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  3. Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities.

Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities.

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DOI
10.48350/199680
Publisher DOI
10.1111/age.13467
PubMed ID
39136317
Abstract
Ichthyoses comprise a large heterogeneous group of skin disorders, characterized by generalized scaly and hyperkeratotic skin. We investigated a miniature poodle with early onset generalized scaling, dry and irregularly thickened skin, paw pad hyperkeratosis and abnormalities in hair and teeth. The clinical signs of ichthyosis were confirmed by histopathological examination, which revealed mild epidermal hyperplasia and lamellar orthokeratotic hyperkeratosis. A hereditary condition was suspected and a genetic investigation was initiated. We sequenced the whole genome of the affected dog and searched for potentially causative variants in functional candidate genes for the observed phenotype. The analysis revealed a heterozygous in-frame deletion in DSP, NC_049256.1:g.8804542_8804544del resulting from a de novo mutation event as evidenced by genotyping leukocyte DNA from both parents. The 3 bp deletion is predicted to remove one aspartic acid without disrupting the open reading frame (XM_038584124.1:c.1821_1823del, XP_038440052.1:p.(Asp608del)). The DSP gene encodes desmoplakin, a desmosomal plaque protein, responsible for cell-cell adhesion to provide resistance to mechanical stress in epidermal and cardiac tissues. We hypothesize that the deletion of one amino acid in the N-terminal globular head domain acts in a dominant negative manner and thus impairs the proper connection with other proteins. Several variants in DSP in humans and cattle have been described to result in different phenotypes associated with hair and skin abnormalities, sometimes in combination with variable cardiac and/or dental manifestations. In conclusion, we characterized a new syndromic ichthyosis phenotype in a dog and identified a de novo 3 bp deletion in the DSP gene as causal variant.
Date Issued
2024-10
Publication Type
Article
Subject(s)
500 Science > 590 Animals (Zoology)
600 Technology > 630 Agriculture
Subjects
Canis lupus familiaris dermatology dog genodermatosis precision medicine skin whole genome sequencing
Language(s)
en
Author(s)
Kiener, Sarah  
Institut für Genetik - Heimtiergenetik  
Institut für Genetik  
Lehner, Georg
Jagannathan, Vidya  
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institut für Genetik  
Welle, Monika Maria  
Institut für Tierpathologie (ITPA)  
Leeb, Tosso  orcid-logo
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institut für Genetik  
Additional Credits
Department of Clinical Research and Veterinary Public Health (DCR-VPH)  
Institut für Tierpathologie (ITPA)  
Institut für Genetik  
Institut für Genetik - Heimtiergenetik  
Journal
Animal genetics
Publisher
Wiley
ISSN
1365-2052
Access(Rights)
open.access
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