Evidence map›Paper›PMID 24384391›Full record

ArticleDevelopmental biology2014

Dual function of Yap in the regulation of lens progenitor cells and cellular polarity.

Ji Yun Song, Raehee Park, Jin Young Kim, Lucinda Hughes, Li Lu, Seonhee Kim, Randy L Johnson, Seo-Hee Cho

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. The Hippo signalling pathway and its impact on eye diseases.Journal of cellular and molecular medicine · 2024
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Control of stem cell renewal and fate by YAP and TAZ.Nature reviews. Molecular cell biology · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Hippo Signaling in Embryogenesis and Development.Trends in biochemical sciences · 2021
    Review
  11. Review
  12. Heterozygous Loss of Yap1 in Mice Causes Progressive Cataracts.Investigative ophthalmology & visual science · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Hippo-yap signaling in ocular development and disease.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Review
  20. 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

8 authors at 3 institutions in 1 country.

Ji Yun SongShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States.
Raehee ParkShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States.
Jin Young KimShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States.
Lucinda HughesShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States.
Li LuDepartment of Biochemistry and Molecular Biology, University of Texas, M.D. Anderson Cancer Center, Houston, TX 77030, United States.
Seonhee KimShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States.
Randy L JohnsonDepartment of Biochemistry and Molecular Biology, University of Texas, M.D. Anderson Cancer Center, Houston, TX 77030, United States.
Seo-Hee ChoShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, United States. Electronic address: seo.hee.cho@temple.edu.
Temple University · USThe University of Texas MD Anderson Cancer Center · USTemple University Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Leber Congenital Amaurosis 8 models and pathogenic mechanismsR01EY020578 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHO, SEO-HEE · 2010 to 2022
$3.2M
Regulation Of Cortical Neurogenesis By Apical Complex ProteinsR01NS073112 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KIM, SEONHEE · 2010 to 2013
$1.3M
NCI NIH HHS P30 CA016672NEI NIH HHS EY020578NEI NIH HHS R01 EY020578NINDS NIH HHS R01 NS073112NINDS NIH HHS R01NS073112
6 · The paper itself

Abstract

Hippo-Yap signaling has been implicated in organ size determination via its regulation of cell proliferation, growth and apoptosis (Pan, 2007). The vertebrate lens comprises only two major cell types, lens progenitors and differentiated fiber cells, thereby providing a relatively simple system for studying size-controlling mechanisms. In order to investigate the role of Hippo-Yap signaling in lens size regulation, we conditionally ablated Yap in the developing mouse lens. Lens progenitor-specific deletion of Yap led to near obliteration of the lens primarily due to hypocellularity in the lens epithelium (LE) and accompanying lens fiber (LF) defects. A significantly reduced LE progenitor pool resulted mainly from failed self-renewal and increased apoptosis. Additionally, Yap-deficient lens progenitor cells precociously exited the cell cycle and expressed the LF marker, β-Crystallin. The mutant progenitor cells also exhibited multiple cellular and subcellular alterations including cell and nuclear shape change, organellar polarity disruption, and disorganized apical polarity complex and junction proteins such as Crumbs, Pals1, Par3 and ZO-1. Yap-deficient LF cells failed to anchor to the overlying LE layer, impairing their normal elongation and packaging. Furthermore, our localization study results suggest that, in the developing LE, Yap participates in the cell context-dependent transition from the proliferative to differentiation-competent state by integrating cell density information. Taken together, our results shed new light on Yap's indispensable and novel organizing role in mammalian organ size control by coordinating multiple events including cell proliferation, differentiation, and polarity.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsbeta-CrystallinsCell Cycle ProteinsCell PolarityCell ShapeDNA PrimersEpithelial CellsFluorescent Antibody TechniqueGene Expression Regulation, DevelopmentalHippo Signaling PathwayIn Situ HybridizationLens, CrystallineMicePhosphoproteinsProtein Serine-Threonine KinasesAdaptor Proteins, Signal Transducingbeta-CrystallinsCell Cycle ProteinsDNA PrimersPhosphoproteinsProtein Serine-Threonine KinasesYap1 protein, mouseYAP-Signaling ProteinsLensOrganogenesisOrgan size controlPolarityYap

Identifiers

PMID24384391
PMCPMC3985746
OpenAlexW2128088703

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.