Evidence map›Paper›PMID 25636444›Full record

ArticleGene expression patterns : GEP2015

Common and distinctive localization patterns of Crumbs polarity complex proteins in the mammalian eye.

Jin Young Kim, Ji Yun Song, Santi Karnam, Jun Young Park, Jamie J H Lee, Seonhee Kim, Seo-Hee Cho

Open access · greenAbstract read
In one paragraph

Article in Gene expression patterns : GEP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Family of Crumbs Genes and Human Disease.Molecular syndromology · 2016
    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

7 authors at 1 institution in 1 country.

Jin Young KimShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Ji Yun SongShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Santi KarnamShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Jun Young ParkShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Jamie J H LeeShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Seonhee KimShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Seo-Hee ChoShriners Hospitals Pediatric Research Center and Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA. Electronic address: seo.hee.cho@temple.edu.
Temple University · US

Funding

PHYSIOLOGY AND PHARMACOLOGY OF SYNAPSES IN THE RETINAR01EY004446 · NEI · BAYLOR COLLEGE OF MEDICINE · PI WU, SAMUEL M · 1985 to 2014
$5.4M
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
NEI NIH HHS EY020578NEI NIH HHS R01 EY004446NEI NIH HHS R01 EY020578NINDS NIH HHS NS073112NINDS NIH HHS R01 NS073112
6 · The paper itself

Abstract

Crumbs polarity complex proteins are essential for cellular and tissue polarity, and for adhesion of epithelial cells. In epithelial tissues deletion of any of three core proteins disrupts localization of the other proteins, indicating structural and functional interdependence among core components. Despite previous studies of function and co-localization that illustrated the properties that these proteins share, it is not known whether an individual component of the complex plays a distinct role in a unique cellular and developmental context. In order to investigate this question, we primarily used confocal imaging to determine the expression and subcellular localization of the core Crumbs polarity complex proteins during ocular development. Here we show that in developing ocular tissues core Crumbs polarity complex proteins, Crb, Pals1 and Patj, generally appear in an overlapping pattern with some exceptions. All three core complex proteins localize to the apical junction of the retinal and lens epithelia. Pals1 is also localized in the Golgi of the retinal cells and Patj localizes to the nuclei of the apically located subset of progenitor cells. These findings suggest that core Crumbs polarity complex proteins exert common and independent functions depending on cellular context.

Indexed as

Body PatterningAnimalsAnimals, NewbornEye ProteinsGolgi ApparatusHumansLens Cortex, CrystallineMCF-7 CellsMembrane ProteinsMiceNerve Tissue ProteinsNucleoside-Phosphate KinaseRetinaTight Junction ProteinsCrb1 protein, mouseCrb2 protein, mouseEye ProteinsMembrane ProteinsMpp5 protein, mouseNerve Tissue ProteinsNucleoside-Phosphate KinasePatj protein, mouseTight Junction ProteinsCrumbsCrumbs polarity complexLensPals1PatjRetina

Identifiers

PMID25636444
PMCPMC5033123
OpenAlexW2069080147

What OpenQuestion holds

Textmetadata
LicenceTDM
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.