Evidence map›Paper›PMID 20393120›Full record

ArticleInvestigative ophthalmology & visual science2010

Monoallelic expression of Krt12 gene during corneal-type epithelium differentiation of limbal stem cells.

Yasuhito Hayashi, Mindy K Call, Chia-Yang Liu, Miyuki Hayashi, George Babcock, Yuichi Ohashi, Winston W-Y Kao

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 30 citations in OpenAlex.

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  10. Sirt1 Regulates Corneal Epithelial Migration by Deacetylating Cortactin.Investigative ophthalmology & visual science · 2022
    Article
  11. Review
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  13. Lack of plakoglobin impairs integrity and wound healing in corneal epithelium in mice.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  14. Article
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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 3 institutions in 2 countries.

Yasuhito HayashiDepartment of Ophthalmology, University of Cincinnati, and Shriners Hospital for Children, Cincinnati, OH 45267-0838, USA.
Mindy K Call
Chia-Yang Liu
Miyuki Hayashi
George Babcock
Yuichi Ohashi
Winston W-Y Kao
Ehime University · JPShriners Hospitals for Children - Cincinnati · USUniversity of Cincinnati · US

Funding

STRUCTURE AND FUNCTION OF CORNEAL KERATIN K12 GENER01EY010556 · NEI · UNIVERSITY OF CINCINNATI · PI KAO, WINSTON W · 1995 to 2008
$2.2M
NEI NIH HHS EY 10556NEI NIH HHS R01 EY010556
6 · The paper itself

Abstract

purposeThe purpose of this study was to characterize a Krt12-Cre knock-in mouse line for corneal epithelium-specific gene ablation and to analyze the allelic selection of the keratin 12 (Krt12) gene during corneal type-epithelium differentiation.

methodsKnock-in mice were generated by gene targeting. The authors examined the expression patterns of several reporter genes in the corneas of bitransgenic Krt12cre/+/ROSA(EGFP), Krt12Cre/+/ZEG, and Krt12Cre/+/ZAP mouse lines. Krt12 and cre recombinase (Cre) immunostaining was performed. Corneal epithelial cells from bitransgenic Krt12Cre/+/ROSA(EGFP) mice were examined by fluorescence-activated cell sorter.

resultsMosaic and spiral expression patterns of EGFP were observed in young and adult bitransgenic Krt12Cre/+/ZEG mice, respectively. Immunostaining revealed that Cre- cells were also Krt12 negative in the corneal epithelia of Krt12Cre/-/ZAP mice. Using FACS analysis, 60% to 70% of the corneal epithelial cells from Krt12Cre/+/ROSAEGFP mice were EGFP positive, whereas 20% to 30% were negative. RT-PCR revealed that EGFP+ cells express both Krt12Cre and Krt12+ alleles, whereas EGFP- cells express only Krt12+. In the Krt12Cre/- cornea, the number of epithelial cells expressing Cre is the same as that found in Krt12Cre/Cre, which can be explained by the fragility of corneal epithelial cells that did not produce Krt12 because the Krt12Cre allele was not transcribed.

conclusionsThese observations are consistent with the notion that clonal limbal stem cells randomly activate Krt12 alleles in the process of terminal differentiation. The authors suggest that this selection is advantageous for retaining epithelial cells expressing the Krt12+ allele and that it allows tolerance to structural mutations of Krt12.

Indexed as

AllelesAnimalsCell DifferentiationEpithelial CellsEpithelium, CornealGene ExpressionGene Knock-In TechniquesGenes, ReporterGreen Fluorescent ProteinsKeratin-12Lac OperonLimbus CorneaeMiceMice, TransgenicMosaicismStem CellsGreen Fluorescent ProteinsKeratin-12KRT12 protein, mouse

Identifiers

PMID20393120
PMCPMC2941181
OpenAlexW1989404339

What OpenQuestion holds

Textmetadata
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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.