Evidence map›Paper›PMID 32414936›Full record

ArticleDevelopment (Cambridge, England)2020

Targeted cell ablation in zebrafish using optogenetic transcriptional control.

Karen Mruk, Paulina Ciepla, Patrick A Piza, Mohammad A Alnaqib, James K Chen

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Tunable gene expression in zebrafish using RiboSCALE.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Journal of bacteriology · 2025
    Review
  6. Article
  7. Optogenetic Signaling Activation in Zebrafish Embryos.Journal of visualized experiments : JoVE · 2023
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Non-neuromodulatory Optogenetic Tools in Zebrafish.Frontiers in cell and developmental biology · 2020
    Review
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

5 authors at 2 institutions in 1 country.

Karen MrukDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA jameschen@stanford.edu kmruk@uwyo.edu.ORCID 0000-0003-4560-4951
Paulina CieplaDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-5139-9635
Patrick A PizaDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Mohammad A AlnaqibDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-6501-7976
James K ChenDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA jameschen@stanford.edu kmruk@uwyo.edu.ORCID 0000-0002-9220-8436
Stanford University · USUniversity of Wyoming · US

Funding

Zebrafish Models of CNS Injury and Locomotor RecoveryP20GM121310 · NIGMS · UNIVERSITY OF WYOMING · PI Rammohan Shukla · 2017 to 2026
$27.2M
Chemical tools for developmental biologyR35GM127030 · NIGMS · STANFORD UNIVERSITY · PI JAMES K CHEN · 2018 to 2026
$6.3M
NIGMS NIH HHS P20 GM121310NIGMS NIH HHS R35 GM127030
6 · The paper itself

Abstract

Cell ablation is a powerful method for elucidating the contributions of individual cell populations to embryonic development and tissue regeneration. Targeted cell loss in whole organisms has been typically achieved through expression of a cytotoxic or prodrug-activating gene product in the cell type of interest. This approach depends on the availability of tissue-specific promoters, and it does not allow further spatial selectivity within the promoter-defined region(s). To address this limitation, we have used the light-inducible GAVPO transactivator in combination with two genetically encoded cell-ablation technologies: the nitroreductase/nitrofuran system and a cytotoxic variant of the M2 ion channel. Our studies establish ablative methods that provide the tissue specificity afforded by

Indexed as

AnimalsAnimals, Genetically ModifiedAxonsBacterial ProteinsEmbryo, NonmammalianGene ExpressionGenes, ReporterLightMutagenesis, Site-DirectedNeuronsNitroreductasesOptogeneticsPromoter Regions, GeneticRimantadineViral Matrix ProteinsZebrafishBacterial ProteinsNitroreductasesRimantadineViral Matrix ProteinsCell ablationM2 ion channelNeural injuryNitroreductaseOptogeneticsZebrafish

Identifiers

PMID32414936
PMCPMC7328002
OpenAlexW3025942091

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.