Evidence map›Paper›PMID 23739135›Full record

ArticleDevelopment (Cambridge, England)2013

Polycomb repressive complex PRC2 regulates Xenopus retina development downstream of Wnt/β-catenin signaling.

Issam Aldiri, Kathryn B Moore, David A Hutcheson, Jianmin Zhang, Monica L Vetter

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Advances in the study of Müller glia reprogramming in mammals.Frontiers in cellular neuroscience · 2023
    Review
  4. Review
  5. Review
  6. Article
  7. Epigenetic regulation of retinal development.Epigenetics & chromatin · 2021
    Review
  8. Review
  9. Reprogramming Müller Glia to Regenerate Retinal Neurons.Annual review of vision science · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Issam AldiriDepartment of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.
Kathryn B Moore
David A Hutcheson
Jianmin Zhang
Monica L Vetter
University of Utah · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jun Yang · 2005 to 2026
$14.6M
REGULATION OF RETINAL NEUROGENESIS BY XATH5R01EY012274 · NEI · UNIVERSITY OF UTAH · PI VETTER, MONICA L · 1998 to 2021
$7.2M
NEI NIH HHS EY012274NEI NIH HHS P30 EY014800NEI NIH HHS R01 EY012274
6 · The paper itself

Abstract

The histone methyltransferase complex PRC2 controls key steps in developmental transitions and cell fate choices; however, its roles in vertebrate eye development remain unknown. Here, we report that in Xenopus, PRC2 regulates the progression of retinal progenitors from proliferation to differentiation. We show that the PRC2 core components are enriched in retinal progenitors and downregulated in differentiated cells. Knockdown of the PRC2 core component Ezh2 leads to reduced retinal progenitor proliferation, in part due to upregulation of the Cdk inhibitor p15(Ink4b). In addition, although PRC2 knockdown does not alter eye patterning, retinal progenitor gene expression or expression of the neural competence factor Sox2, it does cause suppression of proneural bHLH gene expression, indicating that PRC2 is crucial for the initiation of neural differentiation in the retina. Consistent with this, knocking down or blocking PRC2 function constrains the generation of most retinal neural cell types and promotes a Müller glial cell fate decision. We also show that Wnt/β-catenin signaling acting through the receptor Frizzled 5, but independent of Sox2, regulates expression of key PRC2 subunits in the developing retina. This is consistent with a role for this pathway in coordinating proliferation and the transition to neurogenesis in the Xenopus retina. Our data establish PRC2 as a regulator of proliferation and differentiation during eye development.

Indexed as

Wnt Signaling PathwayAnimalsCell DifferentiationCell ProliferationEnhancer of Zeste Homolog 2 ProteinFrizzled ReceptorsGene Knockdown TechniquesHistonesMethylationPolycomb Repressive Complex 2Repressor ProteinsRetinaXenopus laevisXenopus ProteinsEED protein, XenopusEnhancer of Zeste Homolog 2 ProteinEZH2 protein, XenopusFrizzled ReceptorsHistonesPolycomb Repressive Complex 2Repressor ProteinsSuz12 protein, XenopusXenopus ProteinsEpigeneticsEzh2Histone methylationNeurogenesisRetina developmentWnt signaling

Identifiers

PMID23739135
PMCPMC3699278
OpenAlexW2157826175

What Socratic 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 Socratic graph.