Evidence map›Paper›PMID 18406404›Full record

ArticleExperimental eye research2008

Lengsin expression and function during zebrafish lens formation.

Rachel L Harding, Sinéad Howley, Lee J Baker, Taylor R Murphy, William E Archer, Graeme Wistow, David R Hyde, Thomas S Vihtelic

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Proteome Profiling of Developing Murine Lens Through Mass Spectrometry.Investigative ophthalmology & visual science · 2018
    Article
  7. Article
  8. Article
  9. Review
  10. Dynamic reorganization of metabolic enzymes into intracellular bodies.Annual review of cell and developmental biology · 2012
    Review
  11. Article
  12. Article
  13. Toward a better understanding of human eye disease insights from the zebrafish, Danio rerio.Progress in molecular biology and translational science · 2011
    Review
  14. Article
  15. 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

8 authors at 2 institutions in 1 country.

Rachel L HardingUniversity of Notre Dame, Department of Biological Sciences and Center for Zebrafish Research, Galvin Life Science Center, Notre Dame, IN 46556-0369, USA.
Sinéad Howley
Lee J Baker
Taylor R Murphy
William E Archer
Graeme Wistow
David R Hyde
Thomas S Vihtelic
University of Notre Dame · USNational Institutes of Health · US

Funding

NEIBANK: EST Analysis/Bioinformatics for Ocular GenomicsZ01EY000320 · NEI · NATIONAL EYE INSTITUTE · PI WISTOW, GRAEME J · 1999 to 2008
$2.2M
Functional Analysis of Novel Genes in Eye Development and VisionZ01EY000433 · NEI · NATIONAL EYE INSTITUTE · PI WISTOW, GRAEME J · 2005 to 2008
$1.7M
Identification of Lens Development GenesR01EY014455 · NEI · UNIVERSITY OF NOTRE DAME · PI VIHTELIC, THOMAS S · 2003 to 2007
$1.3M
Intramural NIH HHS Z01 EY000320Intramural NIH HHS Z01 EY000433NEI NIH HHS R01 EY014455
6 · The paper itself

Abstract

A zebrafish ortholog of human lengsin was identified by EST analysis of an adult lens cDNA library. During zebrafish development, lengsin transcription is first detected at 24 h post-fertilization (hpf). Immunolocalization, using polyclonal antiserum generated against a Lengsin bacterial fusion protein, detects lens-specific protein in whole-mount embryos at 30 hpf. Lengsin expression in zebrafish follows the temporal expression of the alphaA- alphaB1- and betaB1-crystallin proteins in the lens. At 72 hpf, Lengsin is localized to a subpopulation of differentiating secondary fiber cells, while no expression is detected in the lens epithelial cells or central lens fibers. In the adult lens, Lengsin is restricted to a narrow band of cortical fibers and co-localizes with actin at the lateral faces of these interdigitating cells. Stable transgenic lines, using a 3 kb lengsin genomic fragment to regulate EGFP expression, recapitulate the Lengsin temporal and spatial expression patterns. Lengsin function in zebrafish lens formation was examined by antisense morpholino-mediated translation and mRNA splice inhibition. At 72 hpf, the lengsin morphant lenses are reduced in size and exhibit separations within the cortex due to defects in secondary fiber morphogenesis. The location of the morphant lens defects correlates with the Lengsin protein localization at this age. These results demonstrate Lengsin is required for proper fiber cell differentiation by playing roles in either cell elongation or the establishment of cell interactions.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationChick EmbryoCrystallinsDNA, ComplementaryFluorescent DyesGlutamate-Ammonia LigaseGreen Fluorescent ProteinsHumansLens, CrystallineMiceMicroscopy, ElectronOligonucleotides, AntisenseReverse Transcriptase Polymerase Chain ReactionSpecies SpecificityCrystallinsDNA, Complementaryenhanced green fluorescent proteinFluorescent DyesGlutamate-Ammonia LigaseGreen Fluorescent ProteinsOligonucleotides, Antisense

Identifiers

PMID18406404
PMCPMC2435080
OpenAlexW2075382919

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.