Evidence map›Paper›PMID 35223827›Full record

ReviewFrontiers in cell and developmental biology2022

Efficient CRISPR Mutagenesis in Sturgeon Demonstrates Its Utility in Large, Slow-Maturing Vertebrates.

Jan Stundl, Vladimír Soukup, Roman Franěk, Anna Pospisilova, Viktorie Psutkova, Martin Pšenička, Robert Cerny, Marianne E Bronner, Daniel Meulemans Medeiros, David Jandzik

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2022. 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
1.1field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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 5 institutions in 3 countries.

Jan StundlDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Vladimír SoukupDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Roman FraněkSouth Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Faculty of Fisheries and Protection of Waters, University of South Bohemia in České Budějovice, Vodňany, Czechia.
Anna PospisilovaDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Viktorie PsutkovaDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Martin PšeničkaSouth Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Faculty of Fisheries and Protection of Waters, University of South Bohemia in České Budějovice, Vodňany, Czechia.
Robert CernyDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Marianne E BronnerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, United States.
Daniel Meulemans MedeirosDepartment of Ecology and Evolutionary Biology, University of Colorado in Boulder, Boulder, CO, United States.
David JandzikDepartment of Zoology, Faculty of Science, Charles University, Prague, Czechia.
Charles University · CZUniversity of South Bohemia in České Budějovice · CZCalifornia Institute of Technology · USComenius University Bratislava · SKUniversity of Colorado Boulder · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last decade, the CRISPR/Cas9 bacterial virus defense system has been adapted as a user-friendly, efficient, and precise method for targeted mutagenesis in eukaryotes. Though CRISPR/Cas9 has proven effective in a diverse range of organisms, it is still most often used to create mutant lines in lab-reared genetic model systems. However, one major advantage of CRISPR/Cas9 mutagenesis over previous gene targeting approaches is that its high efficiency allows the immediate generation of near-null mosaic mutants. This feature could potentially allow genotype to be linked to phenotype in organisms with life histories that preclude the establishment of purebred genetic lines; a group that includes the vast majority of vertebrate species. Of particular interest to scholars of early vertebrate evolution are several long-lived and slow-maturing fishes that diverged from two dominant modern lineages, teleosts and tetrapods, in the Ordovician, or before. These early-diverging or "basal" vertebrates include the jawless cyclostomes, cartilaginous fishes, and various non-teleost ray-finned fishes. In addition to occupying critical phylogenetic positions, these groups possess combinations of derived and ancestral features not seen in conventional model vertebrates, and thus provide an opportunity for understanding the genetic bases of such traits. Here we report successful use of CRISPR/Cas9 mutagenesis in one such non-teleost fish, sterlet

Indexed as

CRISPR/Cas9developmentevo-devoevolutionnon-teleost fishsturgeontargeted mutagenesisvertebrates

Identifiers

PMID35223827
PMCPMC8867083
OpenAlexW4211160633

What OpenQuestion holds

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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.