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dCas13-mediated translational repression for accurate gene silencing in mammalian cells

Author

Listed:
  • Antonios Apostolopoulos

    (The University of Tokyo
    RIKEN Cluster for Pioneering Research)

  • Naohiro Kawamoto

    (RIKEN Cluster for Pioneering Research)

  • Siu Yu A. Chow

    (The University of Tokyo)

  • Hitomi Tsuiji

    (Aichi Gakuin University)

  • Yoshiho Ikeuchi

    (The University of Tokyo
    The University of Tokyo
    The University of Tokyo)

  • Yuichi Shichino

    (RIKEN Cluster for Pioneering Research)

  • Shintaro Iwasaki

    (The University of Tokyo
    RIKEN Cluster for Pioneering Research)

Abstract

Current gene silencing tools based on RNA interference (RNAi) or, more recently, clustered regularly interspaced short palindromic repeats (CRISPR)‒Cas13 systems have critical drawbacks, such as off-target effects (RNAi) or collateral mRNA cleavage (CRISPR‒Cas13). Thus, a more specific method of gene knockdown is needed. Here, we develop CRISPRδ, an approach for translational silencing, harnessing catalytically inactive Cas13 proteins (dCas13). Owing to its tight association with mRNA, dCas13 serves as a physical roadblock for scanning ribosomes during translation initiation and does not affect mRNA stability. Guide RNAs covering the start codon lead to the highest efficacy regardless of the translation initiation mechanism: cap-dependent, internal ribosome entry site (IRES)-dependent, or repeat-associated non-AUG (RAN) translation. Strikingly, genome-wide ribosome profiling reveals the ultrahigh gene silencing specificity of CRISPRδ. Moreover, the fusion of a translational repressor to dCas13 further improves the performance. Our method provides a framework for translational repression-based gene silencing in eukaryotes.

Suggested Citation

  • Antonios Apostolopoulos & Naohiro Kawamoto & Siu Yu A. Chow & Hitomi Tsuiji & Yoshiho Ikeuchi & Yuichi Shichino & Shintaro Iwasaki, 2024. "dCas13-mediated translational repression for accurate gene silencing in mammalian cells," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-46412-7
    DOI: 10.1038/s41467-024-46412-7
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    as
    1. Weiwei Cheng & Shaopeng Wang & Alexander A. Mestre & Chenglai Fu & Andres Makarem & Fengfan Xian & Lindsey R. Hayes & Rodrigo Lopez-Gonzalez & Kevin Drenner & Jie Jiang & Don W. Cleveland & Shuying Su, 2018. "C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    2. Shintaro Iwasaki & Stephen N. Floor & Nicholas T. Ingolia, 2016. "Rocaglates convert DEAD-box protein eIF4A into a sequence-selective translational repressor," Nature, Nature, vol. 534(7608), pages 558-561, June.
    3. Anna B. Loveland & Egor Svidritskiy & Denis Susorov & Soojin Lee & Alexander Park & Sarah Zvornicanin & Gabriel Demo & Fen-Biao Gao & Andrei A. Korostelev, 2022. "Ribosome inhibition by C9ORF72-ALS/FTD-associated poly-PR and poly-GR proteins revealed by cryo-EM," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    4. Alexandra East-Seletsky & Mitchell R. O’Connell & Spencer C. Knight & David Burstein & Jamie H. D. Cate & Robert Tjian & Jennifer A. Doudna, 2016. "Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection," Nature, Nature, vol. 538(7624), pages 270-273, October.
    5. Pekka Jaako & Alexandre Faille & Shengjiang Tan & Chi C. Wong & Norberto Escudero-Urquijo & Pablo Castro-Hartmann & Penny Wright & Christine Hilcenko & David J. Adams & Alan J. Warren, 2022. "eIF6 rebinding dynamically couples ribosome maturation and translation," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    6. Omar O. Abudayyeh & Jonathan S. Gootenberg & Patrick Essletzbichler & Shuo Han & Julia Joung & Joseph J. Belanto & Vanessa Verdine & David B. T. Cox & Max J. Kellner & Aviv Regev & Eric S. Lander & Da, 2017. "RNA targeting with CRISPR–Cas13," Nature, Nature, vol. 550(7675), pages 280-284, October.
    7. Kazuhiro Kashiwagi & Yuichi Shichino & Tatsuya Osaki & Ayako Sakamoto & Madoka Nishimoto & Mari Takahashi & Mari Mito & Friedemann Weber & Yoshiho Ikeuchi & Shintaro Iwasaki & Takuhiro Ito, 2021. "eIF2B-capturing viral protein NSs suppresses the integrated stress response," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    8. Zhipeng Ma & Peipei Zhu & Hui Shi & Liwei Guo & Qinghe Zhang & Yanan Chen & Shuming Chen & Zhe Zhang & Jinrong Peng & Jun Chen, 2019. "PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components," Nature, Nature, vol. 568(7751), pages 259-263, April.
    9. Laura Poliseno & Leonardo Salmena & Jiangwen Zhang & Brett Carver & William J. Haveman & Pier Paolo Pandolfi, 2010. "A coding-independent function of gene and pseudogene mRNAs regulates tumour biology," Nature, Nature, vol. 465(7301), pages 1033-1038, June.
    10. Thomas Becker & Sibylle Franckenberg & Stephan Wickles & Christopher J. Shoemaker & Andreas M. Anger & Jean-Paul Armache & Heidemarie Sieber & Charlotte Ungewickell & Otto Berninghausen & Ingo Daberko, 2012. "Structural basis of highly conserved ribosome recycling in eukaryotes and archaea," Nature, Nature, vol. 482(7386), pages 501-506, February.
    11. Ricardos Tabet & Laure Schaeffer & Fernande Freyermuth & Melanie Jambeau & Michael Workman & Chao-Zong Lee & Chun-Chia Lin & Jie Jiang & Karen Jansen-West & Hussein Abou-Hamdan & Laurent Désaubry & Ta, 2018. "CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
    12. Alexander J. Meeske & Sandra Nakandakari-Higa & Luciano A. Marraffini, 2019. "Cas13-induced cellular dormancy prevents the rise of CRISPR-resistant bacteriophage," Nature, Nature, vol. 570(7760), pages 241-245, June.
    13. Mohamed A. El-Brolosy & Zacharias Kontarakis & Andrea Rossi & Carsten Kuenne & Stefan Günther & Nana Fukuda & Khrievono Kikhi & Giulia L. M. Boezio & Carter M. Takacs & Shih-Lei Lai & Ryuichi Fukuda &, 2019. "Genetic compensation triggered by mutant mRNA degradation," Nature, Nature, vol. 568(7751), pages 193-197, April.
    14. Bo Zhang & Yangmiao Ye & Weiwei Ye & Vanja Perčulija & Han Jiang & Yiyang Chen & Yu Li & Jing Chen & Jinying Lin & Siqi Wang & Qi Chen & Yu-San Han & Songying Ouyang, 2019. "Two HEPN domains dictate CRISPR RNA maturation and target cleavage in Cas13d," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
    15. Malgorzata J. Latallo & Shaopeng Wang & Daoyuan Dong & Blake Nelson & Nathan M. Livingston & Rong Wu & Ning Zhao & Timothy J. Stasevich & Michael C. Bassik & Shuying Sun & Bin Wu, 2023. "Single-molecule imaging reveals distinct elongation and frameshifting dynamics between frames of expanded RNA repeats in C9ORF72-ALS/FTD," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
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