Evidence map›Paper›PMID 42032034›Full record

ArticleScientific reports2026

Highly efficient genome editing using CRISPR/Cas9 ribonucleoprotein in the marine oleaginous diatom Fistulifera solaris.

Rein Yasui, Sawa Suzuki, Taiga Fujii, Yusuke Yabu, Yoshiaki Maeda, Satoshi Murata, Kosuke Kataoka, Tsuyoshi Tanaka

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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
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

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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.

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

8 authors.

Rein YasuiDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Sawa SuzukiDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Taiga FujiiDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Yusuke YabuDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Yoshiaki MaedaDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Satoshi MurataDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Kosuke KataokaDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan.
Tsuyoshi TanakaDivision of Biotechnology and Life Science, Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, 184-8588, Tokyo, Japan. tsuyo@cc.tuat.ac.jp.

Funding

a JSPS KAKENHI Grant-in-Aid for Scientific Research A 24H00392JSPS Program for Forming Japan's Peak Research Universities (J-PEAKS) JPJS00420230003the New Energy and Industrial Technology Development Organization JPNP17005
6 · The paper itself

Abstract

Microalgae are promising hosts for sustainable aviation fuel production due to their rapid growth and their advantage of not competing with agricultural crops. The oleaginous diatom Fistulifera solaris is notable for its exceptionally high lipid content. However, genetic engineering tools for this species remain limited, partly due to its allodiploid genome structure. Here, we report the successful development of a CRISPR/Cas9 genome editing method using ribonucleoprotein (RNP) complexes in F. solaris. We first targeted the adenine phosphoribosyl transferase (apt) genes as a selectable marker. Delivery of RNPs via particle bombardment to conserved regions of the two homoeologous apt genes resulted in 87% biallelic editing efficiency. Next, we demonstrated multiplex genome editing by co-targeting the apt genes and diadinoxanthin de-epoxidase (dde) genes as representative targets for improving valuable compound production in diatoms. Among 27 co-edited clones, 85% showed mutations in at least one dde homoeolog, and 63% exhibited biallelic mutations in both genes. This study demonstrates the applicability of RNP-mediated genome editing in diatoms. Furthermore, the success of this method suggests its broader applicability to non-model diatom species, providing a valuable tool for genome engineering in diatoms.

Indexed as

CRISPR-Cas SystemsDiatomsGene EditingRibonucleoproteinsAdenine PhosphoribosyltransferaseGenetic EngineeringMutationAdenine PhosphoribosyltransferaseRibonucleoproteins

Identifiers

PMID42032034
PMCPMC13276009

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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.