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The first Scube3 mutant mouse line with pleiotropic phenotypic alterations.
Genes Genomes Genetics G3 6, 4035-4046 (2016)
The vertebrate Scube (Signal peptide, CUB and EGF-like domain-containing protein) family consists of three independent members Scube1-3, which encode secreted cell surface-associated membrane glycoproteins. Limited information about the general function of this gene family is available, and their roles during adulthood. Here, we present the first Scube3 mutant mouse line (Scube3N294K/N294K) that clearly shows phenotypic alterations by carrying a missense mutation in exon 8, and thus contributes to understand SCUBE3 functions. We performed a detailed phenotypic characterization in the German Mouse Clinic (GMC). Scube3N294K/N294K mutants showed morphological abnormalities of the skeleton, alterations of parameters relevant for bone metabolism, changes in renal function and hearing impairments. These findings correlate with characteristics of the rare metabolic bone disorder Paget disease of bone (PDB), associated with the chromosomal region of human SCUBE3. In addition, alterations in energy metabolism, behavior and neurological functions were detected in Scube3N294K/N294K mice. The Scube3N294K/N294K mutant mouse line may serve as a new model for further studying the effect of impaired SCUBE3 gene function.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter SCUBE3; Paget disease of bone (PDB); mouse model; pleiotropy; systemic phenotype; Epithelial-mesenchymal Transition; Genome-wide Association; Pagets-disease; Calcium-metabolism; Marfan-syndrome; Kidney Injury; Lung-cancer; Rat-kidney; Cub Domain; Expression
e-ISSN 2160-1836
Zeitschrift Genes Genomes Genetics G3
Quellenangaben Band: 6, Heft: 12, Seiten: 4035-4046 Artikelnummer: , Supplement: ,
Verlag Genetics Society America
Verlagsort Pittsburgh, PA
Begutachtungsstatus peer-reviewed