Evidence map›Paper›PMID 41475352›Full record

ArticleCell reports methods2026

Efficient CRISPR-Cas genome editing in brown algae.

Cláudia Martinho, Masakazu Hoshino, Morgane Raphalen, Viktoriia Bukhanets, Anagha Kerur, Kenny A Bogaert, Rémy Luthringer, Susana M Coelho

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Germline fate determination by a single ARGONAUTE protein inProceedings of the National Academy of Sciences of the United States of America · 2026
    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

8 authors.

Cláudia MartinhoDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany; School of Life Sciences, University of Dundee, Division of Plant Sciences at The James Hutton Institute, Errol Road, DD2 5DA Dundee, UK. Electronic address: cmartinho001@dundee.ac.uk.
Masakazu HoshinoDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany; Research Center for Inland Seas, Kobe University, Rokkodai 1-1, Nadaku, Kobe 657-8501, Japan Kobe. Electronic address: mhoshino@harbor.kobe-u.ac.jp.
Morgane RaphalenDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany.
Viktoriia BukhanetsDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany.
Anagha KerurDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany.
Kenny A BogaertDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany.
Rémy LuthringerDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany.
Susana M CoelhoDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, 72076 Tübingen, Germany. Electronic address: susana.coelho@tuebingen.mpg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brown algae represent the third most complex lineage to have independently evolved multicellularity, distinct from plants and animals. Yet, functional studies of their development and evolution have been limited by the absence of efficient genome editing tools. Here, we present a robust, high-efficiency, and transgene-free CRISPR-based genome editing platform applicable across four ecologically and biotechnologically important brown algal species. Using Ectocarpus as a model, we optimized a polyethylene glycol (PEG)-mediated ribonucleoprotein (RNP) delivery system that achieves reproducible editing across multiple loci without cloning or specialized equipment. As proof of concept, we recreated the hallmark imm mutant phenotype by precisely editing the IMMEDIATE UPRIGHT (IMM) locus. APT/2-fluoroadenine (2-FA) selection further enhanced specificity with minimal false positives. The method was easily transferable to other species, including kelps. This platform now enables functional genomics in brown algae, providing powerful tools for investigating development, life cycle regulation, and the independent evolution of complex multicellularity.

Indexed as

CRISPR-Cas SystemsGene EditingPhaeophyceaePolyethylene GlycolsPolyethylene Glycolsbrown algaeCP: biotechnologyCRISPR-Casgenome editingRNP transfection

Identifiers

PMID41475352
PMCPMC12853178

What OpenQuestion holds

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Registered trials

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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.