Evidence map›Paper›PMID 24449846›Full record

ArticleDevelopment (Cambridge, England)2014

Targeted transgene integration overcomes variability of position effects in zebrafish.

Jennifer Anne Roberts, Irene Miguel-Escalada, Katherine Joan Slovik, Kathleen Theodora Walsh, Yavor Hadzhiev, Remo Sanges, Elia Stupka, Elizabeth Kate Marsh, Jorune Balciuniene, Darius Balciunas and 1 more

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cp36 serine recombinase as a new tool for zebrafish transgenesis.bioRxiv : the preprint server for biology · 2026
    Article
  5. A novelFrontiers in cell and developmental biology · 2026
    Article
  6. Article
  7. Article
  8. Article
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  10. Science advances · 2024
    Article
  11. Selective Cell Ablation Using an Improved Prodrug-Converting Nitroreductase.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  12. bioRxiv : the preprint server for biology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Heterogeneity and genomic loci of ubiquitous transgenic Cre reporter lines in zebrafish.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  18. Article
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Jennifer Anne RobertsSchool of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, B15 2TT, UK.
Irene Miguel-Escalada
Katherine Joan Slovik
Kathleen Theodora Walsh
Yavor Hadzhiev
Remo Sanges
Elia Stupka
Elizabeth Kate Marsh
Jorune Balciuniene
Darius Balciunas
Ferenc Müller
Temple University · US

Funding

Transposon-based Platform for Insertional Mutagenesis and Genome EngineeringR01HD061749 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI BALCIUNAS, DARIUS · 2010 to 2014
$1.5M
NICHD NIH HHS HD061749NICHD NIH HHS R01 HD061749
6 · The paper itself

Abstract

Zebrafish transgenesis is increasingly popular owing to the optical transparency and external development of embryos, which provide a scalable vertebrate model for in vivo experimentation. The ability to express transgenes in a tightly controlled spatio-temporal pattern is an important prerequisite for exploitation of zebrafish in a wide range of biomedical applications. However, conventional transgenesis methods are plagued by position effects: the regulatory environment of genomic integration sites leads to variation of expression patterns of transgenes driven by engineered cis-regulatory modules. This limitation represents a bottleneck when studying the precise function of cis-regulatory modules and their subtle variants or when various effector proteins are to be expressed for labelling and manipulation of defined sets of cells. Here, we provide evidence for the efficient elimination of variability of position effects by developing a PhiC31 integrase-based targeting method. To detect targeted integration events, a simple phenotype scoring of colour change in the lens of larvae is used. We compared PhiC31-based integration and Tol2 transgenesis in the analysis of the activity of a novel conserved enhancer from the developmentally regulated neural-specific esrrga gene. Reporter expression was highly variable among independent lines generated with Tol2, whereas all lines generated with PhiC31 into a single integration site displayed nearly identical, enhancer-specific reporter expression in brain nuclei. Moreover, we demonstrate that a modified integrase system can also be used for the detection of enhancer activity in transient transgenesis. These results demonstrate the power of the PhiC31-based transgene integration for the annotation and fine analysis of transcriptional regulatory elements and it promises to be a generally desirable tool for a range of applications, which rely on highly reproducible patterns of transgene activity in zebrafish.

Indexed as

Gene TargetingAnimalsAnimals, Genetically ModifiedBase SequenceBrainChromosomal Position EffectsEnhancer Elements, GeneticGene Expression RegulationGenes, ReporterGenetic LociGene Transfer TechniquesGenomeIntegrasesLens, CrystallineMolecular Sequence DataMutagenesis, InsertionalIntegrasesEnhancerIntegrasePosition effectsTol2TransgenesisZebrafish

Identifiers

PMID24449846
PMCPMC3899822
OpenAlexW2127478473

What OpenQuestion holds

Textmetadata
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.