Evidence map›Paper›PMID 30514786›Full record

ArticlemBio2018

Potent Cas9 Inhibition in Bacterial and Human Cells by AcrIIC4 and AcrIIC5 Anti-CRISPR Proteins.

Jooyoung Lee, Aamir Mir, Alireza Edraki, Bianca Garcia, Nadia Amrani, Hannah E Lou, Ildar Gainetdinov, April Pawluk, Raed Ibraheim, Xin D Gao and 4 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Bacterial immune systems.Antonie van Leeuwenhoek · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Mechanism of Cas9 inhibition by AcrIIA11.Nucleic acids research · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Rational Design of Enhanced Nme2Cas9 and Nme2bioRxiv : the preprint server for biology · 2024
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. CRISPR/Cas9 Landscape: Current State and Future Perspectives.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Keeping Cas9 out of the (R-)loop.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 2 countries.

Jooyoung Lee *RNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0003-4752-3792
Aamir Mir *RNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0003-0144-3914
Alireza EdrakiRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0003-0849-4888
Bianca GarciaDepartment of Biochemistry, University of Toronto, Toronto, Ontario, Canada.
Nadia AmraniRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0001-6871-7962
Hannah E LouRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Ildar GainetdinovRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0003-1719-043X
April PawlukDepartment of Biochemistry, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-6136-2086
Raed IbraheimRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0002-0961-7299
Xin D GaoRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0003-2917-2060
Pengpeng LiuDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID 0000-0002-4891-8780
Alan R DavidsonDepartment of Biochemistry, University of Toronto, Toronto, Ontario, Canada.
Karen L MaxwellDepartment of Biochemistry, University of Toronto, Toronto, Ontario, Canada karen.maxwell@utoronto.ca erik.sontheimer@umassmed.edu.ORCID 0000-0002-0211-5480
Erik J SontheimerRNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts, USA karen.maxwell@utoronto.ca erik.sontheimer@umassmed.edu.ORCID 0000-0002-0881-0310
University of Massachusetts Chan Medical School · USUniversity of Toronto · CA

Funding

Enhancing Genome Editing Technology with Natural Cas9 InhibitorsR01GM125797 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SONTHEIMER, ERIK J. · 2018 to 2021
$1.4M
CIHR FDN-15427CIHR PJT-152918NIGMS NIH HHS R01 GM125797
6 · The paper itself

Abstract

In their natural settings, CRISPR-Cas systems play crucial roles in bacterial and archaeal adaptive immunity to protect against phages and other mobile genetic elements, and they are also widely used as genome engineering technologies. Previously we discovered bacteriophage-encoded Cas9-specific anti-CRISPR (Acr) proteins that serve as countermeasures against host bacterial immunity by inactivating their CRISPR-Cas systems (A. Pawluk, N. Amrani, Y. Zhang, B. Garcia, et al., Cell 167:1829-1838.e9, 2016, https://doi.org/10.1016/j.cell.2016.11.017). We hypothesized that the evolutionary advantages conferred by anti-CRISPRs would drive the widespread occurrence of these proteins in nature (K. L. Maxwell, Mol Cell 68:8-14, 2017, https://doi.org/10.1016/j.molcel.2017.09.002; A. Pawluk, A. R. Davidson, and K. L. Maxwell, Nat Rev Microbiol 16:12-17, 2018, https://doi.org/10.1038/nrmicro.2017.120; E. J. Sontheimer and A. R. Davidson, Curr Opin Microbiol 37:120-127, 2017, https://doi.org/10.1016/j.mib.2017.06.003). We have identified new anti-CRISPRs using the same bioinformatic approach that successfully identified previous Acr proteins (A. Pawluk, N. Amrani, Y. Zhang, B. Garcia, et al., Cell 167:1829-1838.e9, 2016, https://doi.org/10.1016/j.cell.2016.11.017) against

Indexed as

CRISPR-Cas SystemsBacteriophagesClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Associated Protein 9Gene EditingHaemophilus parainfluenzaeHEK293 CellsHumansNeisseriaceaeViral ProteinsCRISPR-Associated Protein 9Viral Proteinsanti-CRISPRCas9CRISPRcrRNAtype II-C

Identifiers

PMID30514786
PMCPMC6282205
OpenAlexW2903404198

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.