Evidence map›Paper›PMID 35856642›Full record

ArticleThe CRISPR journal2022

Modulating CRISPR-Cas Genome Editing Using Guide-Complementary DNA Oligonucleotides.

Thomas Swartjes, Peng Shang, Dennis T M van den Berg, Tim Künne, Niels Geijsen, Stan J J Brouns, John van der Oost, Raymond H J Staals, Richard A Notebaart

Open access · hybridAbstract read
In one paragraph

Article in The CRISPR journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 93% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 3 institutions in 1 country.

Thomas SwartjesLaboratory of Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.ORCID 0000-0001-7528-5483
Peng ShangDepartment of Anatomy and Embryology, Leiden University Medical Centre, Leiden, The Netherlands; Delft, The Netherlands.
Dennis T M van den BergFood Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.
Tim KünneFood Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.
Niels GeijsenDepartment of Anatomy and Embryology, Leiden University Medical Centre, Leiden, The Netherlands; Delft, The Netherlands.
Stan J J BrounsDepartment of Bionanoscience, Delft University of Technology, Delft, The Netherlands; and Delft, The Netherlands.
John van der OostLaboratory of Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.ORCID 0000-0001-5024-1871
Raymond H J StaalsLaboratory of Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.ORCID 0000-0002-5741-9457
Richard A NotebaartFood Microbiology, Wageningen University and Research, Wageningen, The Netherlands; Delft, The Netherlands.ORCID 0000-0003-3469-1893
Wageningen University & Research · NLLeiden University Medical Center · NLDelft University of Technology · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) has revolutionized genome editing and has great potential for many applications, such as correcting human genetic disorders. To increase the safety of genome editing applications, CRISPR-Cas may benefit from strict control over Cas enzyme activity. Previously, anti-CRISPR proteins and designed oligonucleotides have been proposed to modulate CRISPR-Cas activity. In this study, we report on the potential of guide-complementary DNA oligonucleotides as controlled inhibitors of Cas9 ribonucleoprotein complexes. First, we show that DNA oligonucleotides inhibit Cas9 activity in human cells, reducing both on- and off-target cleavage. We then used

Indexed as

CRISPR-Cas SystemsGene EditingDNADNA, ComplementaryHumansOligonucleotidesDNADNA, ComplementaryOligonucleotides

Identifiers

PMID35856642
PMCPMC9419950
OpenAlexW4286231827

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.