Evidence map›Paper›PMID 36707549›Full record

ArticleScientific reports2023

Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping.

Ewa Sieliwonczyk, Bert Vandendriessche, Charlotte Claes, Evy Mayeur, Maaike Alaerts, Philip Holmgren, Tycho Canter Cremers, Dirk Snyders, Bart Loeys, Dorien Schepers

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Engineering precision zebrafish alleles of human disease.bioRxiv : the preprint server for biology · 2025
    Article
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  3. Review
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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

10 authors at 2 institutions in 2 countries.

Ewa SieliwonczykFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. ewa.sieliwonczyk@uantwerpen.be.
Bert VandendriesscheFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Charlotte ClaesFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Evy MayeurExperimental Neurobiology Unit, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Maaike AlaertsFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Philip HolmgrenFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Tycho Canter CremersFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Dirk SnydersExperimental Neurobiology Unit, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Bart LoeysFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Dorien SchepersFaculty of Medicine and Health Sciences, Center for Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
University of Antwerp · BERadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite numerous prior attempts to improve knock-in (KI) efficiency, the introduction of precise base pair substitutions by the CRISPR-Cas9 technique in zebrafish remains challenging. In our efforts to generate KI zebrafish models of human CACNA1C mutations, we have tested the effect of several CRISPR determinants on KI efficiency across two sites in a single gene and developed a novel method for early selection to ameliorate KI efficiency. We identified optimal KI conditions for Cas9 protein and non-target asymmetric PAM-distal single stranded deoxynucleotide repair templates at both cacna1c sites. An effect of distance to the cut site on the KI efficiency was only observed for a single repair template conformation at one of the two sites. By combining minimally invasive early genotyping with the zebrafish embryo genotyper (ZEG) device and next-generation sequencing, we were able to obtain an almost 17-fold increase in somatic editing efficiency. The added benefit of the early selection procedure was particularly evident for alleles with lower somatic editing efficiencies. We further explored the potential of the ZEG selection procedure for the improvement of germline transmission by demonstrating germline transmission events in three groups of pre-selected embryos.

Indexed as

CRISPR-Cas SystemsGene EditingAnimalsGenotypeHigh-Throughput Nucleotide SequencingHumansZebrafish

Identifiers

PMID36707549
PMCPMC9883431
OpenAlexW4318319308

What Socratic 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 Socratic graph.