Evidence map›Paper›PMID 25231762›Full record

ArticleDevelopment (Cambridge, England)2014

Translational profiling through biotinylation of tagged ribosomes in zebrafish.

Michael P Housley, Sven Reischauer, Marc Dieu, Martine Raes, Didier Y R Stainier, Benoit Vanhollebeke

Abstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. CaOpen biology · 2025
    Article
  3. Article
  4. CXCR3-CXCL11 Signaling Restricts Angiogenesis and Promotes Pericyte Recruitment.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Trap-TRAP, a Versatile Tool for Tissue-Specific Translatomics in Zebrafish.Frontiers in cell and developmental biology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. 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

6 authors.

Michael P HousleyDepartment of Biochemistry & Biophysics, UCSF, San Francisco, CA 94158, USA michael.housley@mpi-bn.mpg.de didier.stainier@mpi-bn.mpg.de benoit.vanhollebeke@ulb.ac.be.
Sven ReischauerDepartment of Biochemistry & Biophysics, UCSF, San Francisco, CA 94158, USA.
Marc DieuURBC-Narilis, University of Namur, Namur B-5000, Belgium.
Martine RaesURBC-Narilis, University of Namur, Namur B-5000, Belgium.
Didier Y R StainierDepartment of Biochemistry & Biophysics, UCSF, San Francisco, CA 94158, USA michael.housley@mpi-bn.mpg.de didier.stainier@mpi-bn.mpg.de benoit.vanhollebeke@ulb.ac.be.
Benoit VanhollebekeDepartment of Biochemistry & Biophysics, UCSF, San Francisco, CA 94158, USA michael.housley@mpi-bn.mpg.de didier.stainier@mpi-bn.mpg.de benoit.vanhollebeke@ulb.ac.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterogeneity within a population of cells of the same type is a common theme in metazoan biology. Dissecting complex developmental and physiological processes crucially relies on our ability to probe the expression profile of these cell subpopulations. Current strategies rely on cell enrichment based on sequential or simultaneous use of multiple intersecting markers starting from a heterogeneous cell suspension. The extensive tissue manipulations required to generate single-cell suspensions, as well as the complexity of the required equipment, inherently complicate these approaches. Here, we propose an alternative methodology based on a genetically encoded system in the model organism Danio rerio (zebrafish). In transgenic fish, we take advantage of the combinatorial biotin transfer system, where polysome-associated mRNAs are selectively recovered from cells expressing both a tagged ribosomal subunit, Rpl10a, and the bacterial biotin ligase BirA. We have applied this technique to skeletal muscle development and identified new genes with interesting temporal expression patterns. Through this work we have thus developed additional tools for highly specific gene expression profiling.

Indexed as

Gene Expression ProfilingGene Expression Regulation, DevelopmentalTranscription, GeneticAnimalsAnimals, Genetically ModifiedBiotinylationCoenzyme A LigasesGreen Fluorescent ProteinsIn Situ HybridizationMass SpectrometryMuscle, SkeletalPolyribosomesRibosomal ProteinsRibosomesRNA-Binding ProteinsRNA, Messengerbiotin-CoA ligaseCoenzyme A LigasesGreen Fluorescent ProteinsRibosomal ProteinsRNA-Binding ProteinsRNA, MessengerRpl10a protein, zebrafishZebrafish ProteinsBirAGene expression profilingMuscle developmentTRAP

Identifiers

PMID25231762
PMCPMC4197690

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.