AcrIF9 tethers non-sequence specific dsDNA to the CRISPR RNA-guided surveillance complex
Marscha Hirschi,
Wang-Ting Lu,
Andrew Santiago-Frangos,
Royce Wilkinson,
Sarah M. Golden,
Alan R. Davidson (),
Gabriel C. Lander () and
Blake Wiedenheft ()
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Marscha Hirschi: The Scripps Research Institute
Wang-Ting Lu: University of Toronto
Andrew Santiago-Frangos: Montana State University
Royce Wilkinson: Montana State University
Sarah M. Golden: Montana State University
Alan R. Davidson: University of Toronto
Gabriel C. Lander: The Scripps Research Institute
Blake Wiedenheft: Montana State University
Nature Communications, 2020, vol. 11, issue 1, 1-6
Abstract:
Abstract Bacteria have evolved sophisticated adaptive immune systems, called CRISPR-Cas, that provide sequence-specific protection against phage infection. In turn, phages have evolved a broad spectrum of anti-CRISPRs that suppress these immune systems. Here we report structures of anti-CRISPR protein IF9 (AcrIF9) in complex with the type I-F CRISPR RNA-guided surveillance complex (Csy). In addition to sterically blocking the hybridization of complementary dsDNA to the CRISPR RNA, our results show that AcrIF9 binding also promotes non-sequence-specific engagement with dsDNA, potentially sequestering the complex from target DNA. These findings highlight the versatility of anti-CRISPR mechanisms utilized by phages to suppress CRISPR-mediated immune systems.
Date: 2020
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16512-1
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DOI: 10.1038/s41467-020-16512-1
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