Evidence map›Paper›PMID 19474300›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Genetic evidence for shared mechanisms of epimorphic regeneration in zebrafish.

Zhao Qin, Linda K Barthel, Pamela A Raymond

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

92 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
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  8. Cell-Based Therapies for Glaucoma.Translational vision science & technology · 2023
    Article
  9. Article
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  11. Review
  12. Article
  13. Zebrafish models of inherited retinal dystrophies.Journal of translational genetics and genomics · 2022
    Article
  14. Article
  15. Review
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  17. Review
  18. Article
  19. Preparing a Single Cell Suspension from Zebrafish Retinal Tissue for Flow Cytometric Cell Sorting of Müller Glia.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2020
    Article
  20. Article

32 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

3 authors at 1 institution in 1 country.

Zhao QinDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan College of Literature, Science, and the Arts, 830 North University, Ann Arbor, MI 48109-1048, USA.
Linda K Barthel
Pamela A Raymond
University of Michigan–Ann Arbor · US

Funding

Vision Research CoreP30EY001730 · NEI · UNIVERSITY OF WASHINGTON · PI MAUREEN E NEITZ · 1985 to 2026
$23.5M
VIVARIUM MODULEP30EY007003 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David Antonetti · 1987 to 2026
$17.6M
NEW NEURONS IN THE RETINAR01EY004318 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAYMOND, PAMELA A · 1985 to 2010
$2.7M
NEI NIH HHS P30 EY001730NEI NIH HHS P30 EY007003NEI NIH HHS R01 EY004318
6 · The paper itself

Abstract

In a microarray-based gene profiling analysis of Müller glia-derived retinal stem cells in light-damaged retinas from adult zebrafish, we found that 2 genes required for regeneration of fin and heart tissues in zebrafish, hspd1 (heat shock 60-kDa protein 1) and mps1 (monopolar spindle 1), were up-regulated. Expression of both genes in the neurogenic Müller glia and progenitors was independently verified by quantitative reverse transcriptase PCR and in situ hybridization. Functional analysis of temperature-sensitive mutants of hspd1 and mps1 revealed that both are necessary for Müller glia-based cone photoreceptor regeneration in adult zebrafish retina. In the amputated fin, hspd1 is required for the induction of mesenchymal stem cells and blastema formation, whereas mps1 is required at a later step for rapid cell proliferation and outgrowth. This temporal sequence of hspd1 and mps1 function is conserved in the regenerating retina. Comparison of gene expression profiles from regenerating zebrafish retina, caudal fin, and heart muscle revealed additional candidate genes potentially implicated in injury-induced epimorphic regeneration in diverse zebrafish tissues.

Indexed as

RegenerationAnimalsChaperonin 60Gene Expression ProfilingLightNeurogliaPhotoreceptor Cells, VertebrateProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRetinal NeuronsStem Cell NicheStem CellsZebrafishZebrafish ProteinsChaperonin 60Protein Serine-Threonine KinasesProtein-Tyrosine Kinasesttk protein, zebrafishZebrafish Proteins

Identifiers

PMID19474300
PMCPMC2695073
OpenAlexW2138980520

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.