Evidence map›Paper›PMID 41526501›Full record

ArticleMolecular systems biology2026

Unlocking CRISPR-Cas9 editing for widely diverse Dictyostelid species.

Mireia Garriga-Canut, Nikki Cannon, Matt Benton, Andrea Zanon, Samuel T Horsfield, Jacob Scheurich, Kim Remans, John Lees, Alexandre Paix, Jordi van Gestel

Abstract read
In one paragraph

Article in Molecular systems biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

10 authors.

Mireia Garriga-CanutDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.ORCID http://orcid.org/0000-0002-5004-2802
Nikki CannonDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.ORCID http://orcid.org/0000-0001-7678-8146
Matt BentonDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.
Andrea ZanonDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.ORCID http://orcid.org/0000-0002-9261-5234
Samuel T HorsfieldEuropean Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Jacob ScheurichProtein Expression and Purification Core Facility, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.ORCID http://orcid.org/0000-0001-5982-7844
Kim RemansProtein Expression and Purification Core Facility, European Molecular Biology Laboratory, Heidelberg, 69117, Germany.ORCID http://orcid.org/0000-0002-4394-7953
John LeesEuropean Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.ORCID http://orcid.org/0000-0001-5360-1254
Alexandre PaixDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany. alexandre.paix@tuebingen.mpg.de.ORCID http://orcid.org/0000-0002-8080-7546
Jordi van GestelDevelopmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, 69117, Germany. jordi.vangestel@embl.de.ORCID http://orcid.org/0000-0001-5598-5239

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) 101116560
6 · The paper itself

Abstract

Dictyostelids are a species-rich clade of cellular slime molds that are widely found in soils and have been studied for over a century. Due to a lack of genome editing methods, most molecular research in Dictyostelids has focused on only a single species, Dictyostelium discoideum, which has severely limited broad-scale comparative analyses. Here, we introduce the first CRISPR-Cas9 editing approach that is cloning-free, selection-free, highly efficient, and effective across Dictyostelid species that diverged millions of years ago. Depending on the CRISPR-Cas9 target site, our editing approach generates knock-out efficiencies of up to 90% and knock-in efficiencies of up to 50% without a selective marker. We show that mutants can be isolated as soon as one day post-transfection, vastly outpacing existing methods for generating knock-outs, fusion proteins, and expression reporters. Leveraging single-cell sorting and fluorescent microscopy, we could readily apply our CRISPR-Cas9 editing approach to phylogenetically distant Dictyostelid species, including those that have never been genome edited before. Our methods therefore open the door to performing broad-scale genetic interrogations across the Dictyostelids.

Indexed as

CRISPR-Cas SystemsDictyosteliidaDictyosteliumGene EditingGene Knock-In TechniquesGene Knockout TechniquesMutationCell SortingCRISPR-Cas9DictyostelidsDictyostelium discoideumGenome Editing

Identifiers

PMID41526501
PMCPMC13046832

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.