Evidence map›Paper›PMID 24820376›Full record

ArticleNature methods2014

Random and targeted transgene insertion in Caenorhabditis elegans using a modified Mos1 transposon.

Christian Frøkjær-Jensen, M Wayne Davis, Mihail Sarov, Jon Taylor, Stephane Flibotte, Matthew LaBella, Andrei Pozniakovsky, Donald G Moerman, Erik M Jorgensen

Abstract read
In one paragraph

Article in Nature methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 269 papers.

0numbers the graph read from it
0cells of the map it votes in
269citing 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

269 citing papers in PubMed.

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  13. Modular gene tagging inResearch square · 2026
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  20. Modular gene tagging inbioRxiv : the preprint server for biology · 2026
    Article

209 more citing papers are in PubMed but not listed here.

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

9 authors.

Christian Frøkjær-Jensen1] Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah, USA. [2] Department of Biology, University of Utah, Salt Lake City, Utah, USA. [3] Danish National Research Foundation Centre for Cardiac Arrhythmia, University of Copenhagen, Copenhagen, Denmark.ORCID 0000000231780906
M Wayne Davis1] Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah, USA. [2] Department of Biology, University of Utah, Salt Lake City, Utah, USA.
Mihail SarovTransgeneOmics, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Jon TaylorDepartment of Zoology, University of British Columbia, Vancouver, British Columbia, Canada.
Stephane FlibotteDepartment of Zoology, University of British Columbia, Vancouver, British Columbia, Canada.
Matthew LaBellaDepartment of Biology, University of Utah, Salt Lake City, Utah, USA.
Andrei PozniakovskyTransgeneOmics, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Donald G MoermanDepartment of Zoology, University of British Columbia, Vancouver, British Columbia, Canada.
Erik M Jorgensen1] Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah, USA. [2] Department of Biology, University of Utah, Salt Lake City, Utah, USA.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
Engineering the C. Elegans GenomeR01GM095817 · NIGMS · UNIVERSITY OF UTAH · PI JORGENSEN, ERIK M · 2011 to 2021
$2.8M
CIHRHoward Hughes Medical InstituteNIGMS NIH HHS 1R01GM095817NIGMS NIH HHS R01 GM095817NIGMS NIH HHS T32 GM007464NIH HHS P40 OD010440
6 · The paper itself

Abstract

We have generated a recombinant Mos1 transposon that can insert up to 45-kb transgenes into the Caenorhabditis elegans genome. The minimal Mos1 transposon (miniMos) is 550 bp long and inserts DNA into the genome at high frequency (~60% of injected animals). Genetic and antibiotic markers can be used for selection, and the transposon is active in C. elegans isolates and Caenorhabditis briggsae. We used the miniMos transposon to generate six universal Mos1-mediated single-copy insertion (mosSCI) landing sites that allow targeted transgene insertion with a single targeting vector into permissive expression sites on all autosomes. We also generated two collections of strains: a set of bright fluorescent insertions that are useful as dominant, genetic balancers and a set of lacO insertions to track genome position.

Indexed as

TransgenesAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansComparative Genomic HybridizationComputational BiologyDNA-Binding ProteinsDNA Transposable ElementsGenetic EngineeringGenetic MarkersGreen Fluorescent ProteinsModels, GeneticMutagenesis, InsertionalRecombinant ProteinsRecombination, GeneticTransposasesDNA-Binding ProteinsDNA Transposable ElementsGenetic MarkersGreen Fluorescent Proteinsmariner transposasesRecombinant ProteinsTransposases

Identifiers

PMID24820376
PMCPMC4126194

What OpenQuestion holds

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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.