Evidence map›Paper›PMID 31358806›Full record

ArticleScientific reports2019

Comparative genomics suggests loss of keratin K24 in three evolutionary lineages of mammals.

Florian Ehrlich, Maria Laggner, Lutz Langbein, Pamela Burger, Andreas Pollreisz, Erwin Tschachler, Leopold Eckhart

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  6. Inhibition of mTOR differently modulates planar and subepithelial fibrogenesis in human conjunctival fibroblasts.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
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  8. Decay of Skin-Specific Gene Modules in Pangolins.Journal of molecular evolution · 2023
    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.

Florian EhrlichResearch Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Maria LaggnerDepartment of Ophthalmology, Medical University of Vienna, Vienna, Austria.
Lutz LangbeinGerman Cancer Research Center, Department of Genetics of Skin Carcinogenesis, Heidelberg, Germany.
Pamela BurgerResearch Institute of Wildlife Ecology, University of Veterinary Medicine Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-6941-0257
Andreas PollreiszDepartment of Ophthalmology, Medical University of Vienna, Vienna, Austria.
Erwin TschachlerResearch Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Leopold EckhartResearch Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria. leopold.eckhart@meduniwien.ac.at.ORCID http://orcid.org/0000-0002-5645-2036
Medical University of Vienna · ATGerman Cancer Research Center · DEUniversity of Veterinary Medicine Vienna · AT

Funding

Austrian Science Fund FWF P 23801Austrian Science Fund FWF P 28004Austrian Science Fund FWF P 29623
6 · The paper itself

Abstract

Keratins are the main cytoskeletal proteins of epithelial cells and changes in the expression of keratins have contributed to the evolutionary adaptation of epithelia to different environments. Keratin K24 was proposed to be a differentiation marker of epidermal keratinocytes but the significance of K24 expression in the epidermis versus other tissues has remained elusive. Here, we show by RT-PCR, western blot, and immunofluorescence analyses that K24 is highly expressed in the epithelium of the cornea whereas its expression levels are significantly lower in other stratified epithelia including in the epidermis. To investigate the evolutionary history of K24, we screened the genome sequences of vertebrates for orthologs of the human KRT24 gene. The results of this comparative genomics study suggested that KRT24 originated in a common ancestor of amniotes and that it was lost independently in three clades of mammals, i.e. camels, cetaceans, and a subclade of pinnipeds comprising eared seals and the walrus. Together, the results of this study identify K24 as component of the cytoskeleton in the human corneal epithelium and reveal previously unknown differences of keratin gene content among mammalian species.

Indexed as

Evolution, MolecularPhylogenyAnimalsCorneaEpidermisHumansKeratins, Type IMammalsKeratins, Type I

Identifiers

PMID31358806
PMCPMC6662840
OpenAlexW2966445674

What OpenQuestion holds

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Registered trials

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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.