong, Jae-Hee
Kim, Yeon-Gil
Fineran, Peter C
Park, Hyun Ho
author_sort Kim, Gi Eob
collection PubMed
description CRISPR-Cas systems are adaptive immune systems in bacteria and archaea that provide resistance against phages and other mobile genetic elements. To fight against CRISPR-Cas systems, phages and archaeal viruses encode anti-CRISPR (Acr) proteins that inhibit CRISPR-Cas systems. The expression of acr genes is controlled by anti-CRISPR-associated (Aca) proteins encoded within acr-aca operons. AcrIF24 is a recently identified Acr that inhibits the type I-F CRISPR-Cas system. Interestingly, AcrIF24 was predicted to be a dual-function Acr and Aca. Here, we elucidated the crystal structure of AcrIF24 from Pseudomonas aeruginosa and identified its operator sequence within the regulated acr-aca operon promoter. The structure of AcrIF24 has a novel domain composition, with wing, head and body domains. The body domain is responsible for recognition of promoter DNA for Aca regulatory activity. We also revealed that AcrIF24 directly bound to type I-F Cascade, specifically to Cas7 via its head domain as part of its Acr mechanism. Our results provide new molecular insights into the mechanism of a dual functional Acr-Aca protein.
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spelling pubmed-96389412022-11-07 Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24 Kim, Gi Eob Lee, So Yeon Birkholz, Nils Kamata, Kotaro Jeong, Jae-Hee Kim, Yeon-Gil Fineran, Peter C Park, Hyun Ho Nucleic Acids Res Structural Biology CRISPR-Cas systems are adaptive immune systems in bacteria and archaea that provide resistance against phages and other mobile genetic elements. To fight against CRISPR-Cas systems, phages and archaeal viruses encode anti-CRISPR (Acr) proteins that inhibit CRISPR-Cas systems. The expression of acr genes is controlled by anti-CRISPR-associated (Aca) proteins encoded within acr-aca operons. AcrIF24 is a recently identified Acr that inhibits the type I-F CRISPR-Cas system. Interestingly, AcrIF24 was predicted to be a dual-function Acr and Aca. Here, we elucidated the crystal structure of AcrIF24 from Pseudomonas aeruginosa and identified its operator sequence within the regulated acr-aca operon promoter. The structure of AcrIF24 has a novel domain composition, with wing, head and body domains. The body domain is responsible for recognition of promoter DNA for Aca regulatory activity. We also revealed that AcrIF24 directly bound to type I-F Cascade, specifically to Cas7 via its head domain as part of its Acr mechanism. Our results provide new molecular insights into the mechanism of a dual functional Acr-Aca protein. Oxford University Press 2022-10-16 /pmc/articles/PMC9638941/ /pubmed/36243977 http://dx.doi.org/10.1093/nar/gkac880 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Structural Biology
Kim, Gi Eob
Lee, So Yeon
Birkholz, Nils
Kamata, Kotaro
Jeong, Jae-Hee
Kim, Yeon-Gil
Fineran, Peter C
Park, Hyun Ho
Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title_full Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title_fullStr Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title_full_unstemmed Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title_short Molecular basis of dual anti-CRISPR and auto-regulatory functions of AcrIF24
title_sort molecular basis of dual anti-crispr and auto-regulatory functions of acrif24
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638941/
https://www.ncbi.nlm.nih.gov/pubmed/36243977
http://dx.doi.org/10.1093/nar/gkac880
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