IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v526y2015i7571d10.1038_nature15254.html
   My bibliography  Save this article

Multiple mechanisms for CRISPR–Cas inhibition by anti-CRISPR proteins

Author

Listed:
  • Joseph Bondy-Denomy

    (University of Toronto
    †Present address: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, California 94158, USA.)

  • Bianca Garcia

    (University of Toronto)

  • Scott Strum

    (University of Toronto)

  • Mingjian Du

    (University of Toronto)

  • MaryClare F. Rollins

    (Montana State University)

  • Yurima Hidalgo-Reyes

    (University of Toronto)

  • Blake Wiedenheft

    (Montana State University)

  • Karen L. Maxwell

    (Donnelly Centre for Cellular and Biomolecular Research, University of Toronto)

  • Alan R. Davidson

    (University of Toronto
    University of Toronto)

Abstract

Bacterial cells evolved an immune system known as CRISPR–Cas to protect themselves from viral infection, triggering viruses to evolve anti-CRISPR proteins; here, three anti-CRISPR proteins are characterized, with each one interfering with the host CRISPR system at a different point.

Suggested Citation

  • Joseph Bondy-Denomy & Bianca Garcia & Scott Strum & Mingjian Du & MaryClare F. Rollins & Yurima Hidalgo-Reyes & Blake Wiedenheft & Karen L. Maxwell & Alan R. Davidson, 2015. "Multiple mechanisms for CRISPR–Cas inhibition by anti-CRISPR proteins," Nature, Nature, vol. 526(7571), pages 136-139, October.
  • Handle: RePEc:nat:nature:v:526:y:2015:i:7571:d:10.1038_nature15254
    DOI: 10.1038/nature15254
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature15254
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature15254?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Yanan Zhao & Jiaojiao Hu & Shan-Shan Yang & Jing Zhong & Jianping Liu & Shuo Wang & Yuzhuo Jiao & Fang Jiang & Ruiyang Zhai & Bingnan Ren & Hua Cong & Yuwei Zhu & Fengtong Han & Jixian Zhang & Yue Xu , 2022. "A redox switch regulates the assembly and anti-CRISPR activity of AcrIIC1," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    2. Mingfang Bi & Wenjing Su & Jiafu Li & Xiaobing Mo, 2024. "Insights into the inhibition of protospacer integration via direct interaction between Cas2 and AcrVA5," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:526:y:2015:i:7571:d:10.1038_nature15254. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.