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  3. Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
 

Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.

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BORIS DOI
10.7892/boris.82602
Date of Publication
May 2016
Publication Type
Article
Division/Institute

Institut für Genetik

Departement klinische...

Department of Clinica...

Author
Hytönen, Marjo K
Arumilli, Meharji
Lappalainen, Anu K
Owczarek, Marta
Institut für Genetik
Jagannathan, Vidya
Department of Clinical Research and Veterinary Public Health (DCR-VPH)
Hundi, Sruthi
Salmela, Elina
Venta, Patrick
Sarkiala, Eva
Jokinen, Tarja
Schweizer, Daniela Estherorcid-logo
Departement klinische Veterinärmedizin, Klinische Radiologie
Kere, Juha
Nieminen, Pekka
Drögemüller, Cordorcid-logo
Institut für Genetik
Lohi, Hannes
Subject(s)

500 - Science::590 - ...

600 - Technology::630...

500 - Science::570 - ...

600 - Technology::610...

Series
PLoS genetics
ISSN or ISBN (if monograph)
1553-7390
Publisher
Public Library of Science
Language
en
Publisher DOI
10.1371/journal.pgen.1006037
PubMed ID
27187611
Description
One to two percent of all children are born with a developmental disorder requiring pediatric hospital admissions. For many such syndromes, the molecular pathogenesis remains poorly characterized. Parallel developmental disorders in other species could provide complementary models for human rare diseases by uncovering new candidate genes, improving the understanding of the molecular mechanisms and opening possibilities for therapeutic trials. We performed various experiments, e.g. combined genome-wide association and next generation sequencing, to investigate the clinico-pathological features and genetic causes of three developmental syndromes in dogs, including craniomandibular osteopathy (CMO), a previously undescribed skeletal syndrome, and dental hypomineralization, for which we identified pathogenic variants in the canine SLC37A2 (truncating splicing enhancer variant), SCARF2 (truncating 2-bp deletion) and FAM20C (missense variant) genes, respectively. CMO is a clinical equivalent to an infantile cortical hyperostosis (Caffey disease), for which SLC37A2 is a new candidate gene. SLC37A2 is a poorly characterized member of a glucose-phosphate transporter family without previous disease associations. It is expressed in many tissues, including cells of the macrophage lineage, e.g. osteoclasts, and suggests a disease mechanism, in which an impaired glucose homeostasis in osteoclasts compromises their function in the developing bone, leading to hyperostosis. Mutations in SCARF2 and FAM20C have been associated with the human van den Ende-Gupta and Raine syndromes that include numerous features similar to the affected dogs. Given the growing interest in the molecular characterization and treatment of human rare diseases, our study presents three novel physiologically relevant models for further research and therapy approaches, while providing the molecular identity for the canine conditions.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/142240
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journal.pgen.1006037.PDFtextAdobe PDF2.81 MBAttribution (CC BY 4.0)publishedOpen
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