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Genome-wide CRISPR off-target prediction and optimization using RNA-DNA interaction fingerprints

Author

Listed:
  • Qinchang Chen

    (Tongji University
    Tongji University
    Zhejiang Lab)

  • Guohui Chuai

    (Tongji University
    Shanghai Research Institute for Intelligent Autonomous Systems)

  • Haihang Zhang

    (Chinese Academy of Agricultural Sciences)

  • Jin Tang

    (Zhejiang Lab)

  • Liwen Duan

    (Zhejiang Lab)

  • Huan Guan

    (Zhejiang Lab)

  • Wenhui Li

    (Zhejiang Lab)

  • Wannian Li

    (Tongji University)

  • Jiaying Wen

    (Tongji University)

  • Erwei Zuo

    (Chinese Academy of Agricultural Sciences)

  • Qing Zhang

    (China Innovation Center of Roche
    Ailomics Therapeutics)

  • Qi Liu

    (Tongji University
    Tongji University
    Zhejiang Lab
    Shanghai Research Institute for Intelligent Autonomous Systems)

Abstract

The powerful CRISPR genome editing system is hindered by its off-target effects, and existing computational tools achieved limited performance in genome-wide off-target prediction due to the lack of deep understanding of the CRISPR molecular mechanism. In this study, we propose to incorporate molecular dynamics (MD) simulations in the computational analysis of CRISPR system, and present CRISOT, an integrated tool suite containing four related modules, i.e., CRISOT-FP, CRISOT-Score, CRISOT-Spec, CRISORT-Opti for RNA-DNA molecular interaction fingerprint generation, genome-wide CRISPR off-target prediction, sgRNA specificity evaluation and sgRNA optimization of Cas9 system respectively. Our comprehensive computational and experimental tests reveal that CRISOT outperforms existing tools with extensive in silico validations and proof-of-concept experimental validations. In addition, CRISOT shows potential in accurately predicting off-target effects of the base editors and prime editors, indicating that the derived RNA-DNA molecular interaction fingerprint captures the underlying mechanisms of RNA-DNA interaction among distinct CRISPR systems. Collectively, CRISOT provides an efficient and generalizable framework for genome-wide CRISPR off-target prediction, evaluation and sgRNA optimization for improved targeting specificity in CRISPR genome editing.

Suggested Citation

  • Qinchang Chen & Guohui Chuai & Haihang Zhang & Jin Tang & Liwen Duan & Huan Guan & Wenhui Li & Wannian Li & Jiaying Wen & Erwei Zuo & Qing Zhang & Qi Liu, 2023. "Genome-wide CRISPR off-target prediction and optimization using RNA-DNA interaction fingerprints," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42695-4
    DOI: 10.1038/s41467-023-42695-4
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    1. Giulia I. Corsi & Kunli Qu & Ferhat Alkan & Xiaoguang Pan & Yonglun Luo & Jan Gorodkin, 2022. "CRISPR/Cas9 gRNA activity depends on free energy changes and on the target PAM context," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    2. Rongjie Fu & Wei He & Jinzhuang Dou & Oscar D. Villarreal & Ella Bedford & Helen Wang & Connie Hou & Liang Zhang & Yalong Wang & Dacheng Ma & Yiwen Chen & Xue Gao & Martin Depken & Han Xu, 2022. "Systematic decomposition of sequence determinants governing CRISPR/Cas9 specificity," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    3. Xiaoguang Pan & Kunli Qu & Hao Yuan & Xi Xiang & Christian Anthon & Liubov Pashkova & Xue Liang & Peng Han & Giulia I. Corsi & Fengping Xu & Ping Liu & Jiayan Zhong & Yan Zhou & Tao Ma & Hui Jiang & J, 2022. "Massively targeted evaluation of therapeutic CRISPR off-targets in cells," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    4. Brian J. Wainger & Matthew DeGennaro & Bina Santoro & Steven A. Siegelbaum & Gareth R. Tibbs, 2001. "Molecular mechanism of cAMP modulation of HCN pacemaker channels," Nature, Nature, vol. 411(6839), pages 805-810, June.
    5. Behrouz Eslami-Mossallam & Misha Klein & Constantijn V. D. Smagt & Koen V. D. Sanden & Stephen K. Jones & John A. Hawkins & Ilya J. Finkelstein & Martin Depken, 2022. "A kinetic model predicts SpCas9 activity, improves off-target classification, and reveals the physical basis of targeting fidelity," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    6. Kiran Musunuru & Alexandra C. Chadwick & Taiji Mizoguchi & Sara P. Garcia & Jamie E. DeNizio & Caroline W. Reiss & Kui Wang & Sowmya Iyer & Chaitali Dutta & Victoria Clendaniel & Michael Amaonye & Aar, 2021. "In vivo CRISPR base editing of PCSK9 durably lowers cholesterol in primates," Nature, Nature, vol. 593(7859), pages 429-434, May.
    7. Jessica T. Cortez & Elena Montauti & Eric Shifrut & Jovylyn Gatchalian & Yusi Zhang & Oren Shaked & Yuanming Xu & Theodore L. Roth & Dimitre R. Simeonov & Yana Zhang & Siqi Chen & Zhongmei Li & Jonath, 2020. "CRISPR screen in regulatory T cells reveals modulators of Foxp3," Nature, Nature, vol. 582(7812), pages 416-420, June.
    8. Matthew A. Coelho & Etienne Braekeleer & Mike Firth & Michal Bista & Sebastian Lukasiak & Maria Emanuela Cuomo & Benjamin J. M. Taylor, 2020. "CRISPR GUARD protects off-target sites from Cas9 nuclease activity using short guide RNAs," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
    9. Shiran Abadi & Winston X Yan & David Amar & Itay Mayrose, 2017. "A machine learning approach for predicting CRISPR-Cas9 cleavage efficiencies and patterns underlying its mechanism of action," PLOS Computational Biology, Public Library of Science, vol. 13(10), pages 1-24, October.
    10. Kyuho Han & Sarah E. Pierce & Amy Li & Kaitlyn Spees & Gray R. Anderson & Jose A. Seoane & Yuan-Hung Lo & Michael Dubreuil & Micah Olivas & Roarke A. Kamber & Michael Wainberg & Kaja Kostyrko & Marcus, 2020. "CRISPR screens in cancer spheroids identify 3D growth-specific vulnerabilities," Nature, Nature, vol. 580(7801), pages 136-141, April.
    11. Cong Huai & Gan Li & Ruijie Yao & Yingyi Zhang & Mi Cao & Liangliang Kong & Chenqiang Jia & Hui Yuan & Hongyan Chen & Daru Lu & Qiang Huang, 2017. "Structural insights into DNA cleavage activation of CRISPR-Cas9 system," Nature Communications, Nature, vol. 8(1), pages 1-9, December.
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