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  3. Phloiokeratosis is a new ichthyosiform hyperkeratotic cornification disorder in dogs with SUV39H1 variants.

Phloiokeratosis is a new ichthyosiform hyperkeratotic cornification disorder in dogs with SUV39H1 variants.

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DOI
10.48620/99245
Publisher DOI
10.1038/s41598-026-59288-y
PubMed ID
42350566
Abstract
The continuous renewal of healthy epidermis depends on the finely regulated proliferation of basal keratinocytes and subsequent differentiation as the newly formed cells move upwards through the epidermis. Perturbations in keratinocyte differentiation may lead to cornification disorders. We investigated seven dogs from four independent families that showed striking multifocal tree bark-like skin lesions. Histopathologically, lesional skin was characterized by pronounced epidermal hyperkeratosis. We therefore tentatively termed the phenotype phloiokeratosis, derived from the Greek word phloiós for tree bark. Whole genome sequencing revealed four independent variants in the SUV39H1 gene encoding an H3K9 methyltransferase, which is involved in epigenetic silencing of chromatin. Phloiokeratosis is inherited as an X-chromosomal semi-dominant trait. Four of the affected dogs were heterozygous females and had lesion patterns reminiscent of Blaschko lines. In two of them, trio analyses experimentally confirmed de novo mutation events in the SUV39H1 gene. Previously, Suv39h1-/- knockout mice had been reported to have normal skin. So far, no human patients with SUV39H1 loss-of-function variants have been reported. The findings in SUV39H1 mutant dogs with phloiokeratosis for the first time link SUV39H1 deficiency to a heritable skin phenotype. Our study highlights the essential role of SUV39H1-mediated epigenetic silencing during normal keratinocyte differentiation.
Date Issued
2026
Publication Type
Article
Subject(s)
600 Technology > 630 Agriculture
Subjects
Canis lupus familiaris
•
Animal model
•
Dermatology
•
Epigenetics
•
Genodermatosis
•
Ichthyosis
•
Precision medicine
•
Skin
•
Whole genome sequencing
•
X chromosome
Language(s)
en
Author(s)
Kiener, Sarah  
Institut für Genetik - Heimtiergenetik  
Institute of Genetics  
Rietmann, Stefan J.  
Institut für Genetik - Heimtiergenetik  
Soto, Sara  
Institute of Animal Pathology, Laboratory Cancer Therapy Escape I
Institute of Animal Pathology, Teaching Diagnostics  
Institute of Animal Pathology  
Ramos, Sara J
Pucheu-Haston, Cherie M
Wu, Chi-Yen
Wheatcraft, Desirae
Simpson, Andrew
Åhman, Susanne
Wildermuth, Brett E
Drögemüller, Michaela  
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institute of Genetics  
Jagannathan, Vidhya  
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institute of Genetics  
Bradley, Charles W
Mauldin, Elizabeth A
Meertens, Nadine M
Welle, Monika  
Institute of Animal Pathology  
Leeb, Tosso  
Institute of Genetics  
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Additional Credits
Institute of Animal Pathology, Laboratory Cancer Therapy Escape I
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institut für Genetik - Heimtiergenetik  
Institute of Genetics  
Institute of Animal Pathology  
Institute of Animal Pathology, Teaching Diagnostics  
Department of Infectious Diseases and Pathobiology (DIP)  
Journal
Scientific Reports
Publisher
Nature Research
ISSN
2045-2322
Access(Rights)
open.access
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