Evidence map›Paper›PMID 24555991›Full record

ReviewTrends in genetics : TIG2014

CRISPR-based technologies: prokaryotic defense weapons repurposed.

Rebecca M Terns, Michael P Terns

Abstract readReview
In one paragraph

Review in Trends in genetics : TIG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Review
  3. CRISPR-Cas systems in enterococci.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. CRISPR-Cas9/CRISPRi tools for cell factory construction in E. coli.World journal of microbiology & biotechnology · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Genomes in Focus: Development and Applications of CRISPR-Cas9 Imaging Technologies.Angewandte Chemie (International ed. in English) · 2018
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

2 authors at 1 institution in 1 country.

Rebecca M TernsDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.
Michael P TernsDepartment of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA; Department of Genetics, University of Georgia, Athens, GA 30602, USA; Department of Microbiology, University of Georgia, Athens, GA 30602, USA. Electronic address: mterns@bmb.uga.edu.
University of Georgia · US

Funding

Small RNA-based immunity by CRISPR-Cas complexes of Pyrococcus furiosusR01GM054682 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI TERNS, MICHAEL P, TERNS, REBECCA · 1997 to 2015
$4.8M
Delineation of CRISPR-Cas invader defense pathways in Streptococcus thermophilusR01GM099876 · NIGMS · UNIVERSITY OF GEORGIA · PI TERNS, MICHAEL P, TERNS, REBECCA · 2012 to 2015
$1.1M
NIGMS NIH HHS R01 GM054682NIGMS NIH HHS R01 GM099876NIGMS NIH HHS R01 GM54682NIGMS NIH HHS R01 GM99876
6 · The paper itself

Abstract

To combat potentially deadly viral infections, prokaryotic microbes enlist small RNA-based adaptive immune systems (CRISPR-Cas systems) that protect through sequence-specific recognition and targeted destruction of viral nucleic acids (either DNA or RNA depending on the system). Here, we summarize rapid progress made in redirecting the nuclease activities of these microbial immune systems to bind and cleave DNA or RNA targets of choice, by reprogramming the small guide RNAs of the various CRISPR-Cas complexes. These studies have demonstrated the potential of Type II CRISPR-Cas systems both as efficient and versatile genome-editing tools and as potent and specific regulators of gene expression in a broad range of cell types (including human) and organisms. Progress is also being made in developing a Type III RNA-targeting CRISPR-Cas system as a novel gene knockdown platform to investigate gene function and modulate gene expression for metabolic engineering in microbes.

Indexed as

Genetic TechniquesAnimalsClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsEndoribonucleasesHumansProkaryotic CellsRNA EditingEndoribonucleasesbiotechnologyCasCRISPRgenome editingmetabolic engineeringRNA silencing

Identifiers

PMID24555991
PMCPMC3981743
OpenAlexW2015607962

What OpenQuestion holds

Textmetadata
LicenceTDM
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.